{
 "publisher": "Consumer Sun",
 "data_as_of": "2026-10-14T04:58:55.691Z",
 "note": "Copied from official U.S. agency feeds without changes. The linked agency record is authoritative.",
 "feeds": [
  {
   "source": "cpsc",
   "label": "CPSC Recalls API",
   "ok": true,
   "records": 952,
   "feed_updated": null,
   "note": null
  },
  {
   "source": "fda",
   "label": "openFDA food enforcement",
   "ok": true,
   "records": 1365,
   "feed_updated": "2026-10-07",
   "note": null
  },
  {
   "source": "fda",
   "label": "openFDA drug enforcement",
   "ok": true,
   "records": 298,
   "feed_updated": "2026-10-07",
   "note": null
  },
  {
   "source": "fda",
   "label": "openFDA device enforcement",
   "ok": true,
   "records": 1087,
   "feed_updated": "2026-10-07",
   "note": null
  },
  {
   "source": "nhtsa",
   "label": "NHTSA recalls dataset",
   "ok": true,
   "records": 933,
   "feed_updated": null,
   "note": null
  },
  {
   "source": "fsis",
   "label": "USDA FSIS recalls (meat, poultry, eggs)",
   "ok": false,
   "records": 0,
   "feed_updated": null,
   "note": "Linked out: the FSIS API refuses requests from cloud servers."
  }
 ],
 "recalls": [
  {
   "agency": "CPSC",
   "recall_id": "27017",
   "date": "2026-10-08",
   "title": "Decathlon America Recalls Van Rysel GRVL AF Bicycles Due to Risk of Serious Injury or Death from Crash Hazard",
   "firm": "Decathlon America LLC, of San Francisco, California",
   "product": "Van Rysel GRVL AF Bicycles",
   "hazard": "The recalled bicycles' front lock nut can loosen during use, causing the front wheel to dislodge or loosen over time, posing a crash hazard.",
   "remedy": "Consumers should stop using the recalled bicycles immediately and take them to the nearest Recreational Equipment (REI Co-op) location for a free inspection and repair service of the front fork assembly. Anyone unable to visit an REI Co-op location can contact Decathlon Customer Service directly for assistance. Recalled models can be identified by the Van Rysel Product ID on the top right of the product label under the frame, beginning with the number 5.",
   "categories": [
    "home"
   ],
   "agency_url": "https://www.cpsc.gov/Recalls/2027/Decathlon-America-Recalls-Van-Rysel-GRVL-AF-Bicycles-Due-to-Risk-of-Serious-Injury-or-Death-from-Crash-Hazard",
   "url": "https://consumersun.com/recall/cpsc-27017-van-rysel-grvl-af-bicycles"
  },
  {
   "agency": "CPSC",
   "recall_id": "27016",
   "date": "2026-10-08",
   "title": "DR Power Equipment Recalls Pilot and Premier Trimmer Mowers Due to Risk of Serious Injury or Death from Fire and Burn Hazards",
   "firm": "Generac Power Systems Inc., of Waukesha, Wisconsin",
   "product": "DR Power Equipment Pilot and Premier Trimmer Mowers",
   "hazard": "Grass and debris can accumulate in the trimmer mowers and ignite, posing a risk of serious injury or death from fire and burn hazards.",
   "remedy": "Consumers should stop using the recalled trimmer mowers immediately and contact DR Power Equipment for a free repair kit. If consumers have concerns about installing the repair kit, contact DR Power Equipment to schedule a free repair installation from an authorized dealer.",
   "categories": [
    "home"
   ],
   "agency_url": "https://www.cpsc.gov/Recalls/2027/DR-Power-Equipment-Recalls-Pilot-and-Premier-Trimmer-Mowers-Due-to-Risk-of-Serious-Injury-or-Death-from-Fire-and-Burn-Hazards",
   "url": "https://consumersun.com/recall/cpsc-27016-pilot-and-premier-trimmer-mowers"
  },
  {
   "agency": "CPSC",
   "recall_id": "27015",
   "date": "2026-10-08",
   "title": "Giant Bicycle Recalls LED-Light Keys Included with SureLock Bike Lock Sets Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Consumer Products with Button Cell Batteries",
   "firm": "Giant Bicycle, Inc., of Newbury Park, California",
   "product": "LED-light bike lock keys",
   "hazard": "The LED-light key that was included with certain SureLock Bicycle Lock sets violates the mandatory safety standard for consumer products with button cell and coin batteries because the button batteries can be accessed easily by children, posing an ingestion hazard. Additionally, the packaging and product do not have the warnings required under Reese's Law. When button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns, and death.",
   "remedy": "Consumers should stop using the recalled LED-light key that was included with certain SureLock Bicycle Lock sets immediately and contact Giant Bicycle for a $5 refund. Consumers will be asked to bring the LED key to an authorized Giant retailer to participate in the recall and receive the refund. When returning the LED-light key to a retailer, consumers will be required to bring either the complete bicycle lock purchase or a picture of the serial number on the bicycle lock in order to verify the serial number is in the scope of the recall. Consumers may continue to use the bicycle lock and non-LED-light keys included with the SureLock Bicycle Lock sets. Note: Button and Coin cell batteries are hazardous. Batteries should be disposed of or recycled by following local hazardous waste procedures.",
   "categories": [
    "electronics",
    "home"
   ],
   "agency_url": "https://www.cpsc.gov/Recalls/2027/Giant-Bicycle-Recalls-LED-Light-Keys-Included-with-SureLock-Bike-Lock-Sets-Due-to-Risk-of-Serious-Injury-or-Death-from-Battery-Ingestion-Violates-Mandatory-Standard-for-Consumer-Products-with-Button-Cell-Batteries",
   "url": "https://consumersun.com/recall/cpsc-27015-led-light-keys-included-with-surelock-bike-lock"
  },
  {
   "agency": "CPSC",
   "recall_id": "27018",
   "date": "2026-10-08",
   "title": "ONTHEWEI Recalls Baby Bath Seats Due to Risk of Serious Injury or Death to Children from Drowning; Violate Mandatory Standard for Infant Bath Seats",
   "firm": "Hubei Youhong Trading Co., Ltd., dba ONTHEWEI, of China",
   "product": "ONTHEWEI Baby Bath Seats",
   "hazard": "The recalled bath seats violate the mandatory standard for infant bath seats because they are unstable and can tip over while in use, posing a risk of serious injury or death due to drowning.",
   "remedy": "Consumers should stop using the recalled bath seats immediately and contact ONTHEWEI for a full refund. Consumers will be asked to destroy the bath seat by writing in permanent marker \"RECALLED\" on the front of the bath seat, disassembling it by removing the back rest and arm restraints and cutting the three suction cups on the seat's underside and send a photo of the destroyed bath seat showing the marked product to onthewei@outlook.com. Consumers should then dispose of the recalled product.",
   "categories": [
    "baby"
   ],
   "agency_url": "https://cpsc.gov/Recalls/2027/ONTHEWEI-Recalls-Baby-Bath-Seats-Due-to-Risk-of-Serious-Injury-or-Death-to-Children-from-Drowning-Violate-Mandatory-Standard-for-Infant-Bath-Seats",
   "url": "https://consumersun.com/recall/cpsc-27018-baby-bath-seats"
  },
  {
   "agency": "CPSC",
   "recall_id": "27019",
   "date": "2026-10-08",
   "title": "Pacearth Direct Recalls PACEARTH Swing Seats Due to Risk of Serious Injury from Fall Hazard",
   "firm": "Pacearth Direct, of City of Industry, California",
   "product": "PACEARTH Swing Seats",
   "hazard": "The seats, metal carabiners or quick links, or webbing straps of the recalled swing seats can break during use, posing a risk of serious injury due to fall hazard.",
   "remedy": "Consumers should stop using the recalled swing seats immediately and contact Pacearth Direct for a full refund. Consumers will be asked to write \"RECALLED\" on the swing seat with permanent marker, take a photo of it, including the PACEARTH logo and email to recall@pacearth.com.",
   "categories": [
    "home"
   ],
   "agency_url": "https://www.cpsc.gov/Recalls/2027/Pacearth-Direct-Recalls-PACEARTH-Swing-Seats-Due-to-Risk-of-Serious-Injury-from-Fall-Hazard",
   "url": "https://consumersun.com/recall/cpsc-27019-pacearth-swing-seats"
  },
  {
   "agency": "CPSC",
   "recall_id": "27020",
   "date": "2026-10-08",
   "title": "Romorgniz Recalls Six-Drawer Dressers Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violate Mandatory Standard for Clothing Storage Units",
   "firm": "Zhangzhou Jinhao Sen Smart Home Co., Ltd., of China",
   "product": "Romorgniz Six-Drawer Dressers",
   "hazard": "The recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in risks of serious injuries or death to children. The dressers violate the mandatory safety standards as required by the STURDY Act.",
   "remedy": "Consumers should stop using the recalled dressers immediately if they are not anchored to the wall, place them in an area that children cannot access and contact Romorgniz for a full refund. Consumers will be asked to write in permanent marker \"RECALLED\" on the top, front and sides of the dresser, remove all drawers and send photos of the marked and disassembled dresser to Romorgnizrecall@outlook.com. Consumers should then dispose of the product.",
   "categories": [
    "home"
   ],
   "agency_url": "https://www.cpsc.gov/Recalls/2027/Romorgniz-Recalls-Six-Drawer-Dressers-Due-to-Risk-of-Serious-Injury-or-Death-from-Tip-Over-and-Entrapment-Hazards-Violate-Mandatory-Standard-for-Clothing-Storage-Units",
   "url": "https://consumersun.com/recall/cpsc-27020-six-drawer-dressers"
  },
  {
   "agency": "CPSC",
   "recall_id": "27021",
   "date": "2026-10-08",
   "title": "Snow Peak Recalls Propane Fireplace Inserts and Lava Rocks Due to Risk of Serious Injury or Death from Burn and Fire Hazards",
   "firm": "Snow Peak USA, Inc., of Portland, Oregon",
   "product": "Snow Peak Takibi Fireplace Propane Inserts and Lava Rocks",
   "hazard": "The fireplace's lava rocks can ignite and explode when heated in the propane insert, posing a risk of serious injury or death from burn and fire hazards.",
   "remedy": "Consumers should stop using the propane insert and lava rocks fireplace accessories immediately and contact Snow Peak for a full refund. Consumers will be provided with a prepaid shipping label to return the propane insert and lava rocks. For replacement lava rocks only, the consumer can keep the propane inserts, and the firm will ship replacement lava rocks to the consumer. Do not use inserts until replacement lava rocks are received. Consumers should dispose of the recalled lava rocks in accordance with any local and state ordinances.",
   "categories": [
    "home"
   ],
   "agency_url": "https://www.cpsc.gov/Recalls/2027/Snow-Peak-Recalls-Propane-Fireplace-Inserts-and-Lava-Rocks-Due-to-Risk-of-Serious-Injury-or-Death-from-Burn-and-Fire-Hazards",
   "url": "https://consumersun.com/recall/cpsc-27021-propane-fireplace-inserts-and-lava-rocks"
  },
  {
   "agency": "CPSC",
   "recall_id": "27022",
   "date": "2026-10-08",
   "title": "The Conqueror Recalls Avengers Medals Due to Risk of Serious Injury or Death from Magnet Ingestion; Violate Mandatory Standard for Magnets",
   "firm": "Actionary Limited, dba The Conqueror, of New Zealand",
   "product": "Avengers Infinity Gauntlet Medals",
   "hazard": "The recalled medals violate the mandatory safety standard for magnets because the high-powered magnets may detach, posing a deadly ingestion hazard to children. When high-powered magnets are swallowed, the ingested magnets can attract each other or other metal objects and become lodged in the digestive system. This can result in perforations, twisting, and/or blockage of the intestines, blood poisoning and death.",
   "remedy": "Consumers should stop using the Avengers Infinity Gauntlet Medal immediately and contact The Conqueror for instructions on receiving a full refund or a replacement medal. Consumers will be asked to cut the ribbon from the medal and write \"RECALLED\" in permanent marker on the medal and ribbon, throw the product away and email a photo of the disposed medal and ribbon to support@theconqueror.events.",
   "categories": [
    "baby"
   ],
   "agency_url": "https://www.cpsc.gov/Recalls/2027/The-Conqueror-Recalls-Avengers-Medals-Due-to-Risk-of-Serious-Injury-or-Death-from-Magnet-Ingestion-Violate-Mandatory-Standard-for-Magnets",
   "url": "https://consumersun.com/recall/cpsc-27022-avengers-medals"
  },
  {
   "agency": "FDA",
   "recall_id": "H-1407-2026",
   "date": "2026-10-07",
   "title": "TODD'S SEEDS LLC: Todd's Seeds Salad Sprouting Mixture - Broccoli recall",
   "firm": "TODD'S SEEDS LLC",
   "product": "Todd's Seeds Salad Sprouting Mixture - Broccoli, Mustard, Alfalfa and Cabbage, packaged in heat-sealed resealable bags in the following sizes: 1/4 lb., 1/2 lb., and 1 lb.",
   "hazard": "Products contain alfalfa seed recalled by the supplier and may be contaminated with E. coli and/or Salmonella (downstream recall)",
   "remedy": null,
   "categories": [
    "food"
   ],
   "agency_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-1407-2026%22",
   "url": "https://consumersun.com/recall/fda-h-1407-2026-todd-s-seeds-llc-todd-s-seeds-salad-sprouting"
  },
  {
   "agency": "FDA",
   "recall_id": "H-1402-2026",
   "date": "2026-10-07",
   "title": "Galil Importing Corp: Lior brand Cinnamon Ground Seasoning recall",
   "firm": "Galil Importing Corp",
   "product": "Lior brand Cinnamon Ground Seasoning; 90g transparent plastic container; UPC 794711005484.",
   "hazard": "Product contains elevated levels of lead.",
   "remedy": null,
   "categories": [
    "food"
   ],
   "agency_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-1402-2026%22",
   "url": "https://consumersun.com/recall/fda-h-1402-2026-galil-importing-corp-lior-brand-cinnamon-ground"
  },
  {
   "agency": "FDA",
   "recall_id": "H-1399-2026",
   "date": "2026-10-07",
   "title": "LMSI, LLC: Kofinas Garlic Mediterranean Infused Extra Virgin Olive Oil recall",
   "firm": "LMSI, LLC",
   "product": "Kofinas Garlic Mediterranean Infused Extra Virgin Olive Oil, packaged in 3.4 fl oz (100mL), 8.5 fl oz (250mL), and 17 fl oz (500mL) glass bottles, UPC: 799475717185 (on 8.5 fl oz/250mL), 799475717178 (on 17 fl oz/500mL). The 3.4 fl oz/100mL bottles were sold as part of a gift set; the 8.5 fl oz/250mL and 17 fl oz/500mL products were sold individually.",
   "hazard": "Product contains garlic essential oil not approved for culinary use",
   "remedy": null,
   "categories": [
    "food"
   ],
   "agency_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-1399-2026%22",
   "url": "https://consumersun.com/recall/fda-h-1399-2026-lmsi-llc-kofinas-garlic-mediterranean-infused"
  },
  {
   "agency": "FDA",
   "recall_id": "H-1397-2026",
   "date": "2026-10-07",
   "title": "Admiral Beverage Corporation: 7up Tropical beverage recall",
   "firm": "Admiral Beverage Corporation",
   "product": "7up Tropical beverage, shelf stable, 12oz can in a 12pk wrap, labeled as 7 up Tropical Beverage containing cans that are labeled as 7Up Tropical Zero Sugar which contain full sugar soda. 12 fl oz, UPC: 0 78000 03798 2, Dr Pepper/Seven Up, Inc., 6425 Hall of Fame Lane, Frisco TX 75034.",
   "hazard": "Product may contain undeclared sugar.",
   "remedy": null,
   "categories": [
    "food"
   ],
   "agency_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-1397-2026%22",
   "url": "https://consumersun.com/recall/fda-h-1397-2026-admiral-beverage-corporation-7up-tropical-beverage"
  },
  {
   "agency": "FDA",
   "recall_id": "H-1405-2026",
   "date": "2026-10-07",
   "title": "TODD'S SEEDS LLC: Todd's Seeds Broccoli & Friends Sprouting Seed Mix - Broccoli recall",
   "firm": "TODD'S SEEDS LLC",
   "product": "Todd's Seeds Broccoli & Friends Sprouting Seed Mix - Broccoli, Alfalfa, Radish, Clover, packaged in 1 oz. sample packets and heat-sealed resealable bags in the following sizes: 1/4 lb., 1/2 lb., 1 lb., 2.5 lb., and 5 lb.",
   "hazard": "Products contain alfalfa seed recalled by the supplier and may be contaminated with E. coli and/or Salmonella (downstream recall)",
   "remedy": null,
   "categories": [
    "food"
   ],
   "agency_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-1405-2026%22",
   "url": "https://consumersun.com/recall/fda-h-1405-2026-todd-s-seeds-llc-todd-s-seeds-broccoli-and"
  },
  {
   "agency": "FDA",
   "recall_id": "H-1403-2026",
   "date": "2026-10-07",
   "title": "Coco G's Snack Foods, Inc.: Coco G's Courmet Flaming Cheddar Hots recall",
   "firm": "Coco G's Snack Foods, Inc.",
   "product": "Coco G's Courmet Flaming Cheddar Hots, Spicy Cheddar Cheese Popcorn. Packaged in the following sized plastic bags: 1. 2.5 oz (81g), UPC 6 94161-25911 9. 2. 4.15 oz (118g), UPC 6 94161-38911 3. 3. 5 oz (142g), UPC 6 94161-60005 8. 761 Commerce Dr. Unit F, Union Grove, WI 53182",
   "hazard": "Potential Salmonella contamination.",
   "remedy": null,
   "categories": [
    "food"
   ],
   "agency_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-1403-2026%22",
   "url": "https://consumersun.com/recall/fda-h-1403-2026-coco-g-s-snack-foods-inc-coco-g-s-courmet-flaming"
  },
  {
   "agency": "FDA",
   "recall_id": "H-1398-2026",
   "date": "2026-10-07",
   "title": "Salata Dressings, LLC: Salata Salad Kitchen Jalapen¿o Avocado Dressing recall",
   "firm": "Salata Dressings, LLC",
   "product": "Salata Salad Kitchen Jalapen¿o Avocado Dressing. Keep Refrigerated. Packaged in the following sizes: 1. 12.5 fl. oz. (369 mL), UPC 8 50043-70646 5. 2. 1 gallon jugs, 4 per shipping case. Made by Salata Dressings, 16720 Park Row Dr., Houston, TX 77084.",
   "hazard": "This recall was initiated due to potential Salmonella contamination in diced jalape¿no received from the supplier",
   "remedy": null,
   "categories": [
    "food"
   ],
   "agency_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-1398-2026%22",
   "url": "https://consumersun.com/recall/fda-h-1398-2026-salata-dressings-llc-salata-salad-kitchen-jalapen"
  },
  {
   "agency": "FDA",
   "recall_id": "H-1409-2026",
   "date": "2026-10-07",
   "title": "TODD'S SEEDS LLC: Todd's Seeds Variety Pack of Sprouting Seeds - Broccoli recall",
   "firm": "TODD'S SEEDS LLC",
   "product": "Todd's Seeds Variety Pack of Sprouting Seeds - Broccoli, Alfalfa, Radish Mung & Clover, packaged as a multi-pack consisting of 2 oz. heat-sealed resealable bags each",
   "hazard": "Products contain alfalfa seed recalled by the supplier and may be contaminated with E. coli and/or Salmonella (downstream recall)",
   "remedy": null,
   "categories": [
    "food"
   ],
   "agency_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-1409-2026%22",
   "url": "https://consumersun.com/recall/fda-h-1409-2026-todd-s-seeds-llc-todd-s-seeds-variety-pack-of"
  },
  {
   "agency": "FDA",
   "recall_id": "H-1408-2026",
   "date": "2026-10-07",
   "title": "TODD'S SEEDS LLC: Todd's Seeds Alfalfa & Mung Bundle (1lb each) recall",
   "firm": "TODD'S SEEDS LLC",
   "product": "Todd's Seeds Alfalfa & Mung Bundle (1lb each), packaged separately in heat-sealed resealable bags",
   "hazard": "Products contain alfalfa seed recalled by the supplier and may be contaminated with E. coli and/or Salmonella (downstream recall)",
   "remedy": null,
   "categories": [
    "food"
   ],
   "agency_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-1408-2026%22",
   "url": "https://consumersun.com/recall/fda-h-1408-2026-todd-s-seeds-llc-todd-s-seeds-alfalfa-and-mung"
  },
  {
   "agency": "FDA",
   "recall_id": "H-0001-2027",
   "date": "2026-10-07",
   "title": "SLT Foods Inc.: Khazana The Treasure Spice Magic Fennel Candy recall",
   "firm": "SLT Foods Inc.",
   "product": "Khazana The Treasure Spice Magic Fennel Candy, 5 lbs., Poly Plastic Bag, 4 per case",
   "hazard": "Undeclared Yellow 5 & 6, Red 3, and Blue 1",
   "remedy": null,
   "categories": [
    "food"
   ],
   "agency_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0001-2027%22",
   "url": "https://consumersun.com/recall/fda-h-0001-2027-slt-foods-inc-khazana-the-treasure-spice-magic"
  },
  {
   "agency": "FDA",
   "recall_id": "H-1406-2026",
   "date": "2026-10-07",
   "title": "TODD'S SEEDS LLC: Todd's Seeds Sprouting Seed Mix - Broccoli recall",
   "firm": "TODD'S SEEDS LLC",
   "product": "Todd's Seeds Sprouting Seed Mix - Broccoli, Radish, Alfalfa, packaged in heat-sealed resealable bags in the following sizes: 1/4 lb., 1/2 lb., 1 lb., and 5 lb.",
   "hazard": "Products contain alfalfa seed recalled by the supplier and may be contaminated with E. coli and/or Salmonella (downstream recall)",
   "remedy": null,
   "categories": [
    "food"
   ],
   "agency_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-1406-2026%22",
   "url": "https://consumersun.com/recall/fda-h-1406-2026-todd-s-seeds-llc-todd-s-seeds-sprouting-seed-mix"
  },
  {
   "agency": "FDA",
   "recall_id": "H-1400-2026",
   "date": "2026-10-07",
   "title": "TOJI CO.: Cloud Cafe branded Collagen Milk recall",
   "firm": "TOJI CO.",
   "product": "Cloud Cafe branded Collagen Milk; Strawberry Milk Zero; Caffeine Free; 10pc/box",
   "hazard": "Undeclared allergen ingredient (fish)",
   "remedy": null,
   "categories": [
    "food"
   ],
   "agency_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-1400-2026%22",
   "url": "https://consumersun.com/recall/fda-h-1400-2026-toji-co-cloud-cafe-branded-collagen-milk"
  },
  {
   "agency": "FDA",
   "recall_id": "H-1401-2026",
   "date": "2026-10-07",
   "title": "Pacific Health Sciences Llc: Organiccs Absolutely Pure recall",
   "firm": "Pacific Health Sciences Llc",
   "product": "Organiccs Absolutely Pure, Type-1 Hydrolyzed Collagen Peptides, All-Natural Aid for Strengthening Hair, Skin, Nails, Muscles & Joints, 180 Veggie Capsules. UPC: none",
   "hazard": "Undeclared shellfish (crab shell): source of ingredient Glucosamine sulfate",
   "remedy": null,
   "categories": [
    "food"
   ],
   "agency_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-1401-2026%22",
   "url": "https://consumersun.com/recall/fda-h-1401-2026-pacific-health-sciences-llc-organiccs-absolutely"
  },
  {
   "agency": "FDA",
   "recall_id": "H-1404-2026",
   "date": "2026-10-07",
   "title": "TODD'S SEEDS LLC: Todd's Seeds Alfalfa Sprouting Seeds recall",
   "firm": "TODD'S SEEDS LLC",
   "product": "Todd's Seeds Alfalfa Sprouting Seeds, packaged in heat-sealed resealable bags in the following sizes: 1/4 lb., 1/2 lb., 1 lb., 2.5 lb., and 5 lb.",
   "hazard": "Products contain alfalfa seed recalled by the supplier and may be contaminated with E. coli and/or Salmonella (downstream recall)",
   "remedy": null,
   "categories": [
    "food"
   ],
   "agency_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-1404-2026%22",
   "url": "https://consumersun.com/recall/fda-h-1404-2026-todd-s-seeds-llc-todd-s-seeds-alfalfa-sprouting"
  },
  {
   "agency": "FDA",
   "recall_id": "D-0879-2026",
   "date": "2026-10-07",
   "title": "SV Labs Toronto Corporation: Benzoyl Peroxide Wash recall",
   "firm": "SV Labs Toronto Corporation",
   "product": "Benzoyl Peroxide Wash, USP, 10%, packaged in a)5 FL OZ (148mL) bottles (NDC 0536-1261-63), and b) 8.5 FL OZ (237 mL) bottles (NDC 0536-1351-42), Distributed by: Rugby Laboratories, 17177 N. Laurel Park Drive, Suite 233, Livonia, MI 48152.",
   "hazard": "Microbial contamination of topical product.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0879-2026%22",
   "url": "https://consumersun.com/recall/fda-d-0879-2026-sv-labs-toronto-corporation-benzoyl-peroxide-wash"
  },
  {
   "agency": "FDA",
   "recall_id": "D-0873-2026",
   "date": "2026-10-07",
   "title": "Amneal Pharmaceuticals, LLC: Estradiol Gel recall",
   "firm": "Amneal Pharmaceuticals, LLC",
   "product": "Estradiol Gel, 0.1%, 0.25 mg, 30-packets per carton, Rx only, Distributed by: Amneal Pharmaceuticals LLC, Bridgewater, NJ 08907, NDC 69238-2452-3.",
   "hazard": "Defective Container; packets were found to be either empty or partially full.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0873-2026%22",
   "url": "https://consumersun.com/recall/fda-d-0873-2026-amneal-pharmaceuticals-llc-estradiol-gel"
  },
  {
   "agency": "FDA",
   "recall_id": "D-0874-2026",
   "date": "2026-10-07",
   "title": "Aurolab Trust: FOCUS PI Hypromellose 0 recall",
   "firm": "Aurolab Trust",
   "product": "FOCUS PI Hypromellose 0.7% Formula, 0.3 FL O (10 mL) per vial, STERILE, Manufactured for: Covalent Management, Inc., Manassas, VA 20109. NDC: 82724-007-19",
   "hazard": "Lack of Assurance of Sterility",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0874-2026%22",
   "url": "https://consumersun.com/recall/fda-d-0874-2026-aurolab-trust-focus-pi-hypromellose-0"
  },
  {
   "agency": "FDA",
   "recall_id": "D-0875-2026",
   "date": "2026-10-07",
   "title": "TerSera Therapeutics LLC: Zoladex (goserelin) implant recall",
   "firm": "TerSera Therapeutics LLC",
   "product": "Zoladex (goserelin) implant, 3.6 mg, One single-Use Syringe packaged in a carton, Rx only, Manufactured for: TerSera therapeutics LLC, Deerfield, IL 60015, BY: AstraZeneca UK Limited, Macclesfield, England, Product of Switzerland, website at www.zoladex.com, NDC 70720-950-36.",
   "hazard": "Temperature Abuse: Product sat in a non-temperature-controlled FedEx trailer at ambient outdoor conditions for 25.5 hours.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0875-2026%22",
   "url": "https://consumersun.com/recall/fda-d-0875-2026-tersera-therapeutics-llc-zoladex-goserelin-implant"
  },
  {
   "agency": "FDA",
   "recall_id": "D-0877-2026",
   "date": "2026-10-07",
   "title": "Apotex Corp.: Paroxetine Extended-Release Tablets recall",
   "firm": "Apotex Corp.",
   "product": "Paroxetine Extended-Release Tablets, 37.5mg, 30-count bottle, Rx only, Manufactured by: Apotex Inc., Toronto, Ontario, Canada M9L 1T9, Manufactured for: Apotex Corp., Weston, Florida 33326, NDC 60505-1318-3",
   "hazard": "Failed dissolution specifications.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0877-2026%22",
   "url": "https://consumersun.com/recall/fda-d-0877-2026-apotex-corp-paroxetine-extended-release-tablets"
  },
  {
   "agency": "FDA",
   "recall_id": "D-0878-2026",
   "date": "2026-10-07",
   "title": "SV Labs Toronto Corporation: Benzoyl Peroxide Wash recall",
   "firm": "SV Labs Toronto Corporation",
   "product": "Benzoyl Peroxide Wash, USP, 5%, 5 FL OZ (148 mL), Distributed by: Rugby Laboratories, 17177 N. Laurel Park Drive, Suite 233, Livonia, MI 48152. NDC: 0536-1259-63",
   "hazard": "Microbial contamination of topical product.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0878-2026%22",
   "url": "https://consumersun.com/recall/fda-d-0878-2026-sv-labs-toronto-corporation-benzoyl-peroxide-wash"
  },
  {
   "agency": "FDA",
   "recall_id": "D-0876-2026",
   "date": "2026-10-07",
   "title": "Par Health USA, LLC: Buprenorphine Hydrochloride recall",
   "firm": "Par Health USA, LLC",
   "product": "Buprenorphine Hydrochloride, Injection 0.3 mg/mL, Rx Only, 5 x 1 mL Single Dose Vials, Manufactured for: Endo USA, Malvern, PA, NDC 42023-179-05",
   "hazard": "Crystallization",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0876-2026%22",
   "url": "https://consumersun.com/recall/fda-d-0876-2026-par-health-usa-llc-buprenorphine-hydrochloride"
  },
  {
   "agency": "FDA",
   "recall_id": "D-0010-2027",
   "date": "2026-10-07",
   "title": "Ajanta Pharma USA Inc: Ranolazine Extended-Release Tablets recall",
   "firm": "Ajanta Pharma USA Inc",
   "product": "Ranolazine Extended-Release Tablets, 1000 mg, 60-count bottle, Rx Only, Marketed by: Ajanta Pharma USA Inc., Bridgewater, NJ 08807. NDC: 27241-126-02",
   "hazard": "Failed Dissolution Specifications: below specification",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0010-2027%22",
   "url": "https://consumersun.com/recall/fda-d-0010-2027-ajanta-pharma-usa-inc-ranolazine-extended-release"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-0004-2027",
   "date": "2026-10-07",
   "title": "ASP Global, LLC.: Brand Name: Expressaire Product Name: DISPOSABLE TOURNIQUET CUFF recall",
   "firm": "ASP Global, LLC.",
   "product": "Brand Name: Expressaire Product Name: DISPOSABLE TOURNIQUET CUFF, 30\" X 4\" 2-LINE (CS 18) WHITE Model/Catalog Number: 553323 Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. It is non-invasive device. Tourniquet Cuffs are intended for use in surgical procedures that requires the interruption of blood flow and clear visualization of the operative field. Component: No",
   "hazard": "Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0004-2027%22",
   "url": "https://consumersun.com/recall/fda-z-0004-2027-asp-global-llc-brand-name-expressaire-product"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-3228-2026",
   "date": "2026-10-07",
   "title": "Medline Industries, LP: Medline Basic Homecare Beds and Medlite Homecare Beds and Accessories MDR107000P BED recall",
   "firm": "Medline Industries, LP",
   "product": "Medline Basic Homecare Beds and Medlite Homecare Beds and Accessories MDR107000P BED, MANUAL, MEDLITE",
   "hazard": "Potential fire hazard involving the hand control pendant and associated wiring used with affected beds. Pendant or pendant wiring may overheat, potentially leading to smoking, sparking, melting, burning, or fire. Additional products added to 11/26/2025 recall.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3228-2026%22",
   "url": "https://consumersun.com/recall/fda-z-3228-2026-medline-industries-lp-medline-basic-homecare-beds"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-3309-2026",
   "date": "2026-10-07",
   "title": "Philips North America: Ingenia 3 recall",
   "firm": "Philips North America",
   "product": "Ingenia 3.0T and 3.0T CX; Model number (REF): 1. 781342 (3.0T), 2. 781377 (3.0T), 3. 782103 (3.0T), 4. 781271 (3.0T CX); Software Versions: R11, R12 and R13;",
   "hazard": "When exporting diffusion tensor imaging (DTI) scans from a MR system using the Enhanced MR DICOM format, the exports contain incorrect data (diffusion directions). If the Enhanced MR DICOM export is used in conjunction with third-party software for tractography (e.g. for mapping nerve fiber pathways in the brain), the software will not be able to correctly process the DTI data for reconstruction.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3309-2026%22",
   "url": "https://consumersun.com/recall/fda-z-3309-2026-philips-north-america-ingenia-3"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-0022-2027",
   "date": "2026-10-07",
   "title": "ASP Global, LLC.: Brand Name: Expressaire Product Name: DISPOSABLE TOURNIQUET CUFF recall",
   "firm": "ASP Global, LLC.",
   "product": "Brand Name: Expressaire Product Name: DISPOSABLE TOURNIQUET CUFF, 8\" X 2.5\" 2-LINE (CS 12) LIGHT BLUE Model/Catalog Number: A70107001 Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. It is non-invasive device. Tourniquet Cuffs are intended for use in surgical procedures that requires the interruption of blood flow and clear visualization of the operative field. Component: No",
   "hazard": "Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0022-2027%22",
   "url": "https://consumersun.com/recall/fda-z-0022-2027-asp-global-llc-brand-name-expressaire-product"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-0037-2027",
   "date": "2026-10-07",
   "title": "ASP Global, LLC.: Brand Name: Expressaire Product Name:DISPOSABLE BB TOURNQUET CUFF recall",
   "firm": "ASP Global, LLC.",
   "product": "Brand Name: Expressaire Product Name:DISPOSABLE BB TOURNQUET CUFF, 26\" X 6\" DUAL BLADDER, 2-LINE (CS 12) ORANGE Model/Catalog Number: A70107017 Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. It is non-invasive device. Tourniquet Cuffs are intended for use in surgical procedures that requires the interruption of blood flow and clear visualization of the operative field. Component: No",
   "hazard": "Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0037-2027%22",
   "url": "https://consumersun.com/recall/fda-z-0037-2027-asp-global-llc-brand-name-expressaire-product"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-3327-2026",
   "date": "2026-10-07",
   "title": "SPECTRUM MEDICAL SRL: Brand Name: Quantum PureFlow Product Name: Quantum PureFlow Standard Heat Exchanger High F recall",
   "firm": "SPECTRUM MEDICAL SRL",
   "product": "Brand Name: Quantum PureFlow Product Name: Quantum PureFlow Standard Heat Exchanger High Flow 3/8 W Model/Catalog Number: HX55V-S0W Software Version: N/A Product Description: The Quantum PureFlow Standard Heat Exchanger is intended to be used with a compatible Heater/Cooler system to heat/cool blood during routine cardiopulmonary bypass (CPB) procedures up to 6 hours in duration with a maximum flow rate of 8 l/min. Quantum PureFlow Standard Heat Exchanger is a single use device which allows heating/cooling the blood during extracorporeal circulation. The device is sold sterile in a blister pack in a multiple box of 4 units. Device surfaces in contact with blood are treated with a phosphorylcholine-based biocompatible coating. The device has been designed to be powered by heaters coolers that use water or a glycol-based heat transfer fluid (HTF). Component: N/A",
   "hazard": "Due to blood-to-glycol leak in the heat exchanger.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3327-2026%22",
   "url": "https://consumersun.com/recall/fda-z-3327-2026-spectrum-medical-srl-brand-name-quantum-pureflow"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-3305-2026",
   "date": "2026-10-07",
   "title": "Merit Medical Systems, Inc.: Embosphere 500-700 micrometer 2 mL Syringe Sterile Steam recall",
   "firm": "Merit Medical Systems, Inc.",
   "product": "Embosphere 500-700 micrometer 2 mL Syringe Sterile Steam, REF: S420GH/EUA, S620GH/EUA; Embosphere 700-900 micrometer 2 mL Syringe Sterile Steam, REF: S820GH/CAB; Embosphere 900-1200 micrometer 2 mL Syringe Sterile Steam, REF: S1020GH/C, S1020GH/EUA",
   "hazard": "Microspheres used in embolization of tumors, prostatic arteries, arteriovenous malformations, and blood vessels may have holes in packaging that may affect the sterile barrier, which if used could lead to infection.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3305-2026%22",
   "url": "https://consumersun.com/recall/fda-z-3305-2026-merit-medical-systems-inc-embosphere-500-700"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-3277-2026",
   "date": "2026-10-07",
   "title": "Shanghai United Imaging Healthcare Co., Ltd.: Computed Tomography X-ray System recall",
   "firm": "Shanghai United Imaging Healthcare Co., Ltd.",
   "product": "Computed Tomography X-ray System, Model: uCT 530 with software",
   "hazard": "Positron emission tomography and computed tomography x-ray systems have a software problem when Split or Local function is enabled, and multiple RIS exams are merged into a single study, that prevents patient images from being visible on the Patient Administration interface, which may result in the need for rescans.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3277-2026%22",
   "url": "https://consumersun.com/recall/fda-z-3277-2026-shanghai-united-imaging-healthcare-co-ltd"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-3325-2026",
   "date": "2026-10-07",
   "title": "Percussionaire Corporation: Intrapulmonary Percussive Ventilation recall",
   "firm": "Percussionaire Corporation",
   "product": "Intrapulmonary Percussive Ventilation, IPV HC, Product Number: S00009; Phasitron, P5-HC",
   "hazard": "Labeling updated warning not to use Intrapulmonary percussive ventilation (IPV) in conjunction with volatile anesthetic delivery systems because IPV may alter controlled delivery of volatile anesthetic agents, resulting in deeper/lighter anesthetic effects that may result in hypertonia/hypotonia, tachycardia/ bradycardia, elevated intracranial pressure, awareness during anesthesia, oversedation",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3325-2026%22",
   "url": "https://consumersun.com/recall/fda-z-3325-2026-percussionaire-corporation-intrapulmonary"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-0060-2027",
   "date": "2026-10-07",
   "title": "ASP Global, LLC.: Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 44\" 2 LINE (10) Model/Catalog Numb recall",
   "firm": "ASP Global, LLC.",
   "product": "Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 44\" 2 LINE (10) Model/Catalog Number: DT-7044-02Q Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. It is non-invasive device. Tourniquet Cuffs are intended for use in surgical procedures that requires the interruption of blood flow and clear visualization of the operative field. Component: No",
   "hazard": "Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0060-2027%22",
   "url": "https://consumersun.com/recall/fda-z-0060-2027-asp-global-llc-brand-name-mpr-product-name-single"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-3313-2026",
   "date": "2026-10-07",
   "title": "Philips North America: MR 7700 recall",
   "firm": "Philips North America",
   "product": "MR 7700; Model number (REF): 1. 782120, 2. 782153, 3. 782155, 4. 782199; Software Versions: R11, R12 and R13;",
   "hazard": "When exporting diffusion tensor imaging (DTI) scans from a MR system using the Enhanced MR DICOM format, the exports contain incorrect data (diffusion directions). If the Enhanced MR DICOM export is used in conjunction with third-party software for tractography (e.g. for mapping nerve fiber pathways in the brain), the software will not be able to correctly process the DTI data for reconstruction.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3313-2026%22",
   "url": "https://consumersun.com/recall/fda-z-3313-2026-philips-north-america-mr-7700"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-0018-2027",
   "date": "2026-10-07",
   "title": "ASP Global, LLC.: Brand Name: Expressaire Product Name: DISPOSABLE TOURNIQUET CUFF recall",
   "firm": "ASP Global, LLC.",
   "product": "Brand Name: Expressaire Product Name: DISPOSABLE TOURNIQUET CUFF, 20\" X 6\" 1-LINE (CS 10) NAVY BLUE Model/Catalog Number: 564017 Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. It is non-invasive device. Tourniquet Cuffs are intended for use in surgical procedures that requires the interruption of blood flow and clear visualization of the operative field. Component: No",
   "hazard": "Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0018-2027%22",
   "url": "https://consumersun.com/recall/fda-z-0018-2027-asp-global-llc-brand-name-expressaire-product"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-3297-2026",
   "date": "2026-10-07",
   "title": "Cardinal Health 200, LLC: Presource Packs Containing Stryker StrykeFlow PS and AHTO tube sets: 1) KIT recall",
   "firm": "Cardinal Health 200, LLC",
   "product": "Presource Packs Containing Stryker StrykeFlow PS and AHTO tube sets: 1) KIT, GYN LAPAROSCOPY NEW HAN , Catalog Number: PB23GLNLAC; 2) KIT, GYN LAPAROSCOPY NEW HAN , Catalog Number: PB23GLNLA1; 3) KIT, GYN LAPAROSCOPY NEW HAN , Catalog Number: PB23GLNLA2; 4) KIT, GYN LAPAROSCOPY NEW HAN , Catalog Number: PB23GLNLA3; 5) KIT, GYN LAPAROSCOPY NEW HAN , Catalog Number: PB23GLNLA4; 6) KIT, GYN ROBOTIC NEW HAN , Catalog Number: PB23GRNLD; 7) KIT, GYN ROBOTIC NEW HAN , Catalog Number: PB23GRNLE; 8) KIT, GYN ROBOTIC NEW HAN , Catalog Number: PB23GRNL5; 9) KIT, GYN ROBOTIC NEW HAN , Catalog Number: PB23GRNL6; 10) MVHS GU GYN ROBOT PACK , Catalog Number: SOTDKGREFB",
   "hazard": "The kits contain tube sets with handpieces that may leak during use. The impacted devices can have the following failures: fluid leakage from the hand piece that can pool on the floor. The impact can range from user dissatisfaction to the potential for the user of slip and fall.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3297-2026%22",
   "url": "https://consumersun.com/recall/fda-z-3297-2026-cardinal-health-200-llc-presource-packs"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-3328-2026",
   "date": "2026-10-07",
   "title": "SPECTRUM MEDICAL SRL: Brand Name: Quantum PureFlow Product Name: Quantum PureFlow Standard Heat Exchanger High F recall",
   "firm": "SPECTRUM MEDICAL SRL",
   "product": "Brand Name: Quantum PureFlow Product Name: Quantum PureFlow Standard Heat Exchanger High Flow 3/8 Model/Catalog Number: HX55W-S0 Software Version: N/A Product Description: The Quantum PureFlow Standard Heat Exchanger is intended to be used with a compatible Heater/Cooler system to heat/cool blood during routine cardiopulmonary bypass (CPB) procedures up to 6 hours in duration with a maximum flow rate of 8 l/min. Quantum PureFlow Standard Heat Exchanger is a single use device which allows heating/cooling the blood during extracorporeal circulation. The device is sold sterile in a blister pack in a multiple box of 4 units. Device surfaces in contact with blood are treated with a phosphorylcholine-based biocompatible coating. The device has been designed to be powered by heaters coolers that use water or a glycol-based heat transfer fluid (HTF). Component: N/A",
   "hazard": "Due to blood-to-glycol leak in the heat exchanger.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3328-2026%22",
   "url": "https://consumersun.com/recall/fda-z-3328-2026-spectrum-medical-srl-brand-name-quantum-pureflow"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-0012-2027",
   "date": "2026-10-07",
   "title": "ASP Global, LLC.: Brand Name: Expressaire Product Name: DISPOSABLE TOURNIQUET CUFF recall",
   "firm": "ASP Global, LLC.",
   "product": "Brand Name: Expressaire Product Name: DISPOSABLE TOURNIQUET CUFF, 30\" X 4\" 1-LINE (CS 10) WHITE Model/Catalog Number: 564010 Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. It is non-invasive device. Tourniquet Cuffs are intended for use in surgical procedures that requires the interruption of blood flow and clear visualization of the operative field. Component: No",
   "hazard": "Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0012-2027%22",
   "url": "https://consumersun.com/recall/fda-z-0012-2027-asp-global-llc-brand-name-expressaire-product"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-0028-2027",
   "date": "2026-10-07",
   "title": "ASP Global, LLC.: Brand Name: Expressaire Product Name:DISPOSABLE TOURNIQUET CUFF recall",
   "firm": "ASP Global, LLC.",
   "product": "Brand Name: Expressaire Product Name:DISPOSABLE TOURNIQUET CUFF, 18\" X 4\" 2-LINE (CS 18) RED Model/Catalog Number: A70107007 Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. It is non-invasive device. Tourniquet Cuffs are intended for use in surgical procedures that requires the interruption of blood flow and clear visualization of the operative field. Component: No",
   "hazard": "Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0028-2027%22",
   "url": "https://consumersun.com/recall/fda-z-0028-2027-asp-global-llc-brand-name-expressaire-product"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-0038-2027",
   "date": "2026-10-07",
   "title": "ASP Global, LLC.: Brand Name: ASP Global Product Name:DISPOSABLE TOURNIQUET CUFF recall",
   "firm": "ASP Global, LLC.",
   "product": "Brand Name: ASP Global Product Name:DISPOSABLE TOURNIQUET CUFF, 12\" X 3.5\" 2-Line, Plum Model/Catalog Number: ASP-564003 Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. It is non-invasive device. Tourniquet Cuffs are intended for use in surgical procedures that requires the interruption of blood flow and clear visualization of the operative field. Component: No",
   "hazard": "Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0038-2027%22",
   "url": "https://consumersun.com/recall/fda-z-0038-2027-asp-global-llc-brand-name-asp-global-product-name"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-0003-2027",
   "date": "2026-10-07",
   "title": "ASP Global, LLC.: Brand Name: Expressaire Product Name: DISPOSABLE TOURNIQUET CUFF recall",
   "firm": "ASP Global, LLC.",
   "product": "Brand Name: Expressaire Product Name: DISPOSABLE TOURNIQUET CUFF, 30\" X 4\" 1-LINE (CS 18) WHITE Model/Catalog Number: 553322 Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. It is non-invasive device. Tourniquet Cuffs are intended for use in surgical procedures that requires the interruption of blood flow and clear visualization of the operative field. Component: No",
   "hazard": "Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0003-2027%22",
   "url": "https://consumersun.com/recall/fda-z-0003-2027-asp-global-llc-brand-name-expressaire-product"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-3294-2026",
   "date": "2026-10-07",
   "title": "American Contract Systems Inc: Medical convenience kits containing BD CliniClean Pericare Wipes within BD Urinary Cathete recall",
   "firm": "American Contract Systems Inc",
   "product": "Medical convenience kits containing BD CliniClean Pericare Wipes within BD Urinary Catheter Trays ABDOMINAL HYSTERECTOMY - 205989 Model No. MHAH55AM LAVH-LAP COLON Model No. SPLL54U VAG HYST PACK Model No. SPVH62P",
   "hazard": "Kits contain manufacturer-recalled perineal care (pericare) wipes within urinary catheter trays, which may be contaminated with a lubricant used during the manufacturing process. Use of a contaminated wipe may lead to localized skin effects such as irritation, erythema, or mild inflammation. Failure to perform pericare due to disposal of contaminated wipes may increase risk of localized infection or catheter-associated urinary tract infection (CAUTI).",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3294-2026%22",
   "url": "https://consumersun.com/recall/fda-z-3294-2026-american-contract-systems-inc-medical-convenience"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-3276-2026",
   "date": "2026-10-07",
   "title": "Volcano Corp: Philips IntraSight Plus REF: 797423 and 797417 100-120v-220-240v recall",
   "firm": "Volcano Corp",
   "product": "Philips IntraSight Plus REF: 797423 and 797417 100-120v-220-240v,50/60hZ, 1000 VA",
   "hazard": "Software system may associate image data from one patient with another patient's record, potentially resulting in incorrect diagnosis or treatment.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3276-2026%22",
   "url": "https://consumersun.com/recall/fda-z-3276-2026-volcano-corp-philips-intrasight-plus-ref-797423"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-0029-2027",
   "date": "2026-10-07",
   "title": "ASP Global, LLC.: Brand Name: Expressaire Product Name:DISPOSABLE TOURNIQUET CUFF recall",
   "firm": "ASP Global, LLC.",
   "product": "Brand Name: Expressaire Product Name:DISPOSABLE TOURNIQUET CUFF, 24\" X 4\" 1-LINE (CS 18) YELLOW Model/Catalog Number: A70107008 Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. It is non-invasive device. Tourniquet Cuffs are intended for use in surgical procedures that requires the interruption of blood flow and clear visualization of the operative field. Component: No",
   "hazard": "Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0029-2027%22",
   "url": "https://consumersun.com/recall/fda-z-0029-2027-asp-global-llc-brand-name-expressaire-product"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-0067-2027",
   "date": "2026-10-07",
   "title": "Custom Interventional Pain Management, LLC: Brand Name: Ferndale Laboratories recall",
   "firm": "Custom Interventional Pain Management, LLC",
   "product": "Brand Name: Ferndale Laboratories; Medline; Custom Interventional Pain Management CIPM Product Name: Mastisol Skin Adhesive Model/Catalog Number: 24161B (Ferndale and Medline); Tray 17025 17g continuous PBN tray (CIPM) Software Version: n/a Product Description: Skin Adhesive in a narrow plastic sterilized tube. Mastisol is a skin glue often used during surgical procedures. Continuous epidural trays are designed for use by anesthesiologists and radiologists in the administration of regional anesthesia. Component: surgical kits",
   "hazard": "Due to manufacturing issues with the liquid skin adhesive containing in surgical convenience trays/kits.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0067-2027%22",
   "url": "https://consumersun.com/recall/fda-z-0067-2027-custom-interventional-pain-management-llc-brand"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-3322-2026",
   "date": "2026-10-07",
   "title": "Percussionaire Corporation: Intrapulmonary Percussive Ventilation recall",
   "firm": "Percussionaire Corporation",
   "product": "Intrapulmonary Percussive Ventilation, IPV-2C, Product Number: S00002-C; Phasitron 5, Product Number: P5 used with Instruction Manual",
   "hazard": "Labeling updated warning not to use Intrapulmonary percussive ventilation (IPV) in conjunction with volatile anesthetic delivery systems because IPV may alter controlled delivery of volatile anesthetic agents, resulting in deeper/lighter anesthetic effects that may result in hypertonia/hypotonia, tachycardia/ bradycardia, elevated intracranial pressure, awareness during anesthesia, oversedation",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3322-2026%22",
   "url": "https://consumersun.com/recall/fda-z-3322-2026-percussionaire-corporation-intrapulmonary"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-3289-2026",
   "date": "2026-10-07",
   "title": "American Nitrile Operations Llc: Brand Name: Performance Pro Product Name: Performance Pro Model/Catalog Number: 72-RM50601 recall",
   "firm": "American Nitrile Operations Llc",
   "product": "Brand Name: Performance Pro Product Name: Performance Pro Model/Catalog Number: 72-RM50601,72-RM50602, 72-RM50603,72-RM50604 Product Description: Blue Nitrile Patient examination gloves",
   "hazard": "Gloves may exhibit defects such as tears, missing fingers, and debris. Use of defective gloves may lead to healthcare personnel and patient exposure to infectious pathogens leading to infection or cross-contamination, or exposure to chemical agents leading to irritation or systemic toxicities.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3289-2026%22",
   "url": "https://consumersun.com/recall/fda-z-3289-2026-american-nitrile-operations-llc-brand-name"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-3227-2026",
   "date": "2026-10-07",
   "title": "Medline Industries, LP: Medline Basic Homecare Beds and Medlite Homecare Beds and Accessories recall",
   "firm": "Medline Industries, LP",
   "product": "Medline Basic Homecare Beds and Medlite Homecare Beds and Accessories, Hand Pendants: MDR510094 PENDANT F/ MDR107002E MDR520094 PENDANT F/ MDR107003E MDR530094 PENDANT, W/ 9V BATTERY BACKUP, F/ 2E BED MDR540094 PENDANT, W/ 9V BATTERY BACKUP, F/ 3E BED",
   "hazard": "Potential fire hazard involving the hand control pendant and associated wiring used with affected beds. Pendant or pendant wiring may overheat, potentially leading to smoking, sparking, melting, burning, or fire. Additional products added to 11/26/2025 recall.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3227-2026%22",
   "url": "https://consumersun.com/recall/fda-z-3227-2026-medline-industries-lp-medline-basic-homecare-beds"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-3331-2026",
   "date": "2026-10-07",
   "title": "Penumbra Inc.: Brand Name: Penumbra System (RED 62 Reperfusion Catheter) Product Name: Penumbra System (R recall",
   "firm": "Penumbra Inc.",
   "product": "Brand Name: Penumbra System (RED 62 Reperfusion Catheter) Product Name: Penumbra System (RED 62 Reperfusion Catheter) Model/Catalog Number: THNDRRED62SKIT Software Version: N/A Product Description: Product common name: Percutaneous catheter A complete product description is provided in Attachment 1 (HHE-2026-002 RED62). Component: Penumbra System",
   "hazard": "Due to manufacturing issues reperfusion catheters may fracture.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3331-2026%22",
   "url": "https://consumersun.com/recall/fda-z-3331-2026-penumbra-inc-brand-name-penumbra-system-red-62"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-0035-2027",
   "date": "2026-10-07",
   "title": "ASP Global, LLC.: Brand Name: Expressaire Product Name:DISPOSABLE BB TOURNQUET CUFF recall",
   "firm": "ASP Global, LLC.",
   "product": "Brand Name: Expressaire Product Name:DISPOSABLE BB TOURNQUET CUFF, 20\" X 6\" DUAL BLADDER 1-LINE (CS 12) NAVY BLUE Model/Catalog Number: A70107014 Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. It is non-invasive device. Tourniquet Cuffs are intended for use in surgical procedures that requires the interruption of blood flow and clear visualization of the operative field. Component: No",
   "hazard": "Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0035-2027%22",
   "url": "https://consumersun.com/recall/fda-z-0035-2027-asp-global-llc-brand-name-expressaire-product"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-3308-2026",
   "date": "2026-10-07",
   "title": "Philips North America: Ingenia 1 recall",
   "firm": "Philips North America",
   "product": "Ingenia 1.5T, 1.5T CX, and 1.5T S; Model number (REF): 1. 781315 (1.5T), 2. 781341 (1.5T), 3. 781396 (1.5T), 4. 782115 (1.5T), 5. 782140 (1.5T), 6. 781262 (1.5T CX), 7. 781347 (1.5T S); Software Versions: R11, R12 and R13;",
   "hazard": "When exporting diffusion tensor imaging (DTI) scans from a MR system using the Enhanced MR DICOM format, the exports contain incorrect data (diffusion directions). If the Enhanced MR DICOM export is used in conjunction with third-party software for tractography (e.g. for mapping nerve fiber pathways in the brain), the software will not be able to correctly process the DTI data for reconstruction.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3308-2026%22",
   "url": "https://consumersun.com/recall/fda-z-3308-2026-philips-north-america-ingenia-1"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-3278-2026",
   "date": "2026-10-07",
   "title": "Shanghai United Imaging Healthcare Co., Ltd.: Computed Tomography X-ray System recall",
   "firm": "Shanghai United Imaging Healthcare Co., Ltd.",
   "product": "Computed Tomography X-ray System, Model: uCT 550 with software",
   "hazard": "Positron emission tomography and computed tomography x-ray systems have a software problem when Split or Local function is enabled, and multiple RIS exams are merged into a single study, that prevents patient images from being visible on the Patient Administration interface, which may result in the need for rescans.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3278-2026%22",
   "url": "https://consumersun.com/recall/fda-z-3278-2026-shanghai-united-imaging-healthcare-co-ltd"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-0045-2027",
   "date": "2026-10-07",
   "title": "ASP Global, LLC.: Brand Name: ASP Global Product Name:DISPOSABLE TOURNIQUET CUFF recall",
   "firm": "ASP Global, LLC.",
   "product": "Brand Name: ASP Global Product Name:DISPOSABLE TOURNIQUET CUFF, 34\" X 4\" 1-Line, Blue Model/Catalog Number: ASP-564012 Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. It is non-invasive device. Tourniquet Cuffs are intended for use in surgical procedures that requires the interruption of blood flow and clear visualization of the operative field. Component: No",
   "hazard": "Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0045-2027%22",
   "url": "https://consumersun.com/recall/fda-z-0045-2027-asp-global-llc-brand-name-asp-global-product-name"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-3284-2026",
   "date": "2026-10-07",
   "title": "Shanghai United Imaging Healthcare Co., Ltd.: Positron Emission Tomography and Computed Tomography System recall",
   "firm": "Shanghai United Imaging Healthcare Co., Ltd.",
   "product": "Positron Emission Tomography and Computed Tomography System, Model: uMI Panorama 35 with software",
   "hazard": "Positron emission tomography and computed tomography x-ray systems have a software problem when Split or Local function is enabled, and multiple RIS exams are merged into a single study, that prevents patient images from being visible on the Patient Administration interface, which may result in the need for rescans.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3284-2026%22",
   "url": "https://consumersun.com/recall/fda-z-3284-2026-shanghai-united-imaging-healthcare-co-ltd"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-3318-2026",
   "date": "2026-10-07",
   "title": "Philips North America: Evolution upgrade 1 recall",
   "firm": "Philips North America",
   "product": "Evolution upgrade 1.5T amd Evolution upgrade 3.0T; Model number (REF): 1. 782116 (1.5T), 2. 782148 (1.5T), 3. 782166 (1.5T), 4. 782201(1.5T), 5. 782117 (3.0T), 6. 782143 (3.0T), 7. 782162 (3.0T); Software Versions: R11, R12 and R13;",
   "hazard": "When exporting diffusion tensor imaging (DTI) scans from a MR system using the Enhanced MR DICOM format, the exports contain incorrect data (diffusion directions). If the Enhanced MR DICOM export is used in conjunction with third-party software for tractography (e.g. for mapping nerve fiber pathways in the brain), the software will not be able to correctly process the DTI data for reconstruction.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3318-2026%22",
   "url": "https://consumersun.com/recall/fda-z-3318-2026-philips-north-america-evolution-upgrade-1"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-3296-2026",
   "date": "2026-10-07",
   "title": "Cardinal Health 200, LLC: Presource Packs Containing Stryker StrykeFlow PS and AHTO tube sets: 1) KIT recall",
   "firm": "Cardinal Health 200, LLC",
   "product": "Presource Packs Containing Stryker StrykeFlow PS and AHTO tube sets: 1) KIT,GU DAVINCI , Catalog Number: PGVMDVBWU; 2) KIT,GU DAVINCI , Catalog Number: PGVMDVBWV; 3) KIT,GU DAVINCI , Catalog Number: PGVMDVB26; 4) KIT,GU DAVINCI , Catalog Number: PGVMDVB27; 5) KIT,GU DAVINCI , Catalog Number: PGVMDVB28; 6) KIT,GU DAVINCI , Catalog Number: PGVMDVB29; 7) COLORECTAL PACK , Catalog Number: SBA73CLKFD; 8) COLORECTAL PACK , Catalog Number: SBA73CLK26",
   "hazard": "The kits contain tube sets with handpieces that may leak during use. The impacted devices can have the following failures: fluid leakage from the hand piece that can pool on the floor. The impact can range from user dissatisfaction to the potential for the user of slip and fall.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3296-2026%22",
   "url": "https://consumersun.com/recall/fda-z-3296-2026-cardinal-health-200-llc-presource-packs"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-0009-2027",
   "date": "2026-10-07",
   "title": "ASP Global, LLC.: Brand Name: Expressaire Product Name: DISPOSABLE TOURNIQUET CUFF recall",
   "firm": "ASP Global, LLC.",
   "product": "Brand Name: Expressaire Product Name: DISPOSABLE TOURNIQUET CUFF, 18\" X 4\" 2-LINE (CS 10) RED Model/Catalog Number: 564007 Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. It is non-invasive device. Tourniquet Cuffs are intended for use in surgical procedures that requires the interruption of blood flow and clear visualization of the operative field. Component: No",
   "hazard": "Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0009-2027%22",
   "url": "https://consumersun.com/recall/fda-z-0009-2027-asp-global-llc-brand-name-expressaire-product"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-0020-2027",
   "date": "2026-10-07",
   "title": "ASP Global, LLC.: Brand Name: Expressaire Product Name: DISPOSABLE TOURNIQUET CUFF recall",
   "firm": "ASP Global, LLC.",
   "product": "Brand Name: Expressaire Product Name: DISPOSABLE TOURNIQUET CUFF, 38\" X 4\" 1-LINE (CS 10) Model/Catalog Number: 564044 Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. It is non-invasive device. Tourniquet Cuffs are intended for use in surgical procedures that requires the interruption of blood flow and clear visualization of the operative field. Component: No",
   "hazard": "Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0020-2027%22",
   "url": "https://consumersun.com/recall/fda-z-0020-2027-asp-global-llc-brand-name-expressaire-product"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-0040-2027",
   "date": "2026-10-07",
   "title": "ASP Global, LLC.: Brand Name: ASP Global Product Name:DISPOSABLE TOURNIQUET CUFF recall",
   "firm": "ASP Global, LLC.",
   "product": "Brand Name: ASP Global Product Name:DISPOSABLE TOURNIQUET CUFF, 18\" X 4\" 2-Line, Red Model/Catalog Number: ASP-564007 Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. It is non-invasive device. Tourniquet Cuffs are intended for use in surgical procedures that requires the interruption of blood flow and clear visualization of the operative field. Component: No",
   "hazard": "Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0040-2027%22",
   "url": "https://consumersun.com/recall/fda-z-0040-2027-asp-global-llc-brand-name-asp-global-product-name"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-3155-2026",
   "date": "2026-10-07",
   "title": "Philips North America Llc: Philips Medical Systems Technologies Ltd recall",
   "firm": "Philips North America Llc",
   "product": "Philips Medical Systems Technologies Ltd. Spectral CT 7500, Software V5.2.x, Product Code 728333",
   "hazard": "The Bolus tracking scan application may crash with a system error message. Bolus Tracker shots may continue to occur even if the contrast threshold is reached. This may result in the patient receiving additional radiation.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3155-2026%22",
   "url": "https://consumersun.com/recall/fda-z-3155-2026-philips-north-america-llc-philips-medical-systems"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-0033-2027",
   "date": "2026-10-07",
   "title": "ASP Global, LLC.: Brand Name: Expressaire Product Name:DISPOSABLE TOURNIQUET CUFF recall",
   "firm": "ASP Global, LLC.",
   "product": "Brand Name: Expressaire Product Name:DISPOSABLE TOURNIQUET CUFF, 44\" X 4\" 1-LINE (CS 12) GREEN Model/Catalog Number: A70107012 Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. It is non-invasive device. Tourniquet Cuffs are intended for use in surgical procedures that requires the interruption of blood flow and clear visualization of the operative field. Component: No",
   "hazard": "Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0033-2027%22",
   "url": "https://consumersun.com/recall/fda-z-0033-2027-asp-global-llc-brand-name-expressaire-product"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-3287-2026",
   "date": "2026-10-07",
   "title": "Shanghai United Imaging Healthcare Co., Ltd.: Positron Emission Tomography and Computed Tomography System recall",
   "firm": "Shanghai United Imaging Healthcare Co., Ltd.",
   "product": "Positron Emission Tomography and Computed Tomography System, Model: uMI Panvivo S with software",
   "hazard": "Positron emission tomography and computed tomography x-ray systems have a software problem when Split or Local function is enabled, and multiple RIS exams are merged into a single study, that prevents patient images from being visible on the Patient Administration interface, which may result in the need for rescans.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3287-2026%22",
   "url": "https://consumersun.com/recall/fda-z-3287-2026-shanghai-united-imaging-healthcare-co-ltd"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-3280-2026",
   "date": "2026-10-07",
   "title": "Shanghai United Imaging Healthcare Co., Ltd.: Computed Tomography X-ray System recall",
   "firm": "Shanghai United Imaging Healthcare Co., Ltd.",
   "product": "Computed Tomography X-ray System, Model: uCT 780 with software",
   "hazard": "Positron emission tomography and computed tomography x-ray systems have a software problem when Split or Local function is enabled, and multiple RIS exams are merged into a single study, that prevents patient images from being visible on the Patient Administration interface, which may result in the need for rescans.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3280-2026%22",
   "url": "https://consumersun.com/recall/fda-z-3280-2026-shanghai-united-imaging-healthcare-co-ltd"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-3281-2026",
   "date": "2026-10-07",
   "title": "Shanghai United Imaging Healthcare Co., Ltd.: Computed Tomography X-ray System recall",
   "firm": "Shanghai United Imaging Healthcare Co., Ltd.",
   "product": "Computed Tomography X-ray System, Model: uCT ATLAS with software",
   "hazard": "Positron emission tomography and computed tomography x-ray systems have a software problem when Split or Local function is enabled, and multiple RIS exams are merged into a single study, that prevents patient images from being visible on the Patient Administration interface, which may result in the need for rescans.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3281-2026%22",
   "url": "https://consumersun.com/recall/fda-z-3281-2026-shanghai-united-imaging-healthcare-co-ltd"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-3272-2026",
   "date": "2026-10-07",
   "title": "Alere San Diego, Inc.: Fisher Scientific Sure-Vue Serum/Urine hCG recall",
   "firm": "Alere San Diego, Inc.",
   "product": "Fisher Scientific Sure-Vue Serum/Urine hCG, Model/ Part: FHC-202/23900529, FHC-202/23900528; Beckman Coulter Inc's ICON 25 hCG, Model/ Part: FHC-202/43025; Henry Schein One Step+ hCG Combo test in Serum or Urine, Model/ Part: FHC-202/9004075; Alere hCG Combo Cassette (25mIU/mL) in Urine (CLIA Waived) or Serum, Model/ Part: FHC-202/92225; Pro Advantage By NDC Urine/Serum Pregnancy Cassette Device, Model/ Part: FHC-202/P080021",
   "hazard": "hCG rapid tests may detect low levels of hCG below the stated assay sensitivity, which may result in false positive result.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3272-2026%22",
   "url": "https://consumersun.com/recall/fda-z-3272-2026-alere-san-diego-inc-fisher-scientific-sure-vue"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-3252-2026",
   "date": "2026-10-07",
   "title": "Draeger, Inc.: VentStar Resus Neo recall",
   "firm": "Draeger, Inc.",
   "product": "VentStar Resus Neo. Neonatal. 25 Units per Box. Part Number: MP00310 Disposable breathing circuit for use with a resuscitation module.",
   "hazard": "Potential cracks in the hose, which could lead to leakage or the hose falling off.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3252-2026%22",
   "url": "https://consumersun.com/recall/fda-z-3252-2026-draeger-inc-ventstar-resus-neo"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-3316-2026",
   "date": "2026-10-07",
   "title": "Philips North America: Upgrade dStream recall",
   "firm": "Philips North America",
   "product": "Upgrade dStream; Model number (REF): 782127; Software Versions: R11, R12 and R13;",
   "hazard": "When exporting diffusion tensor imaging (DTI) scans from a MR system using the Enhanced MR DICOM format, the exports contain incorrect data (diffusion directions). If the Enhanced MR DICOM export is used in conjunction with third-party software for tractography (e.g. for mapping nerve fiber pathways in the brain), the software will not be able to correctly process the DTI data for reconstruction.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3316-2026%22",
   "url": "https://consumersun.com/recall/fda-z-3316-2026-philips-north-america-upgrade-dstream"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-0051-2027",
   "date": "2026-10-07",
   "title": "ASP Global, LLC.: Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 26\" DUAL BLADDER recall",
   "firm": "ASP Global, LLC.",
   "product": "Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 26\" DUAL BLADDER, 2 LINE (10) Model/Catalog Number: DB-7024-02Q Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. It is non-invasive device. Tourniquet Cuffs are intended for use in surgical procedures that requires the interruption of blood flow and clear visualization of the operative field. Component: No",
   "hazard": "Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0051-2027%22",
   "url": "https://consumersun.com/recall/fda-z-0051-2027-asp-global-llc-brand-name-mpr-product-name-single"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-0027-2027",
   "date": "2026-10-07",
   "title": "ASP Global, LLC.: Brand Name: Expressaire Product Name:DISPOSABLE TOURNIQUET CUFF recall",
   "firm": "ASP Global, LLC.",
   "product": "Brand Name: Expressaire Product Name:DISPOSABLE TOURNIQUET CUFF, 18\" X 4\" 1-LINE (CS 18) RED Model/Catalog Number: A70107006 Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. It is non-invasive device. Tourniquet Cuffs are intended for use in surgical procedures that requires the interruption of blood flow and clear visualization of the operative field. Component: No",
   "hazard": "Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0027-2027%22",
   "url": "https://consumersun.com/recall/fda-z-0027-2027-asp-global-llc-brand-name-expressaire-product"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-0052-2027",
   "date": "2026-10-07",
   "title": "ASP Global, LLC.: Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 18\" 1 LINE (10) Model/Catalog Numb recall",
   "firm": "ASP Global, LLC.",
   "product": "Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 18\" 1 LINE (10) Model/Catalog Number: DT-7018-01Q Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. It is non-invasive device. Tourniquet Cuffs are intended for use in surgical procedures that requires the interruption of blood flow and clear visualization of the operative field. Component: No",
   "hazard": "Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0052-2027%22",
   "url": "https://consumersun.com/recall/fda-z-0052-2027-asp-global-llc-brand-name-mpr-product-name-single"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-3320-2026",
   "date": "2026-10-07",
   "title": "Percussionaire Corporation: In-Line Valve recall",
   "firm": "Percussionaire Corporation",
   "product": "In-Line Valve, Product Number: P5-TEE",
   "hazard": "Labeling updated warning not to use Intrapulmonary percussive ventilation (IPV) in conjunction with volatile anesthetic delivery systems because IPV may alter controlled delivery of volatile anesthetic agents, resulting in deeper/lighter anesthetic effects that may result in hypertonia/hypotonia, tachycardia/ bradycardia, elevated intracranial pressure, awareness during anesthesia, oversedation",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3320-2026%22",
   "url": "https://consumersun.com/recall/fda-z-3320-2026-percussionaire-corporation-in-line-valve"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-0036-2027",
   "date": "2026-10-07",
   "title": "ASP Global, LLC.: Brand Name: Expressaire Product Name:DISPOSABLE BB TOURNQUET CUFF recall",
   "firm": "ASP Global, LLC.",
   "product": "Brand Name: Expressaire Product Name:DISPOSABLE BB TOURNQUET CUFF, 26\" X 6\" DUAL BLADDER, 1-LINE (CS 12) ORANGE Model/Catalog Number: A70107016 Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. It is non-invasive device. Tourniquet Cuffs are intended for use in surgical procedures that requires the interruption of blood flow and clear visualization of the operative field. Component: No",
   "hazard": "Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0036-2027%22",
   "url": "https://consumersun.com/recall/fda-z-0036-2027-asp-global-llc-brand-name-expressaire-product"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-0068-2027",
   "date": "2026-10-07",
   "title": "Illumina, Inc.: NovaSeq 6000Dx including DRAGEN Server recall",
   "firm": "Illumina, Inc.",
   "product": "NovaSeq 6000Dx including DRAGEN Server, Catalog Number: 20068232; Illumina DRAGEN Server for NextSeq 550Dx, Catalog Number: 20086130",
   "hazard": "Retrospectively reported correction for an instrument intended for targeted sequencing of DNA libraries from human genomic DNA used with in vitro diagnostic assays has a server with a security vulnerability.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0068-2027%22",
   "url": "https://consumersun.com/recall/fda-z-0068-2027-illumina-inc-novaseq-6000dx-including-dragen"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-0043-2027",
   "date": "2026-10-07",
   "title": "ASP Global, LLC.: Brand Name: ASP Global Product Name:DISPOSABLE TOURNIQUET CUFF recall",
   "firm": "ASP Global, LLC.",
   "product": "Brand Name: ASP Global Product Name:DISPOSABLE TOURNIQUET CUFF, 30\" X 4\" 1-Line, White Model/Catalog Number: ASP-564010 Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. It is non-invasive device. Tourniquet Cuffs are intended for use in surgical procedures that requires the interruption of blood flow and clear visualization of the operative field. Component: No",
   "hazard": "Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0043-2027%22",
   "url": "https://consumersun.com/recall/fda-z-0043-2027-asp-global-llc-brand-name-asp-global-product-name"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-0026-2027",
   "date": "2026-10-07",
   "title": "ASP Global, LLC.: Brand Name: Expressaire Product Name:DISPOSABLE TOURNIQUET CUFF recall",
   "firm": "ASP Global, LLC.",
   "product": "Brand Name: Expressaire Product Name:DISPOSABLE TOURNIQUET CUFF, 15\" X 4\" 2-LINE (CS 12) GRAY Model/Catalog Number: A70107005 Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. It is non-invasive device. Tourniquet Cuffs are intended for use in surgical procedures that requires the interruption of blood flow and clear visualization of the operative field. Component: No",
   "hazard": "Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0026-2027%22",
   "url": "https://consumersun.com/recall/fda-z-0026-2027-asp-global-llc-brand-name-expressaire-product"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-0062-2027",
   "date": "2026-10-07",
   "title": "ASP Global, LLC.: Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 12\" 1 LINE (10) Model/Catalog Numb recall",
   "firm": "ASP Global, LLC.",
   "product": "Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 12\" 1 LINE (10) Model/Catalog Number: DT-7112-01Q Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. It is non-invasive device. Tourniquet Cuffs are intended for use in surgical procedures that requires the interruption of blood flow and clear visualization of the operative field. Component: No",
   "hazard": "Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0062-2027%22",
   "url": "https://consumersun.com/recall/fda-z-0062-2027-asp-global-llc-brand-name-mpr-product-name-single"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-3323-2026",
   "date": "2026-10-07",
   "title": "Percussionaire Corporation: Impulsator recall",
   "firm": "Percussionaire Corporation",
   "product": "Impulsator, Product Number: S00010, Phasitron 5, Product Number: P5 used with Instruction Manual",
   "hazard": "Labeling updated warning not to use Intrapulmonary percussive ventilation (IPV) in conjunction with volatile anesthetic delivery systems because IPV may alter controlled delivery of volatile anesthetic agents, resulting in deeper/lighter anesthetic effects that may result in hypertonia/hypotonia, tachycardia/ bradycardia, elevated intracranial pressure, awareness during anesthesia, oversedation",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3323-2026%22",
   "url": "https://consumersun.com/recall/fda-z-3323-2026-percussionaire-corporation-impulsator"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-3299-2026",
   "date": "2026-10-07",
   "title": "Olympus Corporation of the Americas: Olympus M3 Gold Autoclavable Foroblique Telescope 30 recall",
   "firm": "Olympus Corporation of the Americas",
   "product": "Olympus M3 Gold Autoclavable Foroblique Telescope 30. Model Number: M3-30A.",
   "hazard": "There are identified discrepancies between the sterilization parameters listed in the Instructions for Use and the sterilization parameters listed in the Japanese package insert.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3299-2026%22",
   "url": "https://consumersun.com/recall/fda-z-3299-2026-olympus-corporation-of-the-americas-olympus-m3"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-3326-2026",
   "date": "2026-10-07",
   "title": "Micro Therapeutics, Inc.: Pipeline Flex Embolization Device with Shield Technology REF PED2-300-12 UDI-DI code: 0076 recall",
   "firm": "Micro Therapeutics, Inc.",
   "product": "Pipeline Flex Embolization Device with Shield Technology REF PED2-300-12 UDI-DI code: 00763000448806 he Pipeline Flex Embolization Device with Shield Technology consists of a permanent implant combined with a guidewire based delivery system. The Pipeline Flex Embolization Device with Shield Technology implant is a braided, multi-alloy, mesh cylinder woven from platinum/tungsten and cobalt-chromium-nickel alloy wires and indicated for the endovascular treatment of adults (22 years of age or older) with large or giant wide-necked intracranial aneurysms (IAs) in the internal carotid artery from the petrous to the superior hypophyseal segments.",
   "hazard": "Due to incorrect label/product dimensions. Product is supposed to be 3.00 mm in diameter, but unit is packaging was a 2.50 mm in diameter.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3326-2026%22",
   "url": "https://consumersun.com/recall/fda-z-3326-2026-micro-therapeutics-inc-pipeline-flex-embolization"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-0050-2027",
   "date": "2026-10-07",
   "title": "ASP Global, LLC.: Brand Name: MPR Product Name:DISPOSABLE TOURNIQUET CUFF 20\" DUAL BLADDER recall",
   "firm": "ASP Global, LLC.",
   "product": "Brand Name: MPR Product Name:DISPOSABLE TOURNIQUET CUFF 20\" DUAL BLADDER, 2 LINE (10) Model/Catalog Number: DB-7020-02Q Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. It is non-invasive device. Tourniquet Cuffs are intended for use in surgical procedures that requires the interruption of blood flow and clear visualization of the operative field. Component: No",
   "hazard": "Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0050-2027%22",
   "url": "https://consumersun.com/recall/fda-z-0050-2027-asp-global-llc-brand-name-mpr-product-name"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-0017-2027",
   "date": "2026-10-07",
   "title": "ASP Global, LLC.: Brand Name: Expressaire Product Name: DISPOSABLE TOURNIQUET CUFF recall",
   "firm": "ASP Global, LLC.",
   "product": "Brand Name: Expressaire Product Name: DISPOSABLE TOURNIQUET CUFF, 44\" X 4\" 2-LINE (CS 10) GREEN Model/Catalog Number: 564015 Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. It is non-invasive device. Tourniquet Cuffs are intended for use in surgical procedures that requires the interruption of blood flow and clear visualization of the operative field. Component: No",
   "hazard": "Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0017-2027%22",
   "url": "https://consumersun.com/recall/fda-z-0017-2027-asp-global-llc-brand-name-expressaire-product"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-0057-2027",
   "date": "2026-10-07",
   "title": "ASP Global, LLC.: Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 34\" 1 LINE (10) Model/Catalog Numb recall",
   "firm": "ASP Global, LLC.",
   "product": "Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 34\" 1 LINE (10) Model/Catalog Number: DT-7034-01Q Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. It is non-invasive device. Tourniquet Cuffs are intended for use in surgical procedures that requires the interruption of blood flow and clear visualization of the operative field. Component: No",
   "hazard": "Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0057-2027%22",
   "url": "https://consumersun.com/recall/fda-z-0057-2027-asp-global-llc-brand-name-mpr-product-name-single"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-3275-2026",
   "date": "2026-10-07",
   "title": "Bard Peripheral Vascular Inc: EnCor EnCompass Breast Biopsy and Tissue Removal System Console (model number: ENCPCONSOLE recall",
   "firm": "Bard Peripheral Vascular Inc",
   "product": "EnCor EnCompass Breast Biopsy and Tissue Removal System Console (model number: ENCPCONSOLE) and Driver (model number: ENCPDRIVER) with software",
   "hazard": "Breast biopsy and tissue removal system may experience the following errors: 1) Probe calibration and /or handheld driver failure (code HH01-00020009) , 2) Pressure sensor (code E01-0054000E), which prompts the user to restart and re-calibrate; errors may lead to interruption or prolongation of the biopsy procedure, or the need for additional tissue sampling or repeat biopsy.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3275-2026%22",
   "url": "https://consumersun.com/recall/fda-z-3275-2026-bard-peripheral-vascular-inc-encor-encompass"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-0049-2027",
   "date": "2026-10-07",
   "title": "ASP Global, LLC.: Brand Name: MPR Product Name:DISPOSABLE TOURNIQUET CUFF 20\" DUAL BLADDER recall",
   "firm": "ASP Global, LLC.",
   "product": "Brand Name: MPR Product Name:DISPOSABLE TOURNIQUET CUFF 20\" DUAL BLADDER, 1 LINE (10) Model/Catalog Number: DB-7018-01Q Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. It is non-invasive device. Tourniquet Cuffs are intended for use in surgical procedures that requires the interruption of blood flow and clear visualization of the operative field. Component: No",
   "hazard": "Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0049-2027%22",
   "url": "https://consumersun.com/recall/fda-z-0049-2027-asp-global-llc-brand-name-mpr-product-name"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-3293-2026",
   "date": "2026-10-07",
   "title": "American Contract Systems Inc: Medical convenience kits containing BD CliniClean Pericare Wipes within BD Urinary Cathete recall",
   "firm": "American Contract Systems Inc",
   "product": "Medical convenience kits containing BD CliniClean Pericare Wipes within BD Urinary Catheter Trays CARDIAC HEART BUNDLE NS Model No. LMCH99P OPEN HEART 2 RCH¿ 0248495 Model No. RCOH62C",
   "hazard": "Kits contain manufacturer-recalled perineal care (pericare) wipes within urinary catheter trays, which may be contaminated with a lubricant used during the manufacturing process. Use of a contaminated wipe may lead to localized skin effects such as irritation, erythema, or mild inflammation. Failure to perform pericare due to disposal of contaminated wipes may increase risk of localized infection or catheter-associated urinary tract infection (CAUTI).",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3293-2026%22",
   "url": "https://consumersun.com/recall/fda-z-3293-2026-american-contract-systems-inc-medical-convenience"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-0016-2027",
   "date": "2026-10-07",
   "title": "ASP Global, LLC.: Brand Name: Expressaire Product Name: DISPOSABLE TOURNIQUET CUFF recall",
   "firm": "ASP Global, LLC.",
   "product": "Brand Name: Expressaire Product Name: DISPOSABLE TOURNIQUET CUFF, 44\" X 4\" 1-LINE (CS 10) GREEN Model/Catalog Number: 564014 Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. It is non-invasive device. Tourniquet Cuffs are intended for use in surgical procedures that requires the interruption of blood flow and clear visualization of the operative field. Component: No",
   "hazard": "Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0016-2027%22",
   "url": "https://consumersun.com/recall/fda-z-0016-2027-asp-global-llc-brand-name-expressaire-product"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-0053-2027",
   "date": "2026-10-07",
   "title": "ASP Global, LLC.: Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 24\" 1 LINE (10) Model/Catalog Numb recall",
   "firm": "ASP Global, LLC.",
   "product": "Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 24\" 1 LINE (10) Model/Catalog Number: DT-7024-01Q Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. It is non-invasive device. Tourniquet Cuffs are intended for use in surgical procedures that requires the interruption of blood flow and clear visualization of the operative field. Component: No",
   "hazard": "Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0053-2027%22",
   "url": "https://consumersun.com/recall/fda-z-0053-2027-asp-global-llc-brand-name-mpr-product-name-single"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-3312-2026",
   "date": "2026-10-07",
   "title": "Philips North America: MR 5300 recall",
   "firm": "Philips North America",
   "product": "MR 5300; Model number (REF): 1. 782110, 2. 782152, 3. 782156, 4. 782196; Software Versions: R11, R12 and R13;",
   "hazard": "When exporting diffusion tensor imaging (DTI) scans from a MR system using the Enhanced MR DICOM format, the exports contain incorrect data (diffusion directions). If the Enhanced MR DICOM export is used in conjunction with third-party software for tractography (e.g. for mapping nerve fiber pathways in the brain), the software will not be able to correctly process the DTI data for reconstruction.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3312-2026%22",
   "url": "https://consumersun.com/recall/fda-z-3312-2026-philips-north-america-mr-5300"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-3315-2026",
   "date": "2026-10-07",
   "title": "Philips North America: SmartPath to MR 7700 recall",
   "firm": "Philips North America",
   "product": "SmartPath to MR 7700; Model number (REF): 1. 782178, 2. 782207; Software Versions: R11, R12 and R13;",
   "hazard": "When exporting diffusion tensor imaging (DTI) scans from a MR system using the Enhanced MR DICOM format, the exports contain incorrect data (diffusion directions). If the Enhanced MR DICOM export is used in conjunction with third-party software for tractography (e.g. for mapping nerve fiber pathways in the brain), the software will not be able to correctly process the DTI data for reconstruction.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3315-2026%22",
   "url": "https://consumersun.com/recall/fda-z-3315-2026-philips-north-america-smartpath-to-mr-7700"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-3274-2026",
   "date": "2026-10-07",
   "title": "Alere San Diego, Inc.: Fisher Scientific Sure-Vue Urine hCG recall",
   "firm": "Alere San Diego, Inc.",
   "product": "Fisher Scientific Sure-Vue Urine hCG, Model/ Part: FHC-102/23900526; Henry Schein, Inc. One Step + Urine Cassette Test, Model/ Part: FHC-102/9004074, FHC-102/9004073; Alere hCG Cassette (25mIU/mL) in Urine, Model/ Part: FHC-102/92217; Cardinal Health hCG Cassette Rapid test CLIA Waived, Model/ Part: FHC-102/B1077-22; Medline HCG Pregnancy Test Cassette, Model/ Part: FHC-102/MPH12025HCG; Pro Advantage By NDC Urine Pregnancy Cassette Device, Model/ Part: FHC-102/P080063;",
   "hazard": "hCG rapid tests may detect low levels of hCG below the stated assay sensitivity, which may result in false positive result.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3274-2026%22",
   "url": "https://consumersun.com/recall/fda-z-3274-2026-alere-san-diego-inc-fisher-scientific-sure-vue"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-0015-2027",
   "date": "2026-10-07",
   "title": "ASP Global, LLC.: Brand Name: Expressaire Product Name: DISPOSABLE TOURNIQUET CUFF recall",
   "firm": "ASP Global, LLC.",
   "product": "Brand Name: Expressaire Product Name: DISPOSABLE TOURNIQUET CUFF, 34\" X 4\" 2-LINE (CS 10) BLUE Model/Catalog Number: 564013 Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. It is non-invasive device. Tourniquet Cuffs are intended for use in surgical procedures that requires the interruption of blood flow and clear visualization of the operative field. Component: No",
   "hazard": "Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0015-2027%22",
   "url": "https://consumersun.com/recall/fda-z-0015-2027-asp-global-llc-brand-name-expressaire-product"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-3303-2026",
   "date": "2026-10-07",
   "title": "Heraeus Medical GmbH (Dental Division): PALACOS MV+G pro 40 recall",
   "firm": "Heraeus Medical GmbH (Dental Division)",
   "product": "PALACOS MV+G pro 40; PALACOS MV+G pro 80. Model/Catalog Number: 5081290; 5081291. Radiopaque, poly(methyl methacrylate)-based (PMMA) bone cement, pre-filled into a mixing and application system, suitable for use with or without vacuum (ready to mix). Component: N/A",
   "hazard": "Potential for monomer liquid leakage.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3303-2026%22",
   "url": "https://consumersun.com/recall/fda-z-3303-2026-heraeus-medical-gmbh-dental-division-palacos-mv-g"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-3282-2026",
   "date": "2026-10-07",
   "title": "Shanghai United Imaging Healthcare Co., Ltd.: Computed Tomography X-ray System recall",
   "firm": "Shanghai United Imaging Healthcare Co., Ltd.",
   "product": "Computed Tomography X-ray System, Model: uCT ATLAS Astound with software",
   "hazard": "Positron emission tomography and computed tomography x-ray systems have a software problem when Split or Local function is enabled, and multiple RIS exams are merged into a single study, that prevents patient images from being visible on the Patient Administration interface, which may result in the need for rescans.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3282-2026%22",
   "url": "https://consumersun.com/recall/fda-z-3282-2026-shanghai-united-imaging-healthcare-co-ltd"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-3307-2026",
   "date": "2026-10-07",
   "title": "Philips North America: Ingenia Blue Seal SE and Blue Seal XE recall",
   "firm": "Philips North America",
   "product": "Ingenia Blue Seal SE and Blue Seal XE; Model number (REF): 1. 782185 (SE), 2. 782192 (XE); Software Versions: R11, R12 and R13;",
   "hazard": "When exporting diffusion tensor imaging (DTI) scans from a MR system using the Enhanced MR DICOM format, the exports contain incorrect data (diffusion directions). If the Enhanced MR DICOM export is used in conjunction with third-party software for tractography (e.g. for mapping nerve fiber pathways in the brain), the software will not be able to correctly process the DTI data for reconstruction.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3307-2026%22",
   "url": "https://consumersun.com/recall/fda-z-3307-2026-philips-north-america-ingenia-blue-seal-se-and"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-0007-2027",
   "date": "2026-10-07",
   "title": "ASP Global, LLC.: Brand Name: Expressaire Product Name: DISPOSABLE TOURNIQUET CUFF recall",
   "firm": "ASP Global, LLC.",
   "product": "Brand Name: Expressaire Product Name: DISPOSABLE TOURNIQUET CUFF, 15\" X 4\" 2-LINE (CS 10) GRAY Model/Catalog Number: 564005 Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. It is non-invasive device. Tourniquet Cuffs are intended for use in surgical procedures that requires the interruption of blood flow and clear visualization of the operative field. Component: No",
   "hazard": "Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0007-2027%22",
   "url": "https://consumersun.com/recall/fda-z-0007-2027-asp-global-llc-brand-name-expressaire-product"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-0025-2027",
   "date": "2026-10-07",
   "title": "ASP Global, LLC.: Brand Name: Expressaire Product Name: DISPOSABLE TOURNIQUET CUFF recall",
   "firm": "ASP Global, LLC.",
   "product": "Brand Name: Expressaire Product Name: DISPOSABLE TOURNIQUET CUFF, 15\" X 4\" 1-LINE (CS 12) GRAY Model/Catalog Number: A70107004 Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. It is non-invasive device. Tourniquet Cuffs are intended for use in surgical procedures that requires the interruption of blood flow and clear visualization of the operative field. Component: No",
   "hazard": "Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0025-2027%22",
   "url": "https://consumersun.com/recall/fda-z-0025-2027-asp-global-llc-brand-name-expressaire-product"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-0006-2027",
   "date": "2026-10-07",
   "title": "ASP Global, LLC.: Brand Name: Expressaire Product Name: DISPOSABLE TOURNIQUET CUFF recall",
   "firm": "ASP Global, LLC.",
   "product": "Brand Name: Expressaire Product Name: DISPOSABLE TOURNIQUET CUFF, 12\" X 3.5\" 2-LINE (CS 10) PLUM Model/Catalog Number: 564003 Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. It is non-invasive device. Tourniquet Cuffs are intended for use in surgical procedures that requires the interruption of blood flow and clear visualization of the operative field. Component: No",
   "hazard": "Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0006-2027%22",
   "url": "https://consumersun.com/recall/fda-z-0006-2027-asp-global-llc-brand-name-expressaire-product"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-3310-2026",
   "date": "2026-10-07",
   "title": "Philips North America: Ingenia Ambition S and Ingenia Ambition X recall",
   "firm": "Philips North America",
   "product": "Ingenia Ambition S and Ingenia Ambition X.; Model number (REF): 1. 781359 (S), 2. 782108 (S), 3. 782139 (S), 4. 782159 (S), 5. 782194 (S), 6. 781356 (X), 7. 782109 (X), 8. 782138 (X), 9. 782160 (X), 10. 782195 (X); Software Versions: R11, R12 and R13;",
   "hazard": "When exporting diffusion tensor imaging (DTI) scans from a MR system using the Enhanced MR DICOM format, the exports contain incorrect data (diffusion directions). If the Enhanced MR DICOM export is used in conjunction with third-party software for tractography (e.g. for mapping nerve fiber pathways in the brain), the software will not be able to correctly process the DTI data for reconstruction.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3310-2026%22",
   "url": "https://consumersun.com/recall/fda-z-3310-2026-philips-north-america-ingenia-ambition-s-and"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-0021-2027",
   "date": "2026-10-07",
   "title": "ASP Global, LLC.: Brand Name: Expressaire Product Name: DISPOSABLE TOURNIQUET CUFF recall",
   "firm": "ASP Global, LLC.",
   "product": "Brand Name: Expressaire Product Name: DISPOSABLE TOURNIQUET CUFF, 8\" X 2.5\" 1-LINE (CS 12) LIGHT BLUE Model/Catalog Number: A70107000 Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. It is non-invasive device. Tourniquet Cuffs are intended for use in surgical procedures that requires the interruption of blood flow and clear visualization of the operative field. Component: No",
   "hazard": "Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0021-2027%22",
   "url": "https://consumersun.com/recall/fda-z-0021-2027-asp-global-llc-brand-name-expressaire-product"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-0039-2027",
   "date": "2026-10-07",
   "title": "ASP Global, LLC.: Brand Name: ASP Global Product Name:DISPOSABLE TOURNIQUET CUFF recall",
   "firm": "ASP Global, LLC.",
   "product": "Brand Name: ASP Global Product Name:DISPOSABLE TOURNIQUET CUFF, 18\" X 4\" 1-Line, Red Model/Catalog Number: ASP-564006 Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. It is non-invasive device. Tourniquet Cuffs are intended for use in surgical procedures that requires the interruption of blood flow and clear visualization of the operative field. Component: No",
   "hazard": "Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0039-2027%22",
   "url": "https://consumersun.com/recall/fda-z-0039-2027-asp-global-llc-brand-name-asp-global-product-name"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-3298-2026",
   "date": "2026-10-07",
   "title": "Cardinal Health 200, LLC: Presource Packs Containing Stryker StrykeFlow PS and AHTO tube sets: 1) KIT recall",
   "firm": "Cardinal Health 200, LLC",
   "product": "Presource Packs Containing Stryker StrykeFlow PS and AHTO tube sets: 1) KIT, LAVH , Catalog Number: PB63VHSTC",
   "hazard": "The kits contain tube sets with handpieces that may leak during use. The impacted devices can have the following failures: fluid leakage from the hand piece that can pool on the floor. The impact can range from user dissatisfaction to the potential for the user of slip and fall.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3298-2026%22",
   "url": "https://consumersun.com/recall/fda-z-3298-2026-cardinal-health-200-llc-presource-packs"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-0044-2027",
   "date": "2026-10-07",
   "title": "ASP Global, LLC.: Brand Name: ASP Global Product Name:DISPOSABLE TOURNIQUET CUFF recall",
   "firm": "ASP Global, LLC.",
   "product": "Brand Name: ASP Global Product Name:DISPOSABLE TOURNIQUET CUFF, 30\" X 4\" 2-Line, White Model/Catalog Number: ASP-564011 Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. It is non-invasive device. Tourniquet Cuffs are intended for use in surgical procedures that requires the interruption of blood flow and clear visualization of the operative field. Component: No",
   "hazard": "Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0044-2027%22",
   "url": "https://consumersun.com/recall/fda-z-0044-2027-asp-global-llc-brand-name-asp-global-product-name"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-3286-2026",
   "date": "2026-10-07",
   "title": "Shanghai United Imaging Healthcare Co., Ltd.: Positron Emission Tomography and Computed Tomography System recall",
   "firm": "Shanghai United Imaging Healthcare Co., Ltd.",
   "product": "Positron Emission Tomography and Computed Tomography System, Model: uMI Panvivo with software",
   "hazard": "Positron emission tomography and computed tomography x-ray systems have a software problem when Split or Local function is enabled, and multiple RIS exams are merged into a single study, that prevents patient images from being visible on the Patient Administration interface, which may result in the need for rescans.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3286-2026%22",
   "url": "https://consumersun.com/recall/fda-z-3286-2026-shanghai-united-imaging-healthcare-co-ltd"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-3334-2026",
   "date": "2026-10-07",
   "title": "Wright Medical Technology, Inc.: CHARLOTTE CLAW Screw recall",
   "firm": "Wright Medical Technology, Inc.",
   "product": "CHARLOTTE CLAW Screw, REF: 40122716, intended for use with CLAW II Polyaxial Compression Plating System",
   "hazard": "Screws, intended for use with polyaxial compression plating system intended for foot osteotomies, was manufactured with missing threads on the screwheads, which if used would prevent a secure rigid engagement with the plate's internal threads, which may lead to surgery prolongation to retrieve another device, or alternative surgery method if no replacement device is readily available.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3334-2026%22",
   "url": "https://consumersun.com/recall/fda-z-3334-2026-wright-medical-technology-inc-charlotte-claw-screw"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-0065-2027",
   "date": "2026-10-07",
   "title": "ASP Global, LLC.: Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 15\" 2 LINE (10) Model/Catalog Numb recall",
   "firm": "ASP Global, LLC.",
   "product": "Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 15\" 2 LINE (10) Model/Catalog Number: DT-7115-02Q Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. It is non-invasive device. Tourniquet Cuffs are intended for use in surgical procedures that requires the interruption of blood flow and clear visualization of the operative field. Component: No",
   "hazard": "Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0065-2027%22",
   "url": "https://consumersun.com/recall/fda-z-0065-2027-asp-global-llc-brand-name-mpr-product-name-single"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-0059-2027",
   "date": "2026-10-07",
   "title": "ASP Global, LLC.: Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 44\" 1 LINE (10) Model/Catalog Numb recall",
   "firm": "ASP Global, LLC.",
   "product": "Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 44\" 1 LINE (10) Model/Catalog Number: DT-7044-01Q Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. It is non-invasive device. Tourniquet Cuffs are intended for use in surgical procedures that requires the interruption of blood flow and clear visualization of the operative field. Component: No",
   "hazard": "Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0059-2027%22",
   "url": "https://consumersun.com/recall/fda-z-0059-2027-asp-global-llc-brand-name-mpr-product-name-single"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-3329-2026",
   "date": "2026-10-07",
   "title": "Olympus Corporation of the Americas: Olympus Tripp-Lite P580-025 25ft DisplayPort Cable recall",
   "firm": "Olympus Corporation of the Americas",
   "product": "Olympus Tripp-Lite P580-025 25ft DisplayPort Cable, Model Number P580-025, an accessory used in conjunction wtih OLYSENSE Hub System",
   "hazard": "While in the high-power operating mode, a video dropout/blackout may occur when using a particular accessory cable.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3329-2026%22",
   "url": "https://consumersun.com/recall/fda-z-3329-2026-olympus-corporation-of-the-americas-olympus-tripp"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-3285-2026",
   "date": "2026-10-07",
   "title": "Shanghai United Imaging Healthcare Co., Ltd.: Positron Emission Tomography and Computed Tomography System recall",
   "firm": "Shanghai United Imaging Healthcare Co., Ltd.",
   "product": "Positron Emission Tomography and Computed Tomography System, Model: uMI Panorama GS with software",
   "hazard": "Positron emission tomography and computed tomography x-ray systems have a software problem when Split or Local function is enabled, and multiple RIS exams are merged into a single study, that prevents patient images from being visible on the Patient Administration interface, which may result in the need for rescans.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3285-2026%22",
   "url": "https://consumersun.com/recall/fda-z-3285-2026-shanghai-united-imaging-healthcare-co-ltd"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-3279-2026",
   "date": "2026-10-07",
   "title": "Shanghai United Imaging Healthcare Co., Ltd.: Computed Tomography X-ray System recall",
   "firm": "Shanghai United Imaging Healthcare Co., Ltd.",
   "product": "Computed Tomography X-ray System, Model: uCT 760 with software",
   "hazard": "Positron emission tomography and computed tomography x-ray systems have a software problem when Split or Local function is enabled, and multiple RIS exams are merged into a single study, that prevents patient images from being visible on the Patient Administration interface, which may result in the need for rescans.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3279-2026%22",
   "url": "https://consumersun.com/recall/fda-z-3279-2026-shanghai-united-imaging-healthcare-co-ltd"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-0005-2027",
   "date": "2026-10-07",
   "title": "ASP Global, LLC.: Brand Name: Expressaire Product Name: DISPOSABLE TOURNIQUET CUFF recall",
   "firm": "ASP Global, LLC.",
   "product": "Brand Name: Expressaire Product Name: DISPOSABLE TOURNIQUET CUFF, 8\" X 2.5\" 2-LINE (CS 10) Model/Catalog Number: 564001 Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. It is non-invasive device. Tourniquet Cuffs are intended for use in surgical procedures that requires the interruption of blood flow and clear visualization of the operative field. Component: No",
   "hazard": "Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0005-2027%22",
   "url": "https://consumersun.com/recall/fda-z-0005-2027-asp-global-llc-brand-name-expressaire-product"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-3311-2026",
   "date": "2026-10-07",
   "title": "Philips North America: Ingenia Elition S and Ingenia Elition X recall",
   "firm": "Philips North America",
   "product": "Ingenia Elition S and Ingenia Elition X.; Model number (REF): 1. 781357 (S), 2. 782106 (S), 3. 782137 (S), 4. 782157 (S), 5. 781358 (X), 6. 782107 (X), 7. 782119 (X), 8. 782136 (X), 9. 782158 (X), 10. 782198 (X); Software Versions: R11, R12 and R13;",
   "hazard": "When exporting diffusion tensor imaging (DTI) scans from a MR system using the Enhanced MR DICOM format, the exports contain incorrect data (diffusion directions). If the Enhanced MR DICOM export is used in conjunction with third-party software for tractography (e.g. for mapping nerve fiber pathways in the brain), the software will not be able to correctly process the DTI data for reconstruction.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3311-2026%22",
   "url": "https://consumersun.com/recall/fda-z-3311-2026-philips-north-america-ingenia-elition-s-and"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-0056-2027",
   "date": "2026-10-07",
   "title": "ASP Global, LLC.: Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 30\" 2 LINE (10) Model/Catalog Numb recall",
   "firm": "ASP Global, LLC.",
   "product": "Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 30\" 2 LINE (10) Model/Catalog Number: DT-7030-02Q Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. It is non-invasive device. Tourniquet Cuffs are intended for use in surgical procedures that requires the interruption of blood flow and clear visualization of the operative field. Component: No",
   "hazard": "Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0056-2027%22",
   "url": "https://consumersun.com/recall/fda-z-0056-2027-asp-global-llc-brand-name-mpr-product-name-single"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-0014-2027",
   "date": "2026-10-07",
   "title": "ASP Global, LLC.: Brand Name: Expressaire Product Name: DISPOSABLE TOURNIQUET CUFF recall",
   "firm": "ASP Global, LLC.",
   "product": "Brand Name: Expressaire Product Name: DISPOSABLE TOURNIQUET CUFF, 34\" X 4\" 1-LINE (CS 10) BLUE Model/Catalog Number: 564012 Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. It is non-invasive device. Tourniquet Cuffs are intended for use in surgical procedures that requires the interruption of blood flow and clear visualization of the operative field. Component: No",
   "hazard": "Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0014-2027%22",
   "url": "https://consumersun.com/recall/fda-z-0014-2027-asp-global-llc-brand-name-expressaire-product"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-0013-2027",
   "date": "2026-10-07",
   "title": "ASP Global, LLC.: Brand Name: Expressaire Product Name: DISPOSABLE TOURNIQUET CUFF recall",
   "firm": "ASP Global, LLC.",
   "product": "Brand Name: Expressaire Product Name: DISPOSABLE TOURNIQUET CUFF, 30\" X 4\" 2-LINE (CS 10) WHITE Model/Catalog Number: 564011 Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. It is non-invasive device. Tourniquet Cuffs are intended for use in surgical procedures that requires the interruption of blood flow and clear visualization of the operative field. Component: No",
   "hazard": "Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0013-2027%22",
   "url": "https://consumersun.com/recall/fda-z-0013-2027-asp-global-llc-brand-name-expressaire-product"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-0019-2027",
   "date": "2026-10-07",
   "title": "ASP Global, LLC.: Brand Name: Expressaire Product Name: DISPOSABLE TOURNIQUET CUFF recall",
   "firm": "ASP Global, LLC.",
   "product": "Brand Name: Expressaire Product Name: DISPOSABLE TOURNIQUET CUFF, 26\" X 6\" 1-LINE (CS 10) ORANGE Model/Catalog Number: 564019 Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. It is non-invasive device. Tourniquet Cuffs are intended for use in surgical procedures that requires the interruption of blood flow and clear visualization of the operative field. Component: No",
   "hazard": "Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0019-2027%22",
   "url": "https://consumersun.com/recall/fda-z-0019-2027-asp-global-llc-brand-name-expressaire-product"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-3300-2026",
   "date": "2026-10-07",
   "title": "Olympus Corporation of the Americas: Olympus M3 Gold Autoclavable Lateral Telescope 70 recall",
   "firm": "Olympus Corporation of the Americas",
   "product": "Olympus M3 Gold Autoclavable Lateral Telescope 70. Model Number: M3-70A.",
   "hazard": "There are identified discrepancies between the sterilization parameters listed in the Instructions for Use and the sterilization parameters listed in the Japanese package insert.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3300-2026%22",
   "url": "https://consumersun.com/recall/fda-z-3300-2026-olympus-corporation-of-the-americas-olympus-m3"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-3290-2026",
   "date": "2026-10-07",
   "title": "American Nitrile Operations Llc: Brand Name: Opportunity Flex Product Name: Opportunity Flex Model/Catalog Number: 72-50900 recall",
   "firm": "American Nitrile Operations Llc",
   "product": "Brand Name: Opportunity Flex Product Name: Opportunity Flex Model/Catalog Number: 72-50900, 72-50901, 72-50902, 72-50903, 72-50904 Product Description: Blue Nitrile Patient examination gloves",
   "hazard": "Gloves may exhibit defects such as tears, missing fingers, and debris. Use of defective gloves may lead to healthcare personnel and patient exposure to infectious pathogens leading to infection or cross-contamination, or exposure to chemical agents leading to irritation or systemic toxicities.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3290-2026%22",
   "url": "https://consumersun.com/recall/fda-z-3290-2026-american-nitrile-operations-llc-brand-name"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-0063-2027",
   "date": "2026-10-07",
   "title": "ASP Global, LLC.: Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 12\" 2 LINE (10) Model/Catalog Numb recall",
   "firm": "ASP Global, LLC.",
   "product": "Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 12\" 2 LINE (10) Model/Catalog Number: DT-7112-02Q Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. It is non-invasive device. Tourniquet Cuffs are intended for use in surgical procedures that requires the interruption of blood flow and clear visualization of the operative field. Component: No",
   "hazard": "Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0063-2027%22",
   "url": "https://consumersun.com/recall/fda-z-0063-2027-asp-global-llc-brand-name-mpr-product-name-single"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-0055-2027",
   "date": "2026-10-07",
   "title": "ASP Global, LLC.: Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 30\" 1 LINE (10) Model/Catalog Numb recall",
   "firm": "ASP Global, LLC.",
   "product": "Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 30\" 1 LINE (10) Model/Catalog Number: DT-7030-01Q Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. It is non-invasive device. Tourniquet Cuffs are intended for use in surgical procedures that requires the interruption of blood flow and clear visualization of the operative field. Component: No",
   "hazard": "Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0055-2027%22",
   "url": "https://consumersun.com/recall/fda-z-0055-2027-asp-global-llc-brand-name-mpr-product-name-single"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-0046-2027",
   "date": "2026-10-07",
   "title": "ASP Global, LLC.: Brand Name: ASP Global Product Name:DISPOSABLE TOURNIQUET CUFF recall",
   "firm": "ASP Global, LLC.",
   "product": "Brand Name: ASP Global Product Name:DISPOSABLE TOURNIQUET CUFF, 34\" X 4\" 2-Line, Blue Model/Catalog Number: ASP-564013 Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. It is non-invasive device. Tourniquet Cuffs are intended for use in surgical procedures that requires the interruption of blood flow and clear visualization of the operative field. Component: No",
   "hazard": "Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0046-2027%22",
   "url": "https://consumersun.com/recall/fda-z-0046-2027-asp-global-llc-brand-name-asp-global-product-name"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-3332-2026",
   "date": "2026-10-07",
   "title": "Beckman Coulter Mishima K.K.: Systems/units containing affected software/SQL BECKMAN COULTER CHEMISTRY ANALYZER AU480 RE recall",
   "firm": "Beckman Coulter Mishima K.K.",
   "product": "Systems/units containing affected software/SQL BECKMAN COULTER CHEMISTRY ANALYZER AU480 REF / UDI-DI code: B96692 / 14987666542965 B96693 / 14987666542972 B12183 / 14987666540671 The AU480 Chemistry Analyzer measure analytes in samples, in combination with appropriate reagents, calibrators, quality control (QC) material, and other accessories. This system is for in vitro diagnostic use only.",
   "hazard": "Certain AU480 chemistry analyzers, with Windows 10 IoT Enterprise 2021 LTSC PCs, may output the message System Stopped By Fatal Error: DBConnectionError AlarmDB when launching the instrument software, using PC pre-installed with Microsoft SQL Server 2022 Express. When this occurs, AlarmDB becomes unreadable and the instrument software cannot be started. This causes a delay in obtaining patient results.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3332-2026%22",
   "url": "https://consumersun.com/recall/fda-z-3332-2026-beckman-coulter-mishima-k-k-systems-units"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-3324-2026",
   "date": "2026-10-07",
   "title": "Percussionaire Corporation: Travel Air recall",
   "firm": "Percussionaire Corporation",
   "product": "Travel Air, Product Number: S00055; Phasitron 5, Product Number: P5 used with Instruction Manual",
   "hazard": "Labeling updated warning not to use Intrapulmonary percussive ventilation (IPV) in conjunction with volatile anesthetic delivery systems because IPV may alter controlled delivery of volatile anesthetic agents, resulting in deeper/lighter anesthetic effects that may result in hypertonia/hypotonia, tachycardia/ bradycardia, elevated intracranial pressure, awareness during anesthesia, oversedation",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3324-2026%22",
   "url": "https://consumersun.com/recall/fda-z-3324-2026-percussionaire-corporation-travel-air"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-3271-2026",
   "date": "2026-10-07",
   "title": "Alere San Diego, Inc.: McKesson CONSULT hCG Urine Cassette recall",
   "firm": "Alere San Diego, Inc.",
   "product": "McKesson CONSULT hCG Urine Cassette, Model/ Part: FHC-A102/5001; Alere hCG Cassette (20 mIU/mL) in Urine, Model/ Part: FHC-A102/92210; Fisher Scientific Sure-Vue Serum/Urine¿hCG-STAT, Model/ Part: FHC-A202/23900531, FHC-A202/23900530; McKesson CONSULT Diagnostics hCG Urine Cassette, Model/ Part: FHC-A202/5002; Alere hCG Combo Cassette (20/10 mIU/mL) for Urine or Serum, Model/ Part: FHC-A202/92215; Cardinal Health hCG Combo Rapid Test Serum or Urine, Model/ Part: FHC-A202/B-1077-23; Medline hCG Combo Pregnancy Test Cassette, Model/ Part: FHC-A202/MPH22025HCG;",
   "hazard": "hCG rapid tests may detect low levels of hCG below the stated assay sensitivity, which may result in false positive result.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3271-2026%22",
   "url": "https://consumersun.com/recall/fda-z-3271-2026-alere-san-diego-inc-mckesson-consult-hcg-urine"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-3295-2026",
   "date": "2026-10-07",
   "title": "Cardinal Health 200, LLC: Presource Packs Containing Stryker StrykeFlow PS and AHTO tube sets: 1) KIT recall",
   "firm": "Cardinal Health 200, LLC",
   "product": "Presource Packs Containing Stryker StrykeFlow PS and AHTO tube sets: 1) KIT, LAP CHOLE , Catalog Number: PGCGLCBAC; 2) KIT, LAP CHOLE , Catalog Number: PGCGLCBAD; 3) KIT, LAP CHOLE , Catalog Number: PGCGLCBAE; 4) KIT, LAP CHOLE , Catalog Number: PGCGLCB11; 5) KIT, CARDIO MINIMALLY INVASIVE, Catalog Number: PV63CMST5; 6) HMC ROBOTIC PACK , Catalog Number: SBA23RBHNG; 7) HMC ROBOTIC PACK , Catalog Number: SBA23RBHNH; 8) ENS ENDOCHOLEYCYSTECTOMIE 4 , Catalog Number: SBA30EDCLB; 9) LAP CHOLE PACK , Catalog Number: SLC37LCJOB; 10) LAP CHOLE PACK , Catalog Number: SLC37LCJ21; 11) LAP CHOLE PACK , Catalog Number: SLC37LCJ22; 12) PACK GYNE ROBOTIC , Catalog Number: SMA30RBHSA",
   "hazard": "The kits contain tube sets with handpieces that may leak during use. The impacted devices can have the following failures: fluid leakage from the hand piece that can pool on the floor. The impact can range from user dissatisfaction to the potential for the user of slip and fall.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3295-2026%22",
   "url": "https://consumersun.com/recall/fda-z-3295-2026-cardinal-health-200-llc-presource-packs"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-0010-2027",
   "date": "2026-10-07",
   "title": "ASP Global, LLC.: Brand Name: Expressaire Product Name: DISPOSABLE TOURNIQUET CUFF recall",
   "firm": "ASP Global, LLC.",
   "product": "Brand Name: Expressaire Product Name: DISPOSABLE TOURNIQUET CUFF, 24\" X 4\" 1-LINE (CS 10) YELLOW Model/Catalog Number: 564008 Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. It is non-invasive device. Tourniquet Cuffs are intended for use in surgical procedures that requires the interruption of blood flow and clear visualization of the operative field. Component: No",
   "hazard": "Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0010-2027%22",
   "url": "https://consumersun.com/recall/fda-z-0010-2027-asp-global-llc-brand-name-expressaire-product"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-3330-2026",
   "date": "2026-10-07",
   "title": "Tandem Diabetes Care, Inc.: Brand Name: Tandem t:slim mobile application Product Name: t:slim Mobile Application recall",
   "firm": "Tandem Diabetes Care, Inc.",
   "product": "Brand Name: Tandem t:slim mobile application Product Name: t:slim Mobile Application, iOS Model/Catalog Number: iOS software version 2.13 Software Version: iOS software version 2.13 UDI-DI: 00389152470740 Component: No",
   "hazard": "A beta (early-release) version of the iOS application, version 2.13 (TestFlight) had a software issue preventing successful pairing of the t:slim application with Abbott FreeStyle Libre 3 Plus (FSL3P) continuous glucose monitoring (CGM) sensors, resulting in the insulin pump being unable to establish a near-field communication (NFC) connection with the CGM and requiring FSL3P users to use their t:slim insulin pumps in manual mode. FSL3P users are unable to access their CGM's glucose values from within the t:slim app and cannot use their pumps in automated control (closed-loop) mode, which could lead to users experiencing hypoglycemia or hyperglycemia.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3330-2026%22",
   "url": "https://consumersun.com/recall/fda-z-3330-2026-tandem-diabetes-care-inc-brand-name-tandem-t-slim"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-3292-2026",
   "date": "2026-10-07",
   "title": "American Contract Systems Inc: Medical convenience kits containing BD CliniClean Pericare Wipes within BD Urinary Cathete recall",
   "firm": "American Contract Systems Inc",
   "product": "Medical convenience kits containing BD CliniClean Pericare Wipes within BD Urinary Catheter Trays ROBOTIC PACK - 242561 Model No. MHRB88AO",
   "hazard": "Kits contain manufacturer-recalled perineal care (pericare) wipes within urinary catheter trays, which may be contaminated with a lubricant used during the manufacturing process. Use of a contaminated wipe may lead to localized skin effects such as irritation, erythema, or mild inflammation. Failure to perform pericare due to disposal of contaminated wipes may increase risk of localized infection or catheter-associated urinary tract infection (CAUTI).",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3292-2026%22",
   "url": "https://consumersun.com/recall/fda-z-3292-2026-american-contract-systems-inc-medical-convenience"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-3304-2026",
   "date": "2026-10-07",
   "title": "Heraeus Medical GmbH (Dental Division): PALACOS MV pro 40 recall",
   "firm": "Heraeus Medical GmbH (Dental Division)",
   "product": "PALACOS MV pro 40; PALACOS MV pro 80. Model/Catalog Number: 5150633; 5150635. Radiopaque, poly(methyl methacrylate)-based (PMMA) bone cement, pre-filled into a mixing and application system, suitable for use with or without vacuum (ready to mix). Component: N/A",
   "hazard": "Potential for monomer liquid leakage.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3304-2026%22",
   "url": "https://consumersun.com/recall/fda-z-3304-2026-heraeus-medical-gmbh-dental-division-palacos-mv"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-3302-2026",
   "date": "2026-10-07",
   "title": "Heraeus Medical GmbH (Dental Division): PALACOS R+G pro 40 recall",
   "firm": "Heraeus Medical GmbH (Dental Division)",
   "product": "PALACOS R+G pro 40; PALACOS R+G pro 80. Model/Catalog Number: 5081288; 5081289. Radiopaque, poly(methyl methacrylate)-based (PMMA) bone cement, pre-filled into a mixing and application system, suitable for use with or without vacuum (ready to mix).",
   "hazard": "Potential for monomer liquid leakage.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3302-2026%22",
   "url": "https://consumersun.com/recall/fda-z-3302-2026-heraeus-medical-gmbh-dental-division-palacos-r-g"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-0061-2027",
   "date": "2026-10-07",
   "title": "ASP Global, LLC.: Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 8\" 2 LINE (10) Model/Catalog Numbe recall",
   "firm": "ASP Global, LLC.",
   "product": "Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 8\" 2 LINE (10) Model/Catalog Number: DT-7108-02Q Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. It is non-invasive device. Tourniquet Cuffs are intended for use in surgical procedures that requires the interruption of blood flow and clear visualization of the operative field. Component: No",
   "hazard": "Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0061-2027%22",
   "url": "https://consumersun.com/recall/fda-z-0061-2027-asp-global-llc-brand-name-mpr-product-name-single"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-3283-2026",
   "date": "2026-10-07",
   "title": "Shanghai United Imaging Healthcare Co., Ltd.: Positron Emission Tomography and Computed Tomography System recall",
   "firm": "Shanghai United Imaging Healthcare Co., Ltd.",
   "product": "Positron Emission Tomography and Computed Tomography System, Model: uMI 550 with software",
   "hazard": "Positron emission tomography and computed tomography x-ray systems have a software problem when Split or Local function is enabled, and multiple RIS exams are merged into a single study, that prevents patient images from being visible on the Patient Administration interface, which may result in the need for rescans.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3283-2026%22",
   "url": "https://consumersun.com/recall/fda-z-3283-2026-shanghai-united-imaging-healthcare-co-ltd"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-0011-2027",
   "date": "2026-10-07",
   "title": "ASP Global, LLC.: Brand Name: Expressaire Product Name: DISPOSABLE TOURNIQUET CUFF recall",
   "firm": "ASP Global, LLC.",
   "product": "Brand Name: Expressaire Product Name: DISPOSABLE TOURNIQUET CUFF, 24\" X 4\" 2-LINE (CS 10) YELLOW Model/Catalog Number: 564009 Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. It is non-invasive device. Tourniquet Cuffs are intended for use in surgical procedures that requires the interruption of blood flow and clear visualization of the operative field. Component: No",
   "hazard": "Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0011-2027%22",
   "url": "https://consumersun.com/recall/fda-z-0011-2027-asp-global-llc-brand-name-expressaire-product"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-3270-2026",
   "date": "2026-10-07",
   "title": "HeartSine Technologies Ltd: HeartSine samaritan PAD (Public Access Defibrillator) recall",
   "firm": "HeartSine Technologies Ltd",
   "product": "HeartSine samaritan PAD (Public Access Defibrillator); HeartSine SAM 350P 350P US Device, US English - 2 Min CPR UDI-DI codes: 0506016712067 350P US Device, US English (American Airlines) - 2 Min CPR UDI-DI code: 0506016712207 350P US Device, US English with Gateway - 2 Min CPR UDI-DI code: 0506016712804 HeartSine SAM 360P 360P US Device, US English - 2 Min CPR UDI-DI code: 0506016712068 HeartSine SAM 450P SAM 450P US Device, US English (2 min CPR) UDI-DI code: 0506016712069",
   "hazard": "Products were distributed without the required Maintenance Supplement, which describes an extra check every 3 months in addition to the monthly check.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3270-2026%22",
   "url": "https://consumersun.com/recall/fda-z-3270-2026-heartsine-technologies-ltd-heartsine-samaritan"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-3335-2026",
   "date": "2026-10-07",
   "title": "Siemens Healthcare Diagnostics, Inc.: Atellica CH Revised C-Reactive Protein (RCRP) recall",
   "firm": "Siemens Healthcare Diagnostics, Inc.",
   "product": "Atellica CH Revised C-Reactive Protein (RCRP); Siemens Material Number (SMN): 11537223;",
   "hazard": "The potential for falsely elevated results.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3335-2026%22",
   "url": "https://consumersun.com/recall/fda-z-3335-2026-siemens-healthcare-diagnostics-inc-atellica-ch"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-3291-2026",
   "date": "2026-10-07",
   "title": "American Nitrile Operations Llc: Brand Name: Opportunity Pro Product Name: Opportunity Pro Model/Catalog Number: 72-50800 recall",
   "firm": "American Nitrile Operations Llc",
   "product": "Brand Name: Opportunity Pro Product Name: Opportunity Pro Model/Catalog Number: 72-50800, 72-50801,72-50802,72-50803,72-50804 Product Description: Blue Nitrile patient examination glove",
   "hazard": "Gloves may exhibit defects such as tears, missing fingers, and debris. Use of defective gloves may lead to healthcare personnel and patient exposure to infectious pathogens leading to infection or cross-contamination, or exposure to chemical agents leading to irritation or systemic toxicities.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3291-2026%22",
   "url": "https://consumersun.com/recall/fda-z-3291-2026-american-nitrile-operations-llc-brand-name"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-3321-2026",
   "date": "2026-10-07",
   "title": "Percussionaire Corporation: Intrapulmonary Percussive Ventilation recall",
   "firm": "Percussionaire Corporation",
   "product": "Intrapulmonary Percussive Ventilation, IPV-1C, Product Number: S00002-C; Phasitron 5, Product Number: P5 used with Instruction Manual",
   "hazard": "Labeling updated warning not to use Intrapulmonary percussive ventilation (IPV) in conjunction with volatile anesthetic delivery systems because IPV may alter controlled delivery of volatile anesthetic agents, resulting in deeper/lighter anesthetic effects that may result in hypertonia/hypotonia, tachycardia/ bradycardia, elevated intracranial pressure, awareness during anesthesia, oversedation",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3321-2026%22",
   "url": "https://consumersun.com/recall/fda-z-3321-2026-percussionaire-corporation-intrapulmonary"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-0032-2027",
   "date": "2026-10-07",
   "title": "ASP Global, LLC.: Brand Name: Expressaire Product Name:DISPOSABLE TOURNIQUET CUFF recall",
   "firm": "ASP Global, LLC.",
   "product": "Brand Name: Expressaire Product Name:DISPOSABLE TOURNIQUET CUFF, 34\" X 4\" 2-LINE (CS 18) BLUE Model/Catalog Number: A70107011 Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. It is non-invasive device. Tourniquet Cuffs are intended for use in surgical procedures that requires the interruption of blood flow and clear visualization of the operative field. Component: No",
   "hazard": "Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0032-2027%22",
   "url": "https://consumersun.com/recall/fda-z-0032-2027-asp-global-llc-brand-name-expressaire-product"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-0008-2027",
   "date": "2026-10-07",
   "title": "ASP Global, LLC.: Brand Name: Expressaire Product Name: DISPOSABLE TOURNIQUET CUFF recall",
   "firm": "ASP Global, LLC.",
   "product": "Brand Name: Expressaire Product Name: DISPOSABLE TOURNIQUET CUFF, 18\" X 4\" 1-LINE (CS 10) RED Model/Catalog Number: 564006 Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. It is non-invasive device. Tourniquet Cuffs are intended for use in surgical procedures that requires the interruption of blood flow and clear visualization of the operative field. Component: No",
   "hazard": "Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0008-2027%22",
   "url": "https://consumersun.com/recall/fda-z-0008-2027-asp-global-llc-brand-name-expressaire-product"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-0042-2027",
   "date": "2026-10-07",
   "title": "ASP Global, LLC.: Brand Name: ASP Global Product Name:DISPOSABLE TOURNIQUET CUFF recall",
   "firm": "ASP Global, LLC.",
   "product": "Brand Name: ASP Global Product Name:DISPOSABLE TOURNIQUET CUFF, 24\" X 4\" 2-Line, Yellow Model/Catalog Number: ASP-564009 Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. It is non-invasive device. Tourniquet Cuffs are intended for use in surgical procedures that requires the interruption of blood flow and clear visualization of the operative field. Component: No",
   "hazard": "Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0042-2027%22",
   "url": "https://consumersun.com/recall/fda-z-0042-2027-asp-global-llc-brand-name-asp-global-product-name"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-0066-2027",
   "date": "2026-10-07",
   "title": "ASP Global, LLC.: Brand Name: MPR Product Name:DISPOSABLE TOURNIQUET CUFF 18\" 2 LINE (10) Model/Catalog Numb recall",
   "firm": "ASP Global, LLC.",
   "product": "Brand Name: MPR Product Name:DISPOSABLE TOURNIQUET CUFF 18\" 2 LINE (10) Model/Catalog Number: DT-7218-02Q Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. It is non-invasive device. Tourniquet Cuffs are intended for use in surgical procedures that requires the interruption of blood flow and clear visualization of the operative field. Component: No",
   "hazard": "Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0066-2027%22",
   "url": "https://consumersun.com/recall/fda-z-0066-2027-asp-global-llc-brand-name-mpr-product-name"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-3317-2026",
   "date": "2026-10-07",
   "title": "Philips North America: Upgrade to MR 7700 recall",
   "firm": "Philips North America",
   "product": "Upgrade to MR 7700; Model number (REF): 782130; Software Versions: R11, R12 and R13;",
   "hazard": "When exporting diffusion tensor imaging (DTI) scans from a MR system using the Enhanced MR DICOM format, the exports contain incorrect data (diffusion directions). If the Enhanced MR DICOM export is used in conjunction with third-party software for tractography (e.g. for mapping nerve fiber pathways in the brain), the software will not be able to correctly process the DTI data for reconstruction.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3317-2026%22",
   "url": "https://consumersun.com/recall/fda-z-3317-2026-philips-north-america-upgrade-to-mr-7700"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-0047-2027",
   "date": "2026-10-07",
   "title": "ASP Global, LLC.: Brand Name: ASP Global Product Name:DISPOSABLE TOURNIQUET CUFF recall",
   "firm": "ASP Global, LLC.",
   "product": "Brand Name: ASP Global Product Name:DISPOSABLE TOURNIQUET CUFF, 44\" X 4\" 1-Line, Green Model/Catalog Number: ASP-564014 Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. It is non-invasive device. Tourniquet Cuffs are intended for use in surgical procedures that requires the interruption of blood flow and clear visualization of the operative field. Component: No",
   "hazard": "Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0047-2027%22",
   "url": "https://consumersun.com/recall/fda-z-0047-2027-asp-global-llc-brand-name-asp-global-product-name"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-0024-2027",
   "date": "2026-10-07",
   "title": "ASP Global, LLC.: Brand Name: Expressaire Product Name: DISPOSABLE TOURNIQUET CUFF recall",
   "firm": "ASP Global, LLC.",
   "product": "Brand Name: Expressaire Product Name: DISPOSABLE TOURNIQUET CUFF, 12\" X 3.5\" 2-LINE (CS 12) PLUM Model/Catalog Number: A70107003 Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. It is non-invasive device. Tourniquet Cuffs are intended for use in surgical procedures that requires the interruption of blood flow and clear visualization of the operative field. Component: No",
   "hazard": "Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0024-2027%22",
   "url": "https://consumersun.com/recall/fda-z-0024-2027-asp-global-llc-brand-name-expressaire-product"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-0058-2027",
   "date": "2026-10-07",
   "title": "ASP Global, LLC.: Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 34\" 2 LINE (10) Model/Catalog Numb recall",
   "firm": "ASP Global, LLC.",
   "product": "Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 34\" 2 LINE (10) Model/Catalog Number: DT-7034-02Q Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. It is non-invasive device. Tourniquet Cuffs are intended for use in surgical procedures that requires the interruption of blood flow and clear visualization of the operative field. Component: No",
   "hazard": "Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0058-2027%22",
   "url": "https://consumersun.com/recall/fda-z-0058-2027-asp-global-llc-brand-name-mpr-product-name-single"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-3288-2026",
   "date": "2026-10-07",
   "title": "Shanghai United Imaging Healthcare Co., Ltd.: Positron Emission Tomography and Computed Tomography System recall",
   "firm": "Shanghai United Imaging Healthcare Co., Ltd.",
   "product": "Positron Emission Tomography and Computed Tomography System, Model: uMI 780",
   "hazard": "Positron emission tomography and computed tomography x-ray systems have a software problem when Split or Local function is enabled, and multiple RIS exams are merged into a single study, that prevents patient images from being visible on the Patient Administration interface, which may result in the need for rescans.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3288-2026%22",
   "url": "https://consumersun.com/recall/fda-z-3288-2026-shanghai-united-imaging-healthcare-co-ltd"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-0030-2027",
   "date": "2026-10-07",
   "title": "ASP Global, LLC.: Brand Name: Expressaire Product Name:DISPOSABLE TOURNIQUET CUFF recall",
   "firm": "ASP Global, LLC.",
   "product": "Brand Name: Expressaire Product Name:DISPOSABLE TOURNIQUET CUFF, 24\" X 4\" 2-LINE (CS 18) YELLOW Model/Catalog Number: A70107009 Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. It is non-invasive device. Tourniquet Cuffs are intended for use in surgical procedures that requires the interruption of blood flow and clear visualization of the operative field. Component: No",
   "hazard": "Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0030-2027%22",
   "url": "https://consumersun.com/recall/fda-z-0030-2027-asp-global-llc-brand-name-expressaire-product"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-0031-2027",
   "date": "2026-10-07",
   "title": "ASP Global, LLC.: Brand Name: Expressaire Product Name:DISPOSABLE TOURNIQUET CUFF recall",
   "firm": "ASP Global, LLC.",
   "product": "Brand Name: Expressaire Product Name:DISPOSABLE TOURNIQUET CUFF, 34\" X 4\" 1-LINE (CS 18) BLUE Model/Catalog Number: A70107010 Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. It is non-invasive device. Tourniquet Cuffs are intended for use in surgical procedures that requires the interruption of blood flow and clear visualization of the operative field. Component: No",
   "hazard": "Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0031-2027%22",
   "url": "https://consumersun.com/recall/fda-z-0031-2027-asp-global-llc-brand-name-expressaire-product"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-0054-2027",
   "date": "2026-10-07",
   "title": "ASP Global, LLC.: Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 24\" 2 LINE (10) Model/Catalog Numb recall",
   "firm": "ASP Global, LLC.",
   "product": "Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 24\" 2 LINE (10) Model/Catalog Number: DT-7024-02Q Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. It is non-invasive device. Tourniquet Cuffs are intended for use in surgical procedures that requires the interruption of blood flow and clear visualization of the operative field. Component: No",
   "hazard": "Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0054-2027%22",
   "url": "https://consumersun.com/recall/fda-z-0054-2027-asp-global-llc-brand-name-mpr-product-name-single"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-3273-2026",
   "date": "2026-10-07",
   "title": "Alere San Diego, Inc.: Fisher Scientific Sure-Vue Urine hCG Strip recall",
   "firm": "Alere San Diego, Inc.",
   "product": "Fisher Scientific Sure-Vue Urine hCG Strip, Model/ Part: FHC-101/23900527; McKesson CONSULT hCG Urine Test Dipstick CLIA Waived, Model/ Part:FHC-101/5000; Henry Schein One Step+ hCG Urine Strip Test, Model/ Part: FHC-101/9004072; Alere hCG Dipstick (25mIU/mL) in Urine, Model/ Part: FHC-101/92211; Cardinal Health hCG Dipstick Rapid Test CLIA Waived, Model/ Part: FHC-101/B-1077-21; Medline hCG Pregnancy Test Strip, Model/ Part: FHC-101/MPH11025HCG; Pro Advantage by NDC Urine Pregnancy Test Strip, Model/ Part: FHC-101/P080023;",
   "hazard": "hCG rapid tests may detect low levels of hCG below the stated assay sensitivity, which may result in false positive result.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3273-2026%22",
   "url": "https://consumersun.com/recall/fda-z-3273-2026-alere-san-diego-inc-fisher-scientific-sure-vue"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-0034-2027",
   "date": "2026-10-07",
   "title": "ASP Global, LLC.: Brand Name: Expressaire Product Name:DISPOSABLE TOURNIQUET CUFF recall",
   "firm": "ASP Global, LLC.",
   "product": "Brand Name: Expressaire Product Name:DISPOSABLE TOURNIQUET CUFF, 44\" X 4\" 2-LINE (CS 12) GREEN Model/Catalog Number: A70107013 Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. It is non-invasive device. Tourniquet Cuffs are intended for use in surgical procedures that requires the interruption of blood flow and clear visualization of the operative field. Component: No",
   "hazard": "Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0034-2027%22",
   "url": "https://consumersun.com/recall/fda-z-0034-2027-asp-global-llc-brand-name-expressaire-product"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-0048-2027",
   "date": "2026-10-07",
   "title": "ASP Global, LLC.: Brand Name: ASP Global Product Name:DISPOSABLE TOURNIQUET CUFF recall",
   "firm": "ASP Global, LLC.",
   "product": "Brand Name: ASP Global Product Name:DISPOSABLE TOURNIQUET CUFF, 44\" X 4\" 2-Line, Green Model/Catalog Number: ASP-564015 Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. It is non-invasive device. Tourniquet Cuffs are intended for use in surgical procedures that requires the interruption of blood flow and clear visualization of the operative field. Component: No",
   "hazard": "Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0048-2027%22",
   "url": "https://consumersun.com/recall/fda-z-0048-2027-asp-global-llc-brand-name-asp-global-product-name"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-3319-2026",
   "date": "2026-10-07",
   "title": "Percussionaire Corporation: Intrapulmonary Percussive Ventilation recall",
   "firm": "Percussionaire Corporation",
   "product": "Intrapulmonary Percussive Ventilation, IPV 1, Product Number: S00065; Phasitron 5 Breathing Circuit with Unified Connector, Product Number: P5-UC, used with In-Line Valve Instruction Manual",
   "hazard": "Labeling updated warning not to use Intrapulmonary percussive ventilation (IPV) in conjunction with volatile anesthetic delivery systems because IPV may alter controlled delivery of volatile anesthetic agents, resulting in deeper/lighter anesthetic effects that may result in hypertonia/hypotonia, tachycardia/ bradycardia, elevated intracranial pressure, awareness during anesthesia, oversedation",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3319-2026%22",
   "url": "https://consumersun.com/recall/fda-z-3319-2026-percussionaire-corporation-intrapulmonary"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-3301-2026",
   "date": "2026-10-07",
   "title": "Heraeus Medical GmbH (Dental Division): PALACOS R pro 40 recall",
   "firm": "Heraeus Medical GmbH (Dental Division)",
   "product": "PALACOS R pro 40; PALACOS R pro 80. Model/Catalog Numbers: 5081286; 5081287. Radiopaque, poly (methyl methacrylate)-based (PMMA) bone cement, pre-filled into a mixing and application system, suitable for use with or without vacuum (ready to mix).",
   "hazard": "Potential for monomer liquid leakage.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3301-2026%22",
   "url": "https://consumersun.com/recall/fda-z-3301-2026-heraeus-medical-gmbh-dental-division-palacos-r"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-3306-2026",
   "date": "2026-10-07",
   "title": "NOXBOX LTD: NOxBOXi Nitric Oxide Delivery System recall",
   "firm": "NOXBOX LTD",
   "product": "NOxBOXi Nitric Oxide Delivery System. Model Number: NOXBOX-I.",
   "hazard": "Potential for irregular oxygen readings due to a manufacturing issue affecting certain oxygen sensors.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3306-2026%22",
   "url": "https://consumersun.com/recall/fda-z-3306-2026-noxbox-ltd-noxboxi-nitric-oxide-delivery-system"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-0023-2027",
   "date": "2026-10-07",
   "title": "ASP Global, LLC.: Brand Name: Expressaire Product Name: DISPOSABLE TOURNIQUET CUFF recall",
   "firm": "ASP Global, LLC.",
   "product": "Brand Name: Expressaire Product Name: DISPOSABLE TOURNIQUET CUFF, 12\" X 3.5\" 1-LINE (CS 12) PLUM Model/Catalog Number: A70107002 Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. It is non-invasive device. Tourniquet Cuffs are intended for use in surgical procedures that requires the interruption of blood flow and clear visualization of the operative field. Component: No",
   "hazard": "Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0023-2027%22",
   "url": "https://consumersun.com/recall/fda-z-0023-2027-asp-global-llc-brand-name-expressaire-product"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-0064-2027",
   "date": "2026-10-07",
   "title": "ASP Global, LLC.: Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 15\" 1 LINE (10) Model/Catalog Numb recall",
   "firm": "ASP Global, LLC.",
   "product": "Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 15\" 1 LINE (10) Model/Catalog Number: DT-7115-01Q Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. It is non-invasive device. Tourniquet Cuffs are intended for use in surgical procedures that requires the interruption of blood flow and clear visualization of the operative field. Component: No",
   "hazard": "Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0064-2027%22",
   "url": "https://consumersun.com/recall/fda-z-0064-2027-asp-global-llc-brand-name-mpr-product-name-single"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-0041-2027",
   "date": "2026-10-07",
   "title": "ASP Global, LLC.: Brand Name: ASP Global Product Name:DISPOSABLE TOURNIQUET CUFF recall",
   "firm": "ASP Global, LLC.",
   "product": "Brand Name: ASP Global Product Name:DISPOSABLE TOURNIQUET CUFF, 24\" X 4\" 1-Line, Yellow Model/Catalog Number: ASP-564008 Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. It is non-invasive device. Tourniquet Cuffs are intended for use in surgical procedures that requires the interruption of blood flow and clear visualization of the operative field. Component: No",
   "hazard": "Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0041-2027%22",
   "url": "https://consumersun.com/recall/fda-z-0041-2027-asp-global-llc-brand-name-asp-global-product-name"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-3333-2026",
   "date": "2026-10-07",
   "title": "Karl Storz Endoscopy: HOPKINS Telescope 30¿ recall",
   "firm": "Karl Storz Endoscopy",
   "product": "HOPKINS Telescope 30¿, 4mm REF 10005BA UDI-DI code: 04048551045121 KARL STORZ HOPKINS¿ and HOPKINS¿ II telescopes are to be used for visualization of the surgical site during diagnostic and therapeutic endoscopic procedures.",
   "hazard": "Due to incorrect inside packaging label for eyepiece.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3333-2026%22",
   "url": "https://consumersun.com/recall/fda-z-3333-2026-karl-storz-endoscopy-hopkins-telescope-30"
  },
  {
   "agency": "FDA",
   "recall_id": "Z-3314-2026",
   "date": "2026-10-07",
   "title": "Philips North America: SmartPath to dStream for 1 recall",
   "firm": "Philips North America",
   "product": "SmartPath to dStream for 1.5T, SmartPath to dStream for 3.0T, SmartPath to dStream for XR and 3.0T, and SmartPath to Ingenia Elition X; Model number (REF): 1. 781260 (1.5T), 2. 782112 (1.5T), 3. 782146 (1.5T), 4. 782165 (1.5T), 5. 782145 (3.0T), 6. 782164 (3.0T), 7. 781270 (XR and 3.0T), 8. 782113 (XR and 3.0T), 9. 782129 (XR and 3.0T), 10. 782118 (Ingenia Elition X), 11. 782144 (Ingenia Elition X), 12. 782163 (Ingenia Elition X); Software Versions: R11, R12 and R13;",
   "hazard": "When exporting diffusion tensor imaging (DTI) scans from a MR system using the Enhanced MR DICOM format, the exports contain incorrect data (diffusion directions). If the Enhanced MR DICOM export is used in conjunction with third-party software for tractography (e.g. for mapping nerve fiber pathways in the brain), the software will not be able to correctly process the DTI data for reconstruction.",
   "remedy": null,
   "categories": [
    "health"
   ],
   "agency_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3314-2026%22",
   "url": "https://consumersun.com/recall/fda-z-3314-2026-philips-north-america-smartpath-to-dstream-for-1"
  },
  {
   "agency": "NHTSA",
   "recall_id": "26V652000",
   "date": "2026-10-06",
   "title": "E-One Incorporated: Wire Harness and Busbar May Overheat",
   "firm": "E-One Incorporated",
   "product": "2024-2026 Typhoon N, 2025-2026 Cyclone N, and 2026 Cyclone II fire trucks",
   "hazard": "An overheated busbar can increase the risk of a fire.",
   "remedy": "E-ONE will provide a replacement wiring harness and busbar, free of charge. Owner notification letters are expected to be mailed October 20, 2026. Owners may contact E-One customer service at 1-352-237-1122.",
   "categories": [
    "vehicles"
   ],
   "agency_url": "https://www.nhtsa.gov/recalls?nhtsaId=26V652000",
   "url": "https://consumersun.com/recall/nhtsa-26v652000-e-one-incorporated-wire-harness-and-busbar-may"
  },
  {
   "agency": "NHTSA",
   "recall_id": "26V647000",
   "date": "2026-10-05",
   "title": "Forest River, Inc.: Exterior Outlet May Lack GFCI Protection",
   "firm": "Forest River, Inc.",
   "product": "2027 Surveyor recreational trailers",
   "hazard": "An outlet without GFCI protection may fail to shut off electrical power when a ground-fault occurs, increasing the risk of injury.",
   "remedy": "Dealers will rewire the exterior outlet, free of charge. Owners may contact Forest River customer service at 1-574-642-3119. Forest River's number for this recall is 37-2103.",
   "categories": [
    "vehicles"
   ],
   "agency_url": "https://www.nhtsa.gov/recalls?nhtsaId=26V647000",
   "url": "https://consumersun.com/recall/nhtsa-26v647000-forest-river-inc-exterior-outlet-may-lack-gfci"
  },
  {
   "agency": "NHTSA",
   "recall_id": "26V646000",
   "date": "2026-10-05",
   "title": "Forest River, Inc.: Incorrect Tire Inflation on Federal Placard",
   "firm": "Forest River, Inc.",
   "product": "2026-2027 Sunseeker, Solera, and Forester recreational vehicles",
   "hazard": "A tire can be overinflated after referencing the incorrect information, increasing the risk of a crash.",
   "remedy": "Dealers will replace the labels, free of charge. Owner notification letters are expected to be mailed December 4, 2026. Owners may contact Forest River customer service at 1-574-206-7600. Forest River's number for this recall is 34-2102.",
   "categories": [
    "vehicles"
   ],
   "agency_url": "https://www.nhtsa.gov/recalls?nhtsaId=26V646000",
   "url": "https://consumersun.com/recall/nhtsa-26v646000-forest-river-inc-incorrect-tire-inflation-on"
  },
  {
   "agency": "NHTSA",
   "recall_id": "26V643000",
   "date": "2026-10-05",
   "title": "Greenpower Motor Company Inc.: Bus May Move with Wheelchair Lift Deployed",
   "firm": "Greenpower Motor Company Inc.",
   "product": "2021 Nano Beast school buses",
   "hazard": "The bus moving while the wheelchair lift is in use increases the risk of injury.",
   "remedy": "Dealers will update the control module software, free of charge. Owner notification letters are expected to be mailed October 12, 2026. Owners may contact Greenpower's customer service at 1-909-346-1090. Greenpower's number for this recall is GP2604002.",
   "categories": [
    "vehicles"
   ],
   "agency_url": "https://www.nhtsa.gov/recalls?nhtsaId=26V643000",
   "url": "https://consumersun.com/recall/nhtsa-26v643000-greenpower-motor-company-inc-bus-may-move-with"
  },
  {
   "agency": "NHTSA",
   "recall_id": "26E069000",
   "date": "2026-10-02",
   "title": "Roadmaster Inc.: Tow Bar May Separate from Hitch Receiver",
   "firm": "Roadmaster Inc.",
   "product": "Blackhawk All Terrain, Falcon 2, Falcon All Terrain, Falcon 3HD, Liberty, Sterling, and Nighthawk tow bars",
   "hazard": "A separated tow bar can result in the tow vehicle detaching, increases the risk of a crash.",
   "remedy": "Dealers will install a security band or replace the T-bolt assembly, free of charge. Owner notification letters are expected to be mailed October 2026. Owners may contact Roadmaster customer service at 1-800-669-9690. Roadmaster's number for this recall is 910-RPR.",
   "categories": [
    "vehicles"
   ],
   "agency_url": "https://www.nhtsa.gov/recalls?nhtsaId=26E069000",
   "url": "https://consumersun.com/recall/nhtsa-26e069000-roadmaster-inc-tow-bar-may-separate-from-hitch"
  },
  {
   "agency": "NHTSA",
   "recall_id": "26V642000",
   "date": "2026-10-02",
   "title": "Blue Bird Body Company: High Voltage Battery Mounting Bolts May Be Loose or Missing",
   "firm": "Blue Bird Body Company",
   "product": "2022-2024 All American Electric transit buses",
   "hazard": "A high voltage battery with loose or missing mounting bolts can cause a loss of drive power, increasing the risk of a crash.",
   "remedy": "Dealers will inspect and reinstall bolts with thread locker. Damaged or missing bolts will be replaced. All repairs will be performed free of charge. Owner notification letters are expected to be mailed December 1, 2026. Owners may contact Blue Bird customer service at 1-478-822-2242. Blue Bird's number for this recall is R26AK.",
   "categories": [
    "vehicles"
   ],
   "agency_url": "https://www.nhtsa.gov/recalls?nhtsaId=26V642000",
   "url": "https://consumersun.com/recall/nhtsa-26v642000-blue-bird-body-company-high-voltage-battery"
  },
  {
   "agency": "NHTSA",
   "recall_id": "26V641000",
   "date": "2026-10-02",
   "title": "Blue Bird Body Company: High Voltage Battery Mounting Bolts May Be Loose or Missing",
   "firm": "Blue Bird Body Company",
   "product": "2018-2024, 2026 Vision and All American Electric school buses",
   "hazard": "A high voltage battery with loose or missing mounting bolts can cause a loss of drive power, increasing the risk of a crash.",
   "remedy": "Dealers will inspect and reinstall bolts with thread locker. Damaged or missing bolts will be replaced. All repairs will be performed free of charge. Owner notification letters are expected to be mailed December 1, 2026. Owners may contact Blue Bird customer service at 1-478-822-2242. Blue Bird's number for this recall is R26AK.",
   "categories": [
    "vehicles"
   ],
   "agency_url": "https://www.nhtsa.gov/recalls?nhtsaId=26V641000",
   "url": "https://consumersun.com/recall/nhtsa-26v641000-blue-bird-body-company-high-voltage-battery"
  },
  {
   "agency": "NHTSA",
   "recall_id": "26V640000",
   "date": "2026-10-02",
   "title": "Rosenbauer America: Do Not Drive: Cracked Weld May Cause Wheel and/or Tire Failure",
   "firm": "Rosenbauer America",
   "product": "2024-2025 Commander and 2024 Warrior fire engines",
   "hazard": "Wheel and/or tire failure increases the risk of a crash.",
   "remedy": "Owners are advised not to drive their vehicles until the remedy has been completed. Dealers will replace the wheels and tires as necessary, free of charge. Owner notification letters are expected to be mailed October 19, 2026. Owners may contact Rosenbauer customer service at 1-651-462-1000.",
   "categories": [
    "vehicles"
   ],
   "agency_url": "https://www.nhtsa.gov/recalls?nhtsaId=26V640000",
   "url": "https://consumersun.com/recall/nhtsa-26v640000-rosenbauer-america-do-not-drive-cracked-weld-may"
  },
  {
   "agency": "NHTSA",
   "recall_id": "26V639000",
   "date": "2026-10-02",
   "title": "Ring Power Corporation: Rear Bumper Hitch Plate May Bend",
   "firm": "Ring Power Corporation",
   "product": "2020 Terex General 65, 2020-2021 C6000, 2020-2022 C4000, and TC55 vehicles",
   "hazard": "The pintle hitch may fail, causing a loss of trailer control and increasing the risk of a crash.",
   "remedy": "Ring Power will inspect, replace the pintle hitch, and install bracing. Damaged bumpers will be replaced. All repairs will be performed free of charge. Owner notification letters are expected to be mailed October 16, 2026. Owners may contact Ring Power's customer service at 904-613-0035. Ring Power's number for this recall is 23402.",
   "categories": [
    "vehicles"
   ],
   "agency_url": "https://www.nhtsa.gov/recalls?nhtsaId=26V639000",
   "url": "https://consumersun.com/recall/nhtsa-26v639000-ring-power-corporation-rear-bumper-hitch-plate"
  },
  {
   "agency": "NHTSA",
   "recall_id": "26V638000",
   "date": "2026-10-02",
   "title": "Mercedes-Benz USA, LLC: Front Brake Hose May Leak",
   "firm": "Mercedes-Benz USA, LLC",
   "product": "2022-2025 S 500 4MATIC, Maybach S 580 4MATIC, Maybach S 680 4MATIC, S 580 4MATIC, 2023-2025 S 580 E 4MATIC, and 2024-2025 AMG S 63 E Performance vehicles",
   "hazard": "A brake fluid leak can extend the distance needed to stop the vehicle, increasing the risk of a crash.",
   "remedy": "Dealers will replace the front brake hoses, free of charge. Owner notification letters are expected to be mailed November 27, 2026. Owners may contact MBUSA customer service at 1-800-367-6372. This recall expands previous NHTSA recall number 25V116. Vehicle Identification Numbers (VINs) involved in this recall became searchable on NHTSA.gov on October 9, 2026.",
   "categories": [
    "vehicles"
   ],
   "agency_url": "https://www.nhtsa.gov/recalls?nhtsaId=26V638000",
   "url": "https://consumersun.com/recall/nhtsa-26v638000-mercedes-benz-usa-llc-front-brake-hose-may-leak"
  },
  {
   "agency": "NHTSA",
   "recall_id": "26V637000",
   "date": "2026-10-02",
   "title": "Altec Industries, Inc.: Platform Access Step May Separate from Vehicle",
   "firm": "Altec Industries, Inc.",
   "product": "2020-2026 AA Series Aerial Device, 2021-2026 AN Series Aerial Device, 2023-2026 AM Series Aerial Device, and 2024-2026 Digger Derrick, and 2024-2025 A-Class vehicles",
   "hazard": "A step that separates or becomes unstable while in use, increases the risk of a fall or injury.",
   "remedy": "Altec will replace the steps, free of charge. Owner notification letters are expected to be mailed November 27, 2026. Owners may contact Altec's customer service at 1-877-462-5832. Altec's number for this recall is CSN-3374.",
   "categories": [
    "vehicles"
   ],
   "agency_url": "https://www.nhtsa.gov/recalls?nhtsaId=26V637000",
   "url": "https://consumersun.com/recall/nhtsa-26v637000-altec-industries-inc-platform-access-step-may"
  },
  {
   "agency": "NHTSA",
   "recall_id": "26V636000",
   "date": "2026-10-02",
   "title": "Mercedes-Benz USA, LLC: Improperly Installed Seat Belt Component",
   "firm": "Mercedes-Benz USA, LLC",
   "product": "2027 CLA 220 vehicles",
   "hazard": "A seat belt with an incorrectly installed component may fail to properly restrain occupants, increasing the risk of injury during a crash.",
   "remedy": "Dealers will inspect and replace the seat belt as necessary, free of charge. Owner notification letters are expected to be mailed November 27, 2026. Owners may contact MBUSA customer service at 1-800-367-6372.",
   "categories": [
    "vehicles"
   ],
   "agency_url": "https://www.nhtsa.gov/recalls?nhtsaId=26V636000",
   "url": "https://consumersun.com/recall/nhtsa-26v636000-mercedes-benz-usa-llc-improperly-installed-seat"
  },
  {
   "agency": "CPSC",
   "recall_id": "27003",
   "date": "2026-10-01",
   "title": "ABC Trading Recalls Squishy Toys Due to Risk of Serious Injury or Death from Water Bead Ingestion; Violate Mandatory Standard for Toys",
   "firm": "ABC Trading Inc., of Vernon, California",
   "product": "Squishy Dumpling Toys, Crazy Squib Ball Toys",
   "hazard": "The squishy toys violate the mandatory safety standard for toys because the water beads inside the toys expand larger than permitted, posing a deadly ingestion hazard. If a water bead is ingested, it can pose ingestion, choking, and intestinal obstruction hazards inside a child's body, resulting in severe discomfort, vomiting, dehydration and a risk of death to a child.",
   "remedy": "Consumers should stop using the squishy toys immediately and contact ABC Trading for a full refund. Consumers will be asked to write \"RECALLED\" in permanent marker on the squishy toys, throw the toy away and email a photo of the disposed toy to recallabc@gmail.com.",
   "categories": [
    "baby"
   ],
   "agency_url": "https://www.cpsc.gov/Recalls/2027/ABC-Trading-Recalls-Squishy-Toys-Due-to-Risk-of-Serious-Injury-or-Death-from-Water-Bead-Ingestion-Violate-Mandatory-Standard-for-Toys",
   "url": "https://consumersun.com/recall/cpsc-27003-squishy-toys"
  },
  {
   "agency": "CPSC",
   "recall_id": "27014",
   "date": "2026-10-01",
   "title": "Agrish Reannounces and Expands Recall of Adult Portable Bed Rails Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violate Mandatory Standard for Adult Portable Bed Rails; Additional Units Added",
   "firm": "Zhongshan Lebo Medical Co., Ltd., of China",
   "product": "Agrish Adult Portable Bed Rails, models 12014, AG-12011 and 12016",
   "hazard": "The recalled bed rails violate the mandatory standard for adult portable bed rails because when the bed rails are attached to a bed, users can become entrapped within the bed rail or between the bed rail and the side of the mattress, posing a serious entrapment hazard and risk of death by asphyxiation. The bed rails do not meet structural stability or retention strap requirements, posing a fall hazard. Additionally, the bed rails' push pins and push pin holes are incorrectly sized, posing a laceration hazard.",
   "remedy": "Consumers should immediately stop using the recalled adult portable bed rails and contact Agrish Direct for a full refund. Consumers will be asked to go to http://www.agrish.online/recall to register for the recall and receive instructions on how to dispose of the recalled bed rail.",
   "categories": [
    "home"
   ],
   "agency_url": "https://cpsc.gov/Recalls/2027/Agrish-Reannounces-and-Expands-Recall-of-Adult-Portable-Bed-Rails-Due-to-Risk-of-Serious-Injury-or-Death-from-Entrapment-and-Asphyxiation-Violate-Mandatory-Standard-for-Adult-Portable-Bed-Rails-Additional-Units-Added",
   "url": "https://consumersun.com/recall/cpsc-27014-of-adult-portable-bed-rails"
  },
  {
   "agency": "CPSC",
   "recall_id": "27007",
   "date": "2026-10-01",
   "title": "Designs Direct Recalls Cupcakes and Cashmere Brand Three-Light Floor Lamps, Due to Risk of Serious Injury from Fire and Burn Hazards",
   "firm": "Designs Direct LLC, d/b/a Designs Direct Creative Group, of Covington, Kentucky",
   "product": "Designs Direct Cupcakes and Cashmere Brand Three-Light Floor Lamps",
   "hazard": "When plugged in or switched on, the lamp cord or internal wiring can smoke, melt, spark, overheat or ignite, posing a risk of serious injury from fire and burn hazards.",
   "remedy": "Consumers should stop using the recalled lamp immediately, turn it off, and unplug it. Consumers will be asked to cut the cord and provide a photograph of the destroyed lamp, following the instructions at https://www.designsdirectllc.com/recalls/. Designs Direct will issue a full refund to consumers within 15 days of receipt of the photo proof of destruction.",
   "categories": [
    "electronics",
    "home"
   ],
   "agency_url": "https://cpsc.gov/Recalls/2027/Designs-Direct-Recalls-Cupcakes-and-Cashmere-Brand-Three-Light-Floor-Lamps-Due-to-Risk-of-Serious-Injury-from-Fire-and-Burn-Hazards",
   "url": "https://consumersun.com/recall/cpsc-27007-cupcakes-and-cashmere-brand-three-light-floor"
  },
  {
   "agency": "CPSC",
   "recall_id": "27012",
   "date": "2026-10-01",
   "title": "Dollar Tree Stores Recalls Electric Balloon Pumps Due to Burn Hazard",
   "firm": "Dollar Tree Stores, Inc. (\"Dollar Tree\") of Chesapeake, Virginia",
   "product": "Electric Balloon Pumps",
   "hazard": "The recalled electric balloon pumps can overheat, posing a burn hazard.",
   "remedy": "Consumers should stop using the recalled electric balloon pumps immediately and return it to any Dollar Tree store to receive a full refund. Consumers who purchased the electric balloon pump online should contact the firm to receive a pre-paid shipping label to return the recalled product to receive a full refund.",
   "categories": [
    "electronics",
    "home"
   ],
   "agency_url": "https://www.cpsc.gov/Recalls/2027/Dollar-Tree-Stores-Recalls-Electric-Balloon-Pumps-Due-to-Burn-Hazard",
   "url": "https://consumersun.com/recall/cpsc-27012-electric-balloon-pumps"
  },
  {
   "agency": "CPSC",
   "recall_id": "27004",
   "date": "2026-10-01",
   "title": "Gazelle USA Recalls Urban Arrow Cargo Electric Bikes Due to Fall Hazard",
   "firm": "Gazelle USA LLC, of Santa Cruz, California",
   "product": "Urban Arrow Cargo Electric Bikes",
   "hazard": "The front bolt in the seat post clamping mechanism can break, causing the seat to become loose, posing a fall hazard.",
   "remedy": "Consumers should stop using the recalled bicycles immediately and contact Gazelle USA to receive a free replacement seat post and saddle that consumers can either install themselves with no special tools or take to an Urban Arrow dealer to be installed at no charge. Consumers will be asked to fill out a recall registration form at https://forms.gle/1Nir9NrR7aJcpwRk8. Consumers can locate their nearest dealer at https://urbanarrow.com/dealers.",
   "categories": [
    "electronics",
    "home"
   ],
   "agency_url": "https://www.cpsc.gov/Recalls/2027/Gazelle-USA-Recalls-Urban-Arrow-Cargo-Electric-Bikes-Due-to-Fall-Hazard",
   "url": "https://consumersun.com/recall/cpsc-27004-urban-arrow-cargo-electric-bikes"
  },
  {
   "agency": "CPSC",
   "recall_id": "27008",
   "date": "2026-10-01",
   "title": "GBYMIUY Recalls Magnetic Stick Figure Toy Sets Due to Risk of Serious Injury or Death from Magnet Ingestion; Violate Mandatory Standard for Toys",
   "firm": "Ningbo Jiboyou Trading Co., Ltd. dba GBYMIUY, of China",
   "product": "GBYMIUY Magnetic Stick Figure Toy Sets",
   "hazard": "The magnetic stick figure toy sets violate the mandatory standard for toys because they can liberate loose high-powered magnets posing an ingestion hazard to children. When high-powered magnets are swallowed, the ingested magnets can attract each other or other metal objects and become lodged in the digestive system. This can result in perforations, twisting, and/or blockage of the intestines, blood poisoning and death.",
   "remedy": "Consumers should take the stick figures away from children immediately, stop using them and contact GBYMIUY for a full refund. Consumers will be asked to throw away the stick figure toys and send a photo of the disposed toys to zhangfa0426@outlook.com.",
   "categories": [
    "baby"
   ],
   "agency_url": "https://cpsc.gov/Recalls/2027/GBYMIUY-Recalls-Magnetic-Stick-Figure-Toy-Sets-Due-to-Risk-of-Serious-Injury-or-Death-from-Magnet-Ingestion-Violate-Mandatory-Standard-for-Toys",
   "url": "https://consumersun.com/recall/cpsc-27008-magnetic-stick-figure-toy-sets"
  },
  {
   "agency": "CPSC",
   "recall_id": "27009",
   "date": "2026-10-01",
   "title": "Gobi Heat Recalls Rechargeable Hand Warmers Due to Risk of Serious Injury from Fire and Burn Hazards",
   "firm": "Dragon Gear Inc., dba Gobi Heat, of Severance, Colorado",
   "product": "Gobi Heat Rechargeable Hand Warmers",
   "hazard": "The lithium-ion battery and electrical components in the recalled hand warmers can overheat and ignite, posing a risk of serious injury from fire and burn hazards.",
   "remedy": "Consumers should stop using the recalled hand warmers immediately and contact Gobi Heat for a full refund or store credit, equal to full refund of the purchase price plus 20% of that amount. Consumers will be asked to go to https://gobiheat.com/pages/handwarmer-recall to obtain a claim number and instructions to destroy the hand warmers by writing in permanent marker \"Recalled\" on the product and send a photo, showing the marked hand warmer and the product's model, to recall@gobiheat.com. Consumers should then dispose of the recalled product with the lithium-ion battery, in accordance with applicable local and state hazardous waste regulations. Note: Do not throw this recalled lithium-ion battery or device in the trash, the general recycling stream (e.g., street-level or curbside recycling bins), or used battery recycling boxes found at various retail and home improvement stores. Recalled lithium-ion batteries must be disposed of differently than other batteries, because they present a greater risk of fire. Your municipal household hazardous waste (HHW) collection center may accept this recalled lithium-ion battery or device for disposal. Before taking your battery or device to a HHW collection center, contact that office ahead of time and ask whether it accepts recalled lithium-ion batteries. If it does not, contact your municipality for further guidance.",
   "categories": [
    "electronics",
    "home"
   ],
   "agency_url": "https://www.cpsc.gov/Recalls/2027/Gobi-Heat-Recalls-Rechargeable-Hand-Warmers-Due-to-Risk-of-Serious-Injury-from-Fire-and-Burn-Hazards",
   "url": "https://consumersun.com/recall/cpsc-27009-rechargeable-hand-warmers"
  },
  {
   "agency": "CPSC",
   "recall_id": "27013",
   "date": "2026-10-01",
   "title": "Golden Resale Recalls Portable Camping Showers Due to Risk of Serious Injury or Death from Fire Hazard",
   "firm": "Golden Resale LLC, of Mesa, Arizona",
   "product": "Portable Camping Showers with bucket and immersion heater",
   "hazard": "The recalled camping showers' immersion heaters can quickly ignite when they are partially or completely out of water, posing a risk of serious injury or death from a fire hazard.",
   "remedy": "Consumers should stop using the Portable Camping Showers immediately and contact Golden Resale toll-free at 855-927-2440 for a full refund. The refund process will be initiated through Amazon or Walmart's return systems. If consumers decide to continue with the full refund process, they will be sent a free pre-paid package to return the recalled camping showers to Golden Resale. Once the return is processed, the customers will receive the refund in the same form of payment as they used for their original purchase.",
   "categories": [
    "electronics",
    "home"
   ],
   "agency_url": "https://www.cpsc.gov/Recalls/2027/Golden-Resale-Recalls-Portable-Camping-Showers-Due-to-Risk-of-Serious-Injury-or-Death-from-Fire-Hazard",
   "url": "https://consumersun.com/recall/cpsc-27013-portable-camping-showers"
  },
  {
   "agency": "CPSC",
   "recall_id": "27011",
   "date": "2026-10-01",
   "title": "Kobayashi Recalls Rechargeable Hand Warmers Due to Risk of Serious Injury from Fire and Burn Hazards",
   "firm": "Kobayashi Consumer Products, LLC, of Dalton, Georgia",
   "product": "HotHands® Rechargeable Hand Warmers",
   "hazard": "The lithium-ion battery and electrical components in the recalled hand warmers can overheat and ignite, posing a risk of serious injury from fire and burn hazards.",
   "remedy": "Consumers should stop using the recalled hand warmers immediately and contact Kobayashi for a full refund. Consumers will be asked to go to https://hothands.com/recall-notice-rechargeable and follow the instructions to obtain a claim number. Consumers will also be asked to destroy the product by writing in permanent marker “Recalled” and the claim number on the product, and to submit a photo showing the marked hand warmer, the product’s model number, and the four-digit batch number. Consumers should then dispose of the recalled product with the lithium-ion battery, in accordance with applicable local and state hazardous waste regulations. Note: Do not throw this recalled lithium-ion battery or device in the trash, the general recycling stream (e.g., street-level or curbside recycling bins), or used battery recycling boxes found at various retail and home improvement stores. Recalled lithium-ion batteries must be disposed of differently than other batteries, because they present a greater risk of fire. Your municipal household hazardous waste (HHW) collection center may accept this recalled lithium-ion battery or device for disposal. Before taking your battery or device to a HHW collection center, contact that office ahead of time and ask whether it accepts recalled lithium-ion batteries. If it does not, contact your municipality for further guidance.",
   "categories": [
    "electronics",
    "home"
   ],
   "agency_url": "https://www.cpsc.gov/Recalls/2027/Kobayashi-Recalls-Rechargeable-Hand-Warmers-Due-to-Risk-of-Serious-Injury-from-Fire-and-Burn-Hazards",
   "url": "https://consumersun.com/recall/cpsc-27011-rechargeable-hand-warmers"
  },
  {
   "agency": "CPSC",
   "recall_id": "27006",
   "date": "2026-10-01",
   "title": "LLK Trading Recalls Mochi Malrang Mystery Dumpling Toys Due to Risk of Serious Injury or Death from Water Bead Ingestion; Violate Mandatory Standard for Toys",
   "firm": "LLK Trading Inc., of Vernon, California",
   "product": "Mochi Malrang Mystery Dumpling Toys",
   "hazard": "The mystery dumpling toys violate the mandatory safety standard for toys because the water beads inside the dumplings expand larger than permitted, posing a deadly ingestion hazard. If a water bead is ingested, it can pose ingestion, choking, and intestinal obstruction hazards inside a child's body, resulting in severe discomfort, vomiting, dehydration and a risk of death to a child.",
   "remedy": "Consumers should stop using the mystery dumpling toys immediately and contact LLK Trading for a full refund. Consumers will be asked to write \"RECALLED\" in permanent marker on the squeezy dumpling and its tan plastic container, throw them away, and email a photo of the items in the trash to llktradinginc@gmail.com.",
   "categories": [
    "baby"
   ],
   "agency_url": "https://cpsc.gov/Recalls/2027/LLK-Trading-Recalls-Mochi-Malrang-Mystery-Dumpling-Toys-Due-to-Risk-of-Serious-Injury-or-Death-from-Water-Bead-Ingestion-Violate-Mandatory-Standard-for-Toys",
   "url": "https://consumersun.com/recall/cpsc-27006-mochi-malrang-mystery-dumpling-toys"
  },
  {
   "agency": "CPSC",
   "recall_id": "27010",
   "date": "2026-10-01",
   "title": "Walmart Recalls Over 4.4 Million Expert Grill Brushes Due to Ingestion Hazard",
   "firm": "Walmart, Inc. of Bentonville, Arkansas",
   "product": "Metal Wire Bristle Grill Brushes",
   "hazard": "Small metal wire bristles can detach from the brushes and stick to the grill or food, posing an ingestion hazard and risk of serious internal injuries that could require surgery.",
   "remedy": "Consumers should stop using the recalled grill brushes immediately and contact Walmart for a full refund or a credit for use at any Walmart store or Walmart.com. Consumers will be asked to return their recalled brushes to Walmart or discard them.",
   "categories": [
    "home"
   ],
   "agency_url": "https://www.cpsc.gov/Recalls/2027/Walmart-Recalls-Over-4-4-Million-Expert-Grill-Brushes-Due-to-Ingestion-Hazard",
   "url": "https://consumersun.com/recall/cpsc-27010-over-4-4-million-expert-grill-brushes"
  },
  {
   "agency": "CPSC",
   "recall_id": "27005",
   "date": "2026-10-01",
   "title": "YunHeng Recalls LandTale Bed Rails Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violate Mandatory Standard for Adult Portable Bed Rails",
   "firm": "Landtale Group Limited, dba YunHeng LLC, of China",
   "product": "LandTale Adult Portable Bed Rails",
   "hazard": "The recalled bed rails violate the mandatory standard for adult portable bed rails because users can become entrapped within the bed rail or between the bed rail and the side of the mattress, posing a serious entrapment hazard and risk of death by asphyxiation. In addition, the bed rails do not bear the required hazard warning labels.",
   "remedy": "Consumers should stop using the recalled adult portable bed rails immediately and contact YunHeng for a full refund. Consumers will be asked to destroy the bed rail by cutting off the handle's foam grip, disassembling the product and writing in permanent marker \"RECALLED\" on the upper and lower rails, and send a photo of the marked bed rails, showing the sender's name written on paper, to LandtaleBedRailsRecall@outlook.com. Consumers should then dispose of the destroyed product.",
   "categories": [
    "home"
   ],
   "agency_url": "https://www.cpsc.gov/Recalls/2027/YunHeng-Recalls-LandTale-Bed-Rails-Due-to-Risk-of-Serious-Injury-or-Death-from-Entrapment-and-Asphyxiation-Violate-Mandatory-Standard-for-Adult-Portable-Bed-Rails",
   "url": "https://consumersun.com/recall/cpsc-27005-landtale-bed-rails"
  },
  {
   "agency": "NHTSA",
   "recall_id": "26V635000",
   "date": "2026-10-01",
   "title": "Daimler Trucks North America, LLC: Insulation May Catch Fire",
   "firm": "Daimler Trucks North America, LLC",
   "product": "2025-2027 Freightliner Business Class M2 vehicles",
   "hazard": "Insulation that comes into contact with hot exhaust components increases the risk of a fire.",
   "remedy": "The remedy is currently under development. Owner notification letters are expected to be mailed November 30, 2026. Owners may contact DTNA customer service at 1-800-547-0712. DTNA's number for this recall is F1041.",
   "categories": [
    "vehicles"
   ],
   "agency_url": "https://www.nhtsa.gov/recalls?nhtsaId=26V635000",
   "url": "https://consumersun.com/recall/nhtsa-26v635000-daimler-trucks-north-america-llc-insulation-may"
  },
  {
   "agency": "NHTSA",
   "recall_id": "26V633000",
   "date": "2026-10-01",
   "title": "Honda (American Honda Motor Co.): Fuel Pump May Fail",
   "firm": "Honda (American Honda Motor Co.)",
   "product": "2023-2025 VT1300CX and 2024-2025 VT750 motorcycles",
   "hazard": "Fuel pump failure can cause an engine stall, increasing the risk of a crash.",
   "remedy": "Dealers will replace the fuel pump, free of charge. Owner notification letters will be mailed beginning November 27, 2026. Owners may contact Honda's customer service at 1-866-784-1870. Honda's number for this recall is KU9. Vehicle Identification Numbers (VINs) involved in this recall will be searchable on NHTSA.gov beginning October 8, 2026.",
   "categories": [
    "vehicles"
   ],
   "agency_url": "https://www.nhtsa.gov/recalls?nhtsaId=26V633000",
   "url": "https://consumersun.com/recall/nhtsa-26v633000-honda-american-honda-motor-co-fuel-pump-may-fail"
  },
  {
   "agency": "NHTSA",
   "recall_id": "26V632000",
   "date": "2026-10-01",
   "title": "Daimler Trucks North America, LLC: Insufficient Illumination from Low Beam Headlights",
   "firm": "Daimler Trucks North America, LLC",
   "product": "2027 Thomas Built SAF-T-LINER C2 and Thomas Built SAF-T-LINER C2 Jouley school buses",
   "hazard": "Insufficient low beam headlight illumination can reduce driver visibility, increasing the risk of a crash.",
   "remedy": "Dealers will inspect and replace the headlights, as necessary, free of charge. Owner notification letters are expected to be mailed November 30, 2026. Owners may contact DTNA customer service at 1-800-547-0712. DTNA's number for this recall is F1040.",
   "categories": [
    "vehicles"
   ],
   "agency_url": "https://www.nhtsa.gov/recalls?nhtsaId=26V632000",
   "url": "https://consumersun.com/recall/nhtsa-26v632000-daimler-trucks-north-america-llc-insufficient"
  },
  {
   "agency": "NHTSA",
   "recall_id": "26V631000",
   "date": "2026-10-01",
   "title": "Mack Trucks, Inc.: Intake and Grille Bezels May Detach",
   "firm": "Mack Trucks, Inc.",
   "product": "2026-2027 Anthem AN (4) and 2025-2027 Pioneer PR (4) vehicles",
   "hazard": "A detached bezel can become a road hazard for other vehicles, increasing the risk of a crash.",
   "remedy": "Dealers will inspect, replace the intake and grille bezels, and install cable ties as necessary, free of charge. Owner notification letters are expected to be mailed November 30, 2026. Owners may contact Mack's customer service at 1-800-866-1177. Mack's number for this recall is SC0501. Vehicle Identification Numbers (VINs) involved in this recall will become searchable on NHTSA.gov on October 8, 2026.",
   "categories": [
    "vehicles"
   ],
   "agency_url": "https://www.nhtsa.gov/recalls?nhtsaId=26V631000",
   "url": "https://consumersun.com/recall/nhtsa-26v631000-mack-trucks-inc-intake-and-grille-bezels-may"
  },
  {
   "agency": "FDA",
   "recall_id": "H-1395-2026",
   "date": "2026-09-30",
   "title": "WFM Purchasing, LP: Fromagerie Coop de Mean Cabricharme and Belgium Cabricharme Shelf life: 30 days recall",
   "firm": "WFM Purchasing, LP",
   "product": "Fromagerie Coop de Mean Cabricharme and Belgium Cabricharme Shelf life: 30 days, all dates through and including 10/7/2026 Packaging: Plastic wrapped by slice Net Wt.: Various, cut from whole wheel and priced by weight with Whole Foods Market scale label PLUs: 54670, 57953",
   "hazard": "Undeclared Egg Allergen",
   "remedy": null,
   "categories": [
    "food"
   ],
   "agency_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-1395-2026%22",
   "url": "https://consumersun.com/recall/fda-h-1395-2026-wfm-purchasing-lp-fromagerie-coop-de-mean"
  },
  {
   "agency": "FDA",
   "recall_id": "H-1396-2026",
   "date": "2026-09-30",
   "title": "GIAS FOOD INC.: Lemon Alfredo Fettuccine packed in a yellow plastic sealed bag with pink and black letteri recall",
   "firm": "GIAS FOOD INC.",
   "product": "Lemon Alfredo Fettuccine packed in a yellow plastic sealed bag with pink and black lettering; label reads in part as \"bettergoods Lemon Alfredo Fettuccine, MADE IN ITALY, NET WT 22 OZ, BEST if Used By: SEP 20 2027 L6080C, UPC 194346442706, DISTRIBUTED BY: Walmart Inc., Bentonville, AR 72716 PRODUCT OF ITALY",
   "hazard": "Contamination with Listeria monocytogenes",
   "remedy": null,
   "categories": [
    "food"
   ],
   "agency_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-1396-2026%22",
   "url": "https://consumersun.com/recall/fda-h-1396-2026-gias-food-inc-lemon-alfredo-fettuccine-packed-in"
  },
  {
   "agency": "FDA",
   "recall_id": "H-1393-2026",
   "date": "2026-09-30",
   "title": "Kwok Shing, Inc.: American Ginsengs recall",
   "firm": "Kwok Shing, Inc.",
   "product": "American Ginsengs. PRODUCT OF WISCONSIN. NET WT: 4 oz. NET WT. 8 oz.",
   "hazard": "Potential contamination with pesticides.",
   "remedy": null,
   "categories": [
    "food"
   ],
   "agency_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-1393-2026%22",
   "url": "https://consumersun.com/recall/fda-h-1393-2026-kwok-shing-inc-american-ginsengs"
  },
  {
   "agency": "FDA",
   "recall_id": "H-1391-2026",
   "date": "2026-09-30",
   "title": "United Sugar Producers and Refiners: Light Brown Sugar recall",
   "firm": "United Sugar Producers and Refiners",
   "product": "Light Brown Sugar, Packaged in he follow configurations: 1. United, Net Wt. 50 lbs., (22.68kg). Item Number 810051. Distributed By: United Sugar Producers & Refiners, Minneapolis, MN 55439. 2. Good & Gather, Net Wt 2 lb. (32 oz) 907g. Item Number 817773. UPC 0 85239-08454 0. Dist. By Target Corp., Minneapolis, MN 55403.",
   "hazard": "Potential Wheat Kernel contamination.",
   "remedy": null,
   "categories": [
    "food"
   ],
   "agency_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-1391-2026%22",
   "url": "https://consumersun.com/recall/fda-h-1391-2026-united-sugar-producers-and-refiners-light-brown"
  },
  {
   "agency": "FDA",
   "recall_id": "H-1392-2026",
   "date": "2026-09-30",
   "title": "United Sugar Producers and Refiners: Powdered Sugar recall",
   "firm": "United Sugar Producers and Refiners",
   "product": "Powdered Sugar, Packaged in the following configurations: 1. United 6X, Net Wt. 50 lbs. (22.68kg), Item Number 810087. UPC 7 85921-07090 4. Distributed by: United Sugar Producers & Refiners, Minneapolis, MN 55439. 2. Crystal Sugar, Net Wt. 25 lbs. (11.3 kg), Item Number 810097. UPC 0 70090-08090 9. Distributed by Crystal Sugars Corporation, Moorhead, MN 2. Good & Gather, Net Wt 2 lb. (32oz) 907g. Item Number 817774. UPC 0 85239-08455 7. Dist. By Target Corp. Minneapolis, MN 55403.",
   "hazard": "Potential Wheat Kernel contamination.",
   "remedy": null,
   "categories": [
    "food"
   ],
   "agency_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-1392-2026%22",
   "url": "https://consumersun.com/recall/fda-h-1392-2026-united-sugar-producers-and-refiners-powdered-sugar"
  },
  {
   "agency": "FDA",
   "recall_id": "H-1394-2026",
   "date": "2026-09-30",
   "title": "WWF Operating Company: So Delicious Dairy Free Salted Caramel Cluster Cashewmilk recall",
   "firm": "WWF Operating Company",
   "product": "So Delicious Dairy Free Salted Caramel Cluster Cashewmilk, Non-Dairy Frozen Dessert. 16 oz paper tub with an attached paper lid. Sold as a single unit multi serving tub. UPC 744473 476138. Distributed by For So Delicious Dairy Free Eugene, OR 97402.",
   "hazard": "Product may contain foreign material: small stones and other hard objects.",
   "remedy": null,
   "categories": [
    "food"
   ],
   "agency_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-1394-2026%22",
   "url": "https://consumersun.com/recall/fda-h-1394-2026-wwf-operating-company-so-delicious-dairy-free"
  }
 ]
}