FDAFDA recall Z-2837-2026 · Aug 12, 2026
INTEGRATED MEDCRAFT LLC: Kingfisher Compact Individual First Aid Kit recall
Recall found
Product
Kingfisher Compact Individual First Aid Kit. REF Number: 76656. Containing the affected One-piece Guedel airway components: 1. Size 00, ISO 5.0, blue. Product Code: 1100050. 2. Size 000, ISO 3.5, light green. Product Code: 1000035.
Reason for recall
Devices could potentially contain an occluded or partially occluded Guedel Airway tip.
What to do
FDA enforcement reports don't include consumer instructions. Check the codes below against your packaging. If this is a medicine or device you use, talk to your pharmacist or doctor before you stop or change anything, and contact the company or FDA for what to do with the product.
Recall details
- FDA classification
- Class II: use of or exposure to the product may cause temporary or medically reversible health problems, or the chance of serious problems is remote.
- Status
- Ongoing
- Codes, lots and dates
- Kingfisher Compact Individual First Aid Kit. REF Number: 76656. Lot Numbers: IMC-00000132, IMC-00000139. Containing the affected One-piece Guedel airway components 1. Size 00, ISO 5.0, blue. Product Code: 1100050. Lot Numbers: 32121232, 32208193, 32400267, 32403734, 32408819, 32409672, 32416545, 32427064, 32605471, 32606405, 32606850, 32607154. 2. Size 000, ISO 3.5, light green. Product Code: 1000035. Lot Numbers: 32190425, 32213076, 32221283, 32307261, 32317627, 32321305, 32513841, 32517565
- Distribution
- US Nationwide distribution.
- Recalling firm
- INTEGRATED MEDCRAFT LLC, East Hampton, CT
- Voluntary or mandated
- Voluntary: Firm initiated
- Recall started
- 2026-07-07
Source: openFDA enforcement record Z-2837-2026 · search recall number Z-2837-2026 in FDA's Enforcement Report.
Copied from the agency record without changes. Data as of Oct 22, 2026, 4:56 AM EDT. The agency notice is the final word.