FDAFDA recall Z-0182-2027 · Oct 21, 2026
Medline Industries, LP: Convenience Kits containing CONMED AirSeal Access Ports GENERAL DAVINCI DYNJG901004C LAP C recall
Recall found
Product
Convenience Kits containing CONMED AirSeal Access Ports GENERAL DAVINCI DYNJG901004C LAP CHOLE DYNJ88071 ROBOTIC PACK DYNJ50474F
Reason for recall
Kits contain CONMED AirSeal Access Ports. The ports were recalled by manufacturer due to potential for erroneous overpressure alerts and system venting during use, which may result in delays or ending procedures.
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
- DYNJG901004C UDI-DI 10198459535772 Lots 25LLA307 26BLA900 DYNJ88071 UDI-DI 10198459098512 Lots 24KMD416 24LMG268 25AMH987 25BMA076 25GMK411 DYNJ50474F UDI-DI 10195327559007 Lots 24DDA107 24DDA469 24EDA512 24GDB884 24IDA882
- Quantity
- 3,551 kits
- Distribution
- US Nationwide distribution in the states of AZ, CA, IN, MD, MO, NJ, OH, and WI.
- Recalling firm
- Medline Industries, LP, Northfield, IL
- Voluntary or mandated
- Voluntary: Firm initiated
- Recall started
- 2026-08-31
Source: openFDA enforcement record Z-0182-2027 · search recall number Z-0182-2027 in FDA's Enforcement Report.
Copied from the agency record without changes. Data as of Oct 26, 2026, 8:14 PM EDT. The agency notice is the final word.