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Home › FDA recalls › Convenience Kits containing CONMED AirSeal Access Ports A
CLASS II · ModerateFDA

Medline Industries, LP recalls Convenience Kits containing CONMED AirSeal Access Ports ADVANCE LAPAROSCOPIC DYNJ911

📅 Aug 31, 2026 · 📍 Nationwide
Recalling company
Medline Industries, LP
Product
Convenience Kits containing CONMED AirSeal Access Ports ADVANCE LAPAROSCOPIC DYNJ911135A CHN GYN ONCOLOGY DYNJ906731M
Reason
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.
Classification
Class II – may cause temporary or medically reversible health consequences
Recall date
Aug 31, 2026
Reported
Oct 21, 2026
Distribution
US Nationwide distribution in the states of AZ, CA, IN, MD, MO, NJ, OH, and WI.
Status
Ongoing
Quantity
3,551 kits
Lot / codes
DYNJ911135A UDI-DI 10198459655623 Lot 26EDA606 DYNJ906731M UDI-DI 10198459567117 Lots 25KDA658 25KDB571 25LDB411 26CDA536
Company location
Northfield, IL
Recall type
Voluntary: Firm initiated
Recall number
Z-0184-2027
Agency
U.S. Food and Drug Administration (FDA)

View official FDA notice ↗ Search recall number Z-0184-2027 in the FDA Enforcement Report. Also see FDA recall press releases.

If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.