Medline Industries, LP recalls Convenience Kits containing CONMED AirSeal Access Ports ADVANCE LAPAROSCOPIC DYNJ911
- Recalling company
- Medline Industries, LP
- Product
- Convenience Kits containing CONMED AirSeal Access Ports ADVANCE LAPAROSCOPIC DYNJ911135 LAP CHOLE DYNJ911660 LAP NISSEN DYNJ911560 UROLOGY LAPAROSCOPIC - 51638 DYNJ908720A
- 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
- DYNJ911135 UDI-DI 10198459264382 Lots 25EDA279 25FDB612 25LDB658 DYNJ911660 UDI-DI 10198459487071 Lots 25IMF444 25JMA458 26BMG519 26DMA914 26EMA779 26FME775 26GMA849 26GMF826 26GMM101 26GMM127 DYNJ911560 UDI-DI 10198459400261 Lots 25HMG749 25JMC886 25KMA383 25KMA392 DYNJ908720A UDI-DI 10195327423155 Lots 24DBN292 24GBJ114 24IBK504 24JBC471 25KBP733 26ABG732
- Company location
- Northfield, IL
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-0180-2027
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-0180-2027 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.