Medline Industries, Lp: Laparoscopy Kit
Medline Industries is recalling laparoscopy convenience kits (used in surgical procedures) because they contain CONMED AirSeal Access Ports that may malfunction and trigger false pressure alerts or leak air during surgery, potentially interrupting or ending procedures. The recall affects four kit models distributed nationwide, though primary distribution was in Arizona, California, Indiana, Maryland, Missouri, New Jersey, Ohio, and Wisconsin. This is a Class II recall, meaning the defect could cause serious problems but is unlikely to result in death or permanent injury.
- Recalling firm
- 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
- Category
- medical device recall
- Country
- United States
- Agency
- FDA-DEVICES
- Recall date
- 2026-08-31
- Status
- Open, Classified
- Areas affected
- AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
- Distribution
- US Nationwide distribution in the states of AZ, CA, IN, MD, MO, NJ, OH, and WI.
Official recall notice from FDA-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/8f6c9faa-692a-443c-9679-c4c6f244e4c0