Conmed Corporation: Insufflator, Laparoscopic
ConMed Insufflator Recall Summary ConMed Corporation is recalling the AirSeal 5mm Access Port and Low Profile Obturator (catalog number iAS5-100LP), surgical devices used in laparoscopic procedures, because they may fail to provide proper overpressure alerts. The devices were distributed nationwide across all U.S. states and the District of Columbia. This is classified as a Class II recall, indicating a potential health hazard.
- Recalling firm
- ConMed Corporation
- Product
- ConMed AirSeal 5mm Access Port and Low Profile Obturator with Bladeless Optical Tip, 100mm Length. Catalog Number: iAS5-100LP. 6 units per pack. Disposable Endoscopic Trocar and Cannula; Carbon Dioxide Insufflator for Laparoscopy.
- Reason
- Potential for overpressure alerts.
- Classification
- Class II
- Category
- medical device recall
- Country
- United States
- Agency
- FDA-DEVICES
- Recall date
- 2026-05-14
- Status
- Open, Classified
- Areas affected
- AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
- Distribution
- Nationwide distribution
Official recall notice from FDA-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/b7995e99-136a-4c96-b624-290b594f1aba