Conmed Corporation: Insufflator, Laparoscopic
ConMed Corporation is recalling its AirSeal 12 mm Access Port and Obturator with Blunt Tip (Catalog Number iASB12-120) used in laparoscopic surgery because the device may not properly alert when pressure becomes too high during the procedure. The recall affects units distributed nationwide across all U.S. states and Washington, D.C.
- Recalling firm
- ConMed Corporation
- Product
- ConMed AirSeal 12 mm Access Port and Obturator with Blunt Tip, 120mm Length. Catalog Number: iASB12-120. 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/3258d7e1-ca23-4c80-962f-dda31b761461