Conmed Corporation: Insufflator, Laparoscopic
ConMed Insufflator Recall Summary ConMed Corporation is recalling the AirSeal 12mm Access Port and Obturator with Blunt Tip (Catalog Number iASB12-100) because the carbon dioxide insufflator used in laparoscopic surgery may fail to generate proper overpressure alerts. The recalled product was distributed nationwide to all U.S. states and Washington D.C. This is a Class II recall affecting medical facilities and surgical centers that use this equipment.
- Recalling firm
- ConMed Corporation
- Product
- ConMed AirSeal 12mm Access Port and Obturator with Blunt Tip, 100mm Length. Catalog Number: iASB12-100. 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/80a05a6b-f422-4f6c-95da-58dd9359f9ff