Conmed Corporation: Insufflator, Laparoscopic
Recall Summary ConMed Corporation is recalling its AirSeal 5 mm Smooth Access Port and Obturator (Catalog Number iASB5-150), a disposable surgical device used in laparoscopic procedures, because it may not properly alert medical staff when pressure levels become too high during surgery. The product was distributed nationwide across all U.S. states and the District of Columbia.
- Recalling firm
- ConMed Corporation
- Product
- ConMed AirSeal 5 mm Smooth Access Port and Obturator with Blunt Tip, 150mm Length. Catalog Number: iASB5-150. 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/7da11caa-35f7-45c3-ae34-e3f677607a0d