Conmed Corporation: Insufflator, Laparoscopic
Recall Summary ConMed Corporation is recalling its AirSeal 8mm Access Port and related laparoscopic surgical equipment nationwide due to potential overpressure alerts that may not function correctly. The recalled devices are used during minimally invasive abdominal surgeries to maintain pressure in the surgical area. This is a Class II recall affecting healthcare facilities across all 50 states and Washington, D.C.
- Recalling firm
- ConMed Corporation
- Product
- ConMed AirSeal 8mm Access Port and Low Profile Obturator with Bladeless Optical Tip, 120mm Length. Catalog Number: iAS8-120LP. 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/7fe90849-7a06-4cbd-bcd3-3d5b19c1a322