Conmed Corporation: Insufflator, Laparoscopic
ConMed Corporation is recalling certain laparoscopic insufflator devices (catalog number iAS12-120LPI) used in surgical procedures because they may fail to properly alert medical staff when pressure levels become too high. The recall affects units distributed nationwide across all U.S. states and Washington, D.C.
- Recalling firm
- ConMed Corporation
- Product
- ConMed AirSeal 12mm Access Port and Low Profile Obturator with Bladeless Optical Tip, 120mm Length. Catalog Number: iAS12-120LPI. 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/e44eb592-2e00-45ec-afa6-7e380da92fd5