Conmed Corporation: Insufflator, Laparoscopic
ConMed Insufflator Recall Summary ConMed Corporation is recalling AirSeal 5mm Access Ports and related laparoscopic surgical equipment (model iAS5-120LP) distributed nationwide because the carbon dioxide insufflator may fail to properly alert when pressure reaches unsafe levels. This is a Class II recall affecting surgical facilities that received these disposable trocar and cannula devices.
- Recalling firm
- ConMed Corporation
- Product
- ConMed AirSeal 5mm Access Port and Low Profile Obturator with Bladeless Optical Tip, 120mm Length. Catalog Number: iAS5-120LP. 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/af311346-4882-4418-be6d-cb15dcd8dc49