Conmed Corporation: Insufflator, Laparoscopic
ConMed Insufflator Recall Summary ConMed Corporation is recalling the AirSeal 5mm Access Port and Low Profile Obturator (catalog number iAS5-75LP), which are surgical devices used in laparoscopic procedures. The devices have a potential defect that could cause overpressure alerts to occur. The recall affects units distributed nationwide across all U.S. states and Washington, D.C.
- Recalling firm
- ConMed Corporation
- Product
- ConMed AirSeal 5mm Access Port and Low Profile Obturator with Bladeless Optical Tip, 75mm Length. Catalog Number: iAS5-75LP. 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/2405c0b5-8938-4d4b-97be-e95fe3f17b23