Conmed Corporation: Insufflator, Laparoscopic
ConMed Insufflator Recall Summary ConMed Corporation is recalling its AirSeal 12mm Access Port and Palm Grip Obturator (catalog number iAS12-100LPI), which are surgical devices used in laparoscopic procedures, because they may not properly alert when pressure becomes too high. The recalled units were distributed nationwide across all 50 states, Washington D.C., and U.S. territories.
- Recalling firm
- ConMed Corporation
- Product
- ConMed AirSeal 12mm Access Port and Palm Grip Obturator with Bladeless Optical Tip, 100mm Length. Catalog Number: iAS12-100LPI. 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/abcb46d9-32f3-437f-ac0d-77a44c80e0c7