Recall Z-2472-2026— ConMed Corporation

Name: FDA recall Z-2472-2026
Creator: U.S. Food and Drug Administration
Published: 2026-05-14

Class II · Ongoing

Class II FDA medical device recall by ConMed Corporation, initiated 2026-05-14. It names one FDA 510(k) clearance: K143404. Product: ConMed AirSeal 12mm Access Port and Palm Grip Obturator with Bladeless Optical Tip, 150mm Length. Catalog Number: iAS12-150LPI. 6 units per pack. Disposable Endoscopic Trocar and Cannula; Carbon Dioxide Insufflator for Laparoscopy.. Reason: Potential for overpressure alerts..

Recalling firm: ConMed Corporation
Classification: Class II
Status: Ongoing
Initiated: 2026-05-14
Firm location: Utica, NY, United States

510(k) clearances named in this recall

1 on FDA's record

K143404 — SurgiQuest AirSeal iFS SystemSurgiquest, Inc.·cleared 2015-03-20

K-numbers as listed on FDA's Recall Enterprise System record for this event (openFDA device/recall k_numbers). The recall may also cover devices cleared under other submissions not named here.

Product description

ConMed AirSeal 12mm Access Port and Palm Grip Obturator with Bladeless Optical Tip, 150mm Length. Catalog Number: iAS12-150LPI. 6 units per pack. Disposable Endoscopic Trocar and Cannula; Carbon Dioxide Insufflator for Laparoscopy.

Reason for recall

Potential for overpressure alerts.

Data sourced from openFDA. This site is unofficial and independent of the FDA.