Recall Z-2465-2026— ConMed Corporation

Name: FDA recall Z-2465-2026
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 12 mm Access Port and Obturator with Blunt Tip, 120mm Length. Catalog Number: iASB12-120. 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 12 mm Access Port and Obturator with Blunt Tip, 120mm Length. Catalog Number: iASB12-120. 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.