Home / Recalls / ConMed Corporation / Z-2472-2026

Z-2472-2026 Class II Ongoing

Recalled by ConMed Corporation — Utica, NY

FDA device recall Z-2472-2026 was initiated by ConMed Corporation on May 14, 2026 and is designated Class II. Reason for recall: Potential for overpressure alerts. The recall status is ongoing. Affected quantity: 3,550 packs (21,300 eaches).

Recall Details

Product Type
Devices
Report Date
June 24, 2026
Initiation Date
May 14, 2026
Termination Date
N/A
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
3,550 packs (21,300 eaches)

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.

Distribution Pattern

Nationwide distribution. International distribution to Australia, Austria, Belgium, Bosnia and Herzegovina, Canada, CHILE, CHINA, COLOMBIA, Croatia, Denmark, DOMINICAN REPUBLIC, ECUADOR, Egypt, Estonia, Finland, France, Germany, Greece, HONG KONG, India, INDONESIA, Iraq, Ireland, Israel, Italy, Japan, Jordan, Kuwait, Lebanon, Libya, Luxembourg, MALAYSIA, Malta, Montenegro, Netherlands, NEW ZEALAND, Norway, Oman, Palestine, PANAMA, PHILIPPINES, Poland, Qatar, Romania, Russia, Saudi Arabia, Serbia, SINGAPORE, Slovakia, South Africa, South Korea, Spain, Sweden, Switzerland, TAIWAN,PROVINCE OF CHINA, THAILAND, Turkey, Ukraine, UNITED ARAB EMIRATES, United Kingdom. .

Code Information

Catalog Number: iAS12-150LPI. UDI-DI: 10845854052006. Lot Numbers: 202509234, 202506104, 202505074, 202503204, 202510094, 202510144, 202508194, 202506244, 202512054, 202512234, 202511224, 202504164, 202504074, 202407294, 202511214, 202410254, 202512184, 202412175, 202407115, 202411055, 202411284, 202408235, 202411274, 202502275. *OUS added 06/10/2026 expansion: 202510144, 202510094, 202506244, 202509234, 202504074, 202412175, 202408235, 202407294, 202508194, 202410254, 202408234, 202503204, 202506104, 202411055, 202505074, 202504164, 202512184, 202411274, 202511224, 202511214, 202601124, 202502275, 202411284, 202512054, 202407115. Manufactured from 14 June 2024 to 12 January 2026.

Other recalls by ConMed Corporation

  • Z-2466-2026 Class II — ConMed AirSeal 12mm Access Port and Obturator with Blunt Tip, 100mm Length. Cata (May 14, 2026)
  • Z-2468-2026 Class II — ConMed AirSeal 8mm Access Port and Low Profile Obturator with Bladeless Optical (May 14, 2026)
  • Z-2470-2026 Class II — ConMed AirSeal 5mm Access Port and Low Profile Obturator with Bladeless Optical (May 14, 2026)
  • Z-2474-2026 Class II — ConMed AirSeal 12mm Access Port and Palm Grip Obturator with Bladeless Optical T (May 14, 2026)
  • Z-2465-2026 Class II — ConMed AirSeal 12 mm Access Port and Obturator with Blunt Tip, 120mm Length. Cat (May 14, 2026)
  • Z-2467-2026 Class II — ConMed AirSeal 8mm Access Port and Low Profile Obturator with Bladeless Optical (May 14, 2026)
  • Z-2473-2026 Class II — ConMed AirSeal 12mm Access Port and Low Profile Obturator with Bladeless Optical (May 14, 2026)
  • Z-2464-2026 Class II — ConMed AirSeal 5 mm Smooth Access Port and Obturator with Blunt Tip, 150mm Lengt (May 14, 2026)
  • Z-2471-2026 Class II — ConMed AirSeal 5mm Access Port and Low Profile Obturator with Bladeless Optical (May 14, 2026)
  • Z-2469-2026 Class II — ConMed AirSeal 5mm Access Port and Low Profile Obturator with Bladeless Optical (May 14, 2026)

FDA data resources