FDAFDA · Food and drugs·Recall number Z-2472-2026
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.
Published June 24, 2026 · Recall initiated: May 14, 2026
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Potential for overpressure alerts.
What to do
Voluntary: Firm initiated · Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Recall details
- Manufacturer
- ConMed Corporation
- Distributor
- 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. .
- Lot
- 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.
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
Sell products like this?
Recalert watches your whole catalog for recalls like this one, automatically.