ConMed AirSeal 8mm Access Port and Low Profile Obturator with Bladeless Optical Tip recall (ConMed Corporation)
Medical deviceClass IIOngoing
Summary: ConMed Corporation is recalling ConMed AirSeal 8mm Access Port and Low Profile Obturator with Bladeless Optical Tip, 100mm Length. Catalog Number: iAS8-100LP. 6 units per pack. Disposable Endoscopic Trocar and Cannula; Carbon Dioxide Insufflator for Laparoscopy.. Reason: Potential for overpressure alerts.
What is being recalled
ConMed AirSeal 8mm Access Port and Low Profile Obturator with Bladeless Optical Tip, 100mm Length. Catalog Number: iAS8-100LP. 6 units per pack. Disposable Endoscopic Trocar and Cannula; Carbon Dioxide Insufflator for Laparoscopy.
Why
Potential for overpressure alerts.
How serious is it
Class II is the middle level: using or being exposed to this product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
Where it was sold
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. .
How to tell if yours is affected
Catalog Number: iAS8-100LP. UDI-DI: 10845854045718. Lot Numbers: 202509034, 202511194, 202509174, 202506264, 202506254, 202506274, 202507074, 202505096, 202507244, 202508124, 202508194, 202507084, 202504294, 202505074, 202504304, 202504155, 202505064, 202505094, 202505204, 202509244, 202511184, 2025102210, 202508254, 2025111110, 202510154, 202508054, 202508114, 202507254, 202509084, 202509054, 202411015, 202408155, 202503016, 202504234, 202505264, 202501134, 202411124, 202501135, 202412195, 202411305, 202511274, 202509274, 202511284, 202504284, 202504224, 202503194, 202504085, 202508184, 202510304, 202409034, 202409095, 202409094, 202408085, 202410104, 202506304, 202506054, 202510094, 202409025, 202410175, 202508264, 202408095, 202408125, 202411115, 202411014, 202506044, 202509194, 202511264, 202408274, 202412205, 202412025, 202501236, 202501235, 202501244, 202503156, 202503145, 202503144, 202504084, 202408094, 202408084, 202410105, 202502066, 202501094, 202509184, 202408275, 202408194, 202507144, 202507154, 202412024, 202501234, 202411295, 202504094, 202503196, 202503125, 202503126, 202503034, 202504145, 202408165, 2025081811, 202408154, 202503264, 202502055, 202411294, 202412106, 202601074, 2026010711, 202501225, 202412204, 202501245, 202409106, 202410315. *OUS added 06/10/2026 expansion:202408284, 202509244, 202507254, 202508054, 202508194, 202505064, 202504294, 202504155, 202504304, 202501085, 202501146, 202501274, 202501224, 202410314, 202410315, 202509034, 2025111110, 202509174, 202507244, 202508124, 202506274, 202505204, 202506254, 202503144, 202409106, 202511184, 202505096, 202501225, 202510154, 202408165, 202508114, 202508254, 202408085, 202507084, 202505094, 202507074, 202503194, 202501135, 202412205, 202412204, 202408084, 202411295, 202412106, 202509054, 202509084, 2025102210, 202504084, 202503196, 202504145, 202501094, 202408164, 202411124, 202503125, 202408094, 202505074, 202504224, 202411294, 202507144, 202408095, 202506304, 202511274, 202508184, 202503264, 202411115, 202504234, 202506264, 202501244, 202503034, 202509184, 202501236, 202411305, 202510304, 202505264, 202502055, 202412025, 202412195, 202410175, 202506054, 2025081811, 202503016, 202409034, 202409094, 202501134, 202507154, 202511284, 202506044, 202510094, 202411015, 202503145, 202408274, 202511264, 202411014, 202408155, 202509274, 202503156, 202508264, 202408194, 202504094, 202501234, 202408275, 202408154, 202408075, 202511194, 202504085, 202501245, 202412024, 202410115, 202412126, 202409025, 202409095, 202501235, 202410104. Manufactured from 14 June 2024 to 12 January 2026.
What to do
Check the model, lot or serial numbers above against your device. If yours is affected, contact the manufacturer or your healthcare provider before you stop using a device you rely on.
Recall facts
| Recall number | Z-2468-2026 |
| Category | Medical device |
| Agency | U.S. Food and Drug Administration (FDA) |
| Severity | Class II |
| Status | Ongoing |
| Recall started | May 14, 2026 |
| Reported | June 24, 2026 |
| Company | ConMed Corporation |
| Company location | Utica, NY, United States |
| Initiated by | Voluntary: Firm initiated |
| Quantity | 26,609 packs (159,657 eaches) |
More recalls from ConMed Corporation · all medical device recalls · recalls from May 2026