ConMed Corporation recalls ConMed AirSeal 5mm Access Port and Low Profile Obturator with Bladeless Optical Tip

Recalling company

ConMed Corporation

Product

ConMed AirSeal 5mm Access Port and Low Profile Obturator with Bladeless Optical Tip, 100mm Length. Catalog Number: iAS5-100LP. 6 units per pack. Disposable Endoscopic Trocar and Cannula; Carbon Dioxide Insufflator for Laparoscopy.

Reason

Potential for overpressure alerts.

Classification

Class II – may cause temporary or medically reversible health consequences

Recall date

May 14, 2026

Reported

Jun 24, 2026

Distribution

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. .

Status

Ongoing

Quantity

36,462 packs (219,850 eaches)

Lot / codes

Catalog Number: iAS5-100LP. UDI-DI: 10845854045626. Lot Numbers: 202509104, 202502195, 202502255, 202503115, 202503205, 202504084, 202503114, 202503035, 202503204, 202510214, 202511044, 202511055, 202510144, 202510284, 202510134, 202511184, 202510294, 202510224, 202511066, 202511124, 202511144, 202511154, 202505284, 202506064, 202506204, 202507014, 202504074, 202507154, 202507294, 202507164, 202507284, 202506194, 202507024, 202505194, 202504014, 202503215, 202505274, 202511134, 202509154, 202509294, 202508274, 202509234, 202510014, 202508044, 202508134, 202508154, 202509114, 202411224, 202509224, 202506216, 202410074, 202410155, 202410154, 202410224, 202412045, 202501064, 202509024, 202503116, 202504024, 202503124, 202502274, 202502175, 202411205, 202407094, 202503206, 202502264, 202408224, 202409105, 202411264, 202506074, 202412164, 202509304, 202601124, 202502184, 202512024, 202502194, 202506094, 202509014, 202508264, 202509124, 202506184, 202506234, 202507074, 202508014, 202508184, 202411255, 202411204, 202510074, 202408305, 202406215, 202501296, 202410025, 202406205, 202411214, 202410284, 202409245, 202410164, 202409186, 202407194, 202410084, 202412134, 202409246, 202502114, 202502054, 202502045, 202411254, 202409244, 202502116, 202407254, 202406285, 202502105, 202412035, 202406214, 202408135, 202502265, 202511114, 202409235, 202509244, 202408064, 202503214, 202503046, 202507214, 202512014, 202409286, 202502276, 202501035, 202501036, 202504164, 202503055, 202507034, 20240

Company location

Utica, NY

Recall type

Voluntary: Firm initiated

Recall number

Z-2471-2026

Agency

U.S. Food and Drug Administration (FDA)

View official FDA notice ↗ Search recall number Z-2471-2026 in the FDA Enforcement Report. Also see FDA recall press releases.