medical MODERATE Updated 2026-06-24

ConMed Corporation recalls ConMed AirSeal 12mm Access Port and Palm Grip Obturator with

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Recalled Product

ConMed AirSeal 12mm Access Port and Palm Grip Obturator with Bladeless Optical Tip, 100mm Length. Catalog Number: iAS12-100LPI. 6 units per pack. Disposable Endoscopic Trocar and Cannula; Carbon Dioxide Insufflator for Laparoscopy.

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Hazard / Issue

Potential for overpressure alerts.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: Catalog Number: iAS12-100LPI. UDI-DI: 10845854045640. Lot Numbers: 2025082210, 202502265, 202601074, 202512034, 202601084, 202512194, 202512184, 202512204, 202512224, 202512024, 2026010610, 2025100710, 202512094, 202512174, 2025121810, 202510214, 2026010511, 202510024, 202510104, 202510224, 202510084, 2025121710, 202510064, 202512104, 202512164, 202512064, 202512084, 202512054, 202512044, 202512154, 202510014, 202511144, 202511254, 202511264, 202510074, 202510144, 202511124, 202509094, 202509194, 202509294, 2025093010, 202509304, 202511134, 202511194, 202509084, 2025102310, 202510294, 202510304, 202510314, 202511046, 202511114, 2025101510, 202511154, 202511184, 202509184, 202510284, 202509174, 202511014, 202511044, 202511054, 202509044, 202509164, 202510274, 2025082210, 2025101310, 202509224, 2025092910, 202510134, 2025100610, 202508194, 202508234, 202509054, 202508184, 2025082110, 202508224, 202508144, 2025082010, 2025081110, 202508114, 202508134, 202508154, 202508054, 202508074, 2025080610, 202508254, 202507304, 202508064, 202507214, 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202409194, 2025051310, 202511034, 202410155, 202409036, 202407316, 202505236, 202502215, 202407184, 202409304, 2024120411, 2024120311, 202408016, 202409195, 202412036, 2025081210, 202407035, 202408055, 2024121811, 202407195, 202501186, , 202410085, 202504294, 202502115, 202410224, 2024120410, 202509034, 202412056, 2024072510, 202409124, 202410025, 202407305, 202501096, 202411124, 202410154, 202407036, 202410024, 202407096, 202411185, 202407246, 202408086, 202407196, 202406275, 2026010710, 2024111510, 202412164, 202412035, 202407056, 202411155. *OUS added 06/10/2026 expansion: 202412165, 2024121611, 2024110810, 202512164, 202512174, 202509174, 202510284, 202509304, 202508074, 202508194, 202508184, 202507304, 202506204, 2025062010, 202506174, 202506054, 2025060510, 202507174, 202507184, 202503296, 202503314, 2025042910, 202505074, 2025061010, 202506074, 202412026, 202411306, 202411284, 202503035, 202502245, 202412044, 202502284, 202410144, 202410114, 202408306, 202411114, 2024121710, 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2025052710, 202502285, 2024121410, 202501175, 202410175, 202410084, 202409175, 202406156, 202503276, 202512094, 202509084, 202411065, 202512034, 202510214, 202511014, 202510314, 202411115, 202411285, 202407084, 202411286, 202512084, 202511194, 202503265, 202412196, 202502145, 202409204, 202511114, 202507224, 202508114, 2025070210, 202506184, 2025060410, 202506034, 202506044, 202503055, 202501306, 202411064, 202410094, 202407045, 202406196, 202407315, 202407066, 202409114, 202510064, 202509184, 202510074, 2025060910, 202510224, 2025082110, 202504116, 202505274, 202502016, 202410025, 202502274, 202412174, 2025101510, 2025100710, 202512204, 202511254, 202503145, 202412184, 202407096, 202406264, 202409174, 202504144, 202412164, 202502254, 202412186, 202507154, 202505124, 202501065, 202408215, 202412146, 202504095, 202506194, 2024121011, 202410155, 202409194, 202409185, 202409184, 202407054, 2025082210, 202507284, 2025072510, 2025072410, 202503045, 202511264, 202510104, 202512184, 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Manufactured from 14 June 2024 to 12 January 2026.

✅ What Should You Do?

  1. 1Contact your healthcare provider immediately to discuss this recall.
  2. 2Stop using the device if it is safe to do so, and contact your provider.
  3. 3Follow the manufacturer's remedy instructions provided in the recall notice.
  4. 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.

Looking for a safe alternative?

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