Class 2 Device Recall ConMed AirSeal 5mm Access Port and Low Profile Obturator with Bladeless Optical Tip

• Date Initiated by Firm: May 14, 2026
• Date Posted: June 17, 2026
• Recall Status: Open, Classified
• Recall Number: Z-2470-2026
• Recall Event ID: 98854
• 510(K)Number: K143404
• Product Classification: Insufflator, laparoscopic - Product Code HIF
• Product: ConMed AirSeal 5mm Access Port and Low Profile Obturator with Bladeless Optical Tip, 120mm Length. Catalog Number: iAS5-120LP. 6 units per pack. Disposable Endoscopic Trocar and Cannula; Carbon Dioxide Insufflator for Laparoscopy.
• Code Information: Catalog Number: iAS5-120LP. UDI-DI: 10845854045657. Lot Numbers: 202504214, 202511075, 202510254, 202510274, 202510244, 202511104, 202601084, 202506054, 202506114, 202506104, 202505164, 202505294, 202505154, 202505176, 202507174, 202507184, 202507214, 202507044, 202506244, 202507024, 202507034, 202510024, 202510104, 202509194, 202507314, 202508134, 202508144, 202509224, 202509164, 202508294, 202509084, 202507315, 202507294, 202410094, 202410254, 202411114, 202409254, 202409255, 202505014, 202504224, 202502174, 202502254, 202504034, 202408234, 202501145, 202412124, 202408305, 202511064, 202510234, 202409114, 202409126, 202410174, 202510084, 202407105, 202502115, 202411194, 202508154, 202502134, 202502145, 202501174, 202510074, 202509094, 202505054, 202508014, 202506094, 202506174, 202506164, 202511065, 202601094, 202406245, 202409146, 202501316, 202502044, 202501154, 202502016, 202501155, 202501024, 202502245, 202503245, 202503266, 202503244, 202504044, 202504046, 202504164, 202407195, 202408235, 202407104, 202407224, 202410244, 202411074, 202412054, 202508274, 202501304, 202501144, 202504025, 202502135, 202501315, 202501295, 202504304, 202408225, 202409115, 202502045, 202504305, 202509014, 202509154, 202410165, 202408054, 202412174, 202412055, 202502126, 202501035, 202409135, 202507304, 202508284, 202409124, 202501305, 202410075, 202409125, 202502244, 202412165, 202501025, 202502156, 202511076, 202411075, 202510014, 202408024, 202412064, 202409264, 202411195, 202504174, 202412175, 202411084, 202509204, 202510114, 202412234, 202409136, 202409134, 202408145, 202409256, 202411085, 202601074, 202501306, 202409024, 202510284, 202406244, 202408015, 202502256, 202506234, 202503074, 202408124, 202502056, 202407024, 202412184, 202410245, 202410255, 202410104, 202409275, 202408144, 202409116. OUS added 06/10/2026 expansion: 202407015, 202506104, 202501024, 202510244, 202511104, 202510274, 202508144, 202510024, 202510104, 202507034, 202507184, 202505054, 202505164, 202506244, 202412064, 202412184, 202408025, 202510254, 202507314, 202507044, 202503244, 202409256, 202509154, 202507315, 202506174, 202510074, 202412175, 202501305, 202504034, 202505154, 202407224, 202407105, 202505014, 202501316, 202502245, 202511065, 202409254, 202411194, 202410254, 202409114, 202511075, 202507214, 202407104, 202601084, 202412054, 202509164, 202504305, 202505294, 202408225, 202407024, 202509084, 202504304, 202502115, 202408054, 202509014, 202410255, 202601094, 202409125, 202408015, 202406245, 202510014, 202410245, 202501315, 202502016, 202410244, 202508284, 202409124, 202503245, 202502134, 202509224, 202502145, 202409136, 202412055, 202411085, 202508014, 202410094, 202507024, 202509194, 202508134, 202507174, 202501154, 202501304, 202501295, 202506114, 202504214, 202506054, 202505176, 202412165, 202409024, 202501025, 202412235, 202408235, 202410165, 202501145, 202406254. Manufactured from 14 June 2024 to 12 January 2026.
• FEI Number: 3001451571
• Recalling Firm/ Manufacturer: ConMed Corporation; 525 French Rd; Utica NY 13502-5945
• Manufacturer Reason for Recall: Potential for overpressure alerts.
• FDA Determined Cause: Process change control
• Action: ConMed notified consignees on about 05/14/2026 via emailed and mailed letter titled URGENT: Medical Device Correction. Consignees were made aware of the issue and risk associated with the issue. They were instructed that a replacement AirSeal disposable should be available prior to procedures in order to minimize potential delays. Before initiating insufflation, the user should ensure the tubing is properly connected between the AirSeal tube set and Airseal Access Ports. If the connection cannot be securely tightened and the overpressure alert cannot be resolved, please replace the affected device. Detailed instructions were provided on how to connect the AirSeal tube set and Airseal Access Ports. Consignees were also instructed to review inventory for affected units, place a copy of the provided Instructions for Use, Part No. AS-DIS-IFU, Rev. B with any inventory in possession with an active expiration date, contact all applicable departments and facilities that may have received affected products for awareness, and complete and return the medical device response form. If further information relevant to this issue becomes necessary CONMED will communicate as such.
• Quantity in Commerce: 29,403 packs (176,418 eaches)
• Distribution: Nationwide distribution
• Total Product Life Cycle: TPLC Device Report

¹ A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
² Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
³ The manufacturer has initiated the recall and not all products have been corrected or removed. This record will be updated as the status changes.

• 510(K) Database: 510(K)s with Product Code = HIF