FDA Device recall Z-2470-2026
ConMed AirSeal 5mm Access Port and Low Profile Obturator with Bladeless Optical Tip, 120mm Length
- FDA Device
- Class II
- ongoing
- Published 2026-06-24
On 2026-06-24 the FDA classified a Class II recall of ConMed AirSeal 5mm Access Port and Low Profile Obturator with Bladeless Optical Tip, 120mm Length by Conmed, citing potential for overpressure alerts.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2470-2026 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2026-05-14 |
| Published | 2026-06-24 |
| Last updated | 2026-09-13 11:58 UTC |
| Company | Conmed |
| Distribution | US |
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.
Reason
Potential for overpressure alerts.
Identifiers
| code_info | Catalog Number: iAS5-120LP. UDI-DI: 10845854045657. Lot Numbers: 202504214, 202511075, 202510254, 202510274, 202510244,…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, |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:58 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2470-2026%22
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