FDA Device recall Z-2465-2026
ConMed AirSeal 12 mm Access Port and Obturator with Blunt 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 12 mm Access Port and Obturator with Blunt Tip, 120mm Length by Conmed, citing potential for overpressure alerts.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2465-2026 |
| 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 12 mm Access Port and Obturator with Blunt Tip, 120mm Length. Catalog Number: iASB12-120. 6 units per pack. Disposable Endoscopic Trocar and Cannula; Carbon Dioxide Insufflator for Laparoscopy.
Reason
Potential for overpressure alerts.
Identifiers
| code_info | Catalog Number: iASB12-120. UDI-DI: 10845854045725. Lot Numbers: 202507314, 202506194, 202510024, 202501165, 202504034,…Catalog Number: iASB12-120. UDI-DI: 10845854045725. Lot Numbers: 202507314, 202506194, 202510024, 202501165, 202504034, 202408225, 202411264. *OUS added 06/10/2026 expansion: 202510024, 202507314, 202504034, 202501165, 202411264, 202408225, 202506194. Manufactured from 14 June 2024 to 12 January 2026. |
|---|
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-2465-2026%22
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