Airseal Access Port With Blunt Obturator And Airseal Access Port With Optical Obturator

Recall Summary AirSeal Access Ports with both blunt and optical obturators are being recalled across Canada due to a device performance issue. These are medical devices used during surgical procedures. The recall is classified as Class II, indicating a potential health risk that could result in temporary or reversible effects.

Product

AirSeal Access Port With Blunt Obturator and AirSeal Access Port With Optical Obturator

Reason

Device performance issue

Classification

Class II

Category

medical device recall

Country

Canada

Agency

HC-DEVICES

Recall date

2026-07-02

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/30554a66-c49a-45ed-8c4a-66007d4192a7