Airlife Adult Manual Resuscitator

Airlife Adult Manual Resuscitator Recall Airlife Adult Manual Resuscitator devices are being recalled in Canada due to performance issues. This device is used to manually deliver breaths to patients who are not breathing adequately. The recall affects units distributed across Canada.

Product

Airlife Adult Manual Resuscitator

Reason

Performance

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2024-04-05

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/1d679690-eb6c-45a1-a69b-3ac5d0bed207