Irlife Infant Manual Resuscitator

Airlife Infant Manual Resuscitator Recall Summary Airlife Infant Manual Resuscitators are being recalled across Canada because they may not deliver the correct oxygen concentration or tidal volume when used, which could affect their ability to properly assist with patient breathing. This recall affects medical devices that were distributed throughout Canada. The issue applies to Airlife Infant Manual Resuscitators used in healthcare settings.

Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2017-06-21
Status
Closed
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/75f06f04-c266-45c0-8b90-9af9bd6852c1