Lifepak 15 Monitor/defibrillator

LIFEPAK 15 Monitor/Defibrillator Recall Summary Philips is recalling LIFEPAK 15 monitor/defibrillator devices in Canada because the device may not deliver therapy or may delay therapy delivery during a cardiac emergency. This recall affects medical facilities and emergency responders across Canada that use this equipment.

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2016-09-09

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/cba61cbd-e19a-4c54-b858-7a65cba7152f