Lifepak 15 Monitor/defibrillator

Lifepak 15 Monitor/Defibrillator Recall Lifepak 15 Monitor/Defibrillator devices are being recalled in Canada. This is a Class I recall, which is the most serious type. The devices are distributed across Canada and are used in medical settings.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2017-01-25

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/16d14f54-7b4c-4b85-bd33-149cf78d94a0