Lifepak 15 Monitor/defibrillator

Lifepak 15 Monitor/Defibrillator Recall Lifepak 15 Monitor/Defibrillator devices are being recalled across Canada. This is a Class I recall, which is the most serious type. The devices are used in medical settings to monitor heart rhythm and deliver electrical shocks when needed.

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/27fcd313-2acb-4ac7-b1a3-fb4b21205514