Lifepak 35 Monitor/defibrillator

LIFEPAK 35 Monitor/Defibrillator Recall The LIFEPAK 35 Monitor/Defibrillator is being recalled in Canada due to a performance issue with the device. This Class I recall affects units distributed across Canada. The device is used to monitor heart activity and deliver electrical therapy to restore normal heart rhythm.

Product

LIFEPAK 35 Monitor/Defibrillator

Reason

Performance

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2025-08-27

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/0b364a71-6c95-4a3d-a04d-9ebb58502111