Heartsine® Samaritan® Pad Sam 350p/sam 360p/sam 500p - Membrane Tail

Recall Summary HeartSine Samaritan PAD defibrillator models SAM 350P, SAM 360P, and SAM 500P are being recalled in Canada due to a device performance issue with the membrane tail component. The recall affects units distributed across Canada. This is classified as a Class II recall, indicating a device malfunction that could result in serious injury but is not immediately life-threatening.

Product

HeartSine® Samaritan® PAD SAM 350P/SAM 360P/SAM 500P Defibrillator - Membrane Tail

Reason

Device performance issue

Classification

Class II

Category

medical device recall

Country

Canada

Agency

HC-DEVICES

Recall date

2026-07-23

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/1b8d6f12-62c7-4dba-832c-63a44d3bbfa2