Class III — Low Risk

Low risk — use of or exposure to this product is not likely to cause adverse health consequences.

HeartSine Samaritan PAD Recalled by Physio-Control, Inc. Due to Semi-automatic defibrillators shipped out by Stryker without battery...

Date: January 13, 2022
Company: Physio-Control, Inc.
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Physio-Control, Inc. directly.

Affected Products

HeartSine Samaritan PAD, SAM 350P Semi-Automatic Defibrillator, used with Pad-Pak

Quantity: 1

Why Was This Recalled?

Semi-automatic defibrillators shipped out by Stryker without battery and electrode packs.

Where Was This Sold?

This product was distributed to 1 state: AK

Affected (1 state)Not affected

About Physio-Control, Inc.

Physio-Control, Inc. has 38 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report