Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Heartsine Samaritan PAD: SAM 350P semi-automatic defibrillator Recalled by HeartSine Technologies Ltd Due to Automated external defibrillators were potentially distributed with the...
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 HeartSine Technologies Ltd directly.
Affected Products
Heartsine Samaritan PAD: SAM 350P semi-automatic defibrillator, SAM 360P fully automatic defibrillator, SAM 500P semi-automatic defibrillator with CPR Advisor
Quantity: 13
Why Was This Recalled?
Automated external defibrillators were potentially distributed with the incorrect language configuration, which can lead to a delay in therapy or no therapy.
Where Was This Sold?
This product was distributed to 8 states: AZ, AR, CA, NE, NJ, PA, TX, WI
About HeartSine Technologies Ltd
HeartSine Technologies Ltd has 6 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report