Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Pad-Pak and Pedi-Pak accessories for the HeartSine Samaritan PAD 300P Recalled by Heartsine Technologies, Limited Due to A small number of sealed foil pouches containing...
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, Limited directly.
Affected Products
Pad-Pak and Pedi-Pak accessories for the HeartSine Samaritan PAD 300P and 350P device (SAM 300P and 350P). Automated External Defibrillator electrode supplies. The Pedi-Pak is specifically designed for use with the HeartSine Samaritan PAD 300P and 350P device. It contains defibrillator electrodes in a sealed foil pouch and a battery pack in a sealed plastic housing.
Quantity: 3245
Why Was This Recalled?
A small number of sealed foil pouches containing the electrodes were found to be difficult to open, resulting in potential delay in therapy.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Heartsine Technologies, Limited
Heartsine Technologies, Limited has 2 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report