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FDAFebruary 1, 2023device

Heartsine Samaritan PAD: SAM 350P semi-automatic defibrillator, SAM 360P fully automatic defibrillator, SAM 500P semi-automatic defibrillator with CPR Advisor

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Automated external defibrillators were potentially distributed with the incorrect language configuration, which can lead to a delay in therapy or no therapy.

What to do

FDA enforcement status: Ongoing

Brands named

heartsine technologiesheartsine

UPCs

050601671206715060167127120506016712802850601671265055060167125843

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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