FDAApril 13, 2026device

LIFEPAK 15, REF: 99577-000025, 99577-000047, 99577-001256, 99577-001217, 99577-001241, 99577-001255, 99577-001219, 99577-001957, 99577-001935, 99577-001964, 99577-001955, 99577-001956, 99577-001588, 99577-001958, 99577-001950, 99577-001962, 99577-002178, 99577-001372, 99577-001938, 99577-000045; ...

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

The hazard

Some defibrillators serviced between July 2023 through November 2025 were serviced without objective evidence that a Performance Inspection Procedure (PIP) was conducted, and the inability to perform the device's intended use may result in potential harms such as delays or inability to provide therapy.

What to do

FDA enforcement status: Ongoing

Brands named

physio controlphysiophysio control

UPCs

995770000259957700004799577001256995770012179957700124199577001255995770012199957700195799577001935995770019649957700195599577001956

Recall history

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

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