FDASeptember 29, 2023device

LIFEPAK 15, REF: 99577-000061, Part Number V15-2-000067

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

The hazard

Their is a potential for battery pins to become loose within the defibrillator resulting in power issues.

What to do

FDA enforcement status: Ongoing

Brands named

physio controlphysiophysio control

UPCs

0088387397935899577000061

Recall history

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

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LIFEPAK 15, REF: 99577-000061, Part Number V15-2-000067 — Recall Details · AllClear