FDAFebruary 3, 2025device

LIFEPAK 20e REF 99507-000001 The AED mode is to be used only on patients in cardiopulmonary arrest.

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

The hazard

Incorrect keypad was incorrectly installed onto a defibrillator/monitor.

What to do

FDA enforcement status: Ongoing

Brands named

physio controlphysiophysio control

UPCs

9950700000100883873813751

Recall history

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

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