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Physio-Control, Inc. recalls LIFEPAK 20e REF 99507-000001 The AED mode is to be used only on patients in cardiopulmonary arrest.
Recalled March 5, 2025 · FDA recall Z-1232-2025 · Physio-Control
Hazard
Incorrect keypad was incorrectly installed onto a defibrillator/monitor. · FDA Class II
Units
1
Sold at
U.S.: WV O.U.S.: N/A
Description
Incorrect keypad was incorrectly installed onto a defibrillator/monitor.
Product
LIFEPAK 20e REF 99507-000001 The AED mode is to be used only on patients in cardiopulmonary arrest.
Manufacturer(s)
Physio-Control, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →