Class II
Medical Device Recall: LIFEPAK 20e REF 99507-000001 The AED mode is to be used only on patients in cardiopulmonary arrest.
Physio-Control, Inc. · February 3, 2025
Reason for Recall
Incorrect keypad was incorrectly installed onto a defibrillator/monitor.
Distribution
U.S.: WV O.U.S.: N/A
States Affected
WV
Quantity Affected
1
Source: FDA (openFDA Device Enforcement)
Recall number: Z-1232-2025
Status: ongoing
SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.