FDA-Device2025-03-05Class II
LIFEPAK 20e REF 99507-000001 The AED mode is to be used only on patients in cardiopulmonary arrest.
Physio-Control, Inc.
Hazard
Incorrect keypad was incorrectly installed onto a defibrillator/monitor.
Sold states
U.S.: WV O.U.S.: N/A
Affected count
1
Manufactured in
11811 Willows Rd Ne, N/A, Redmond, WA, United States
Products
LIFEPAK 20e REF 99507-000001 The AED mode is to be used only on patients in cardiopulmonary arrest.
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1232-2025Don't want to check this manually?
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