Z-1232-2025 Class II Ongoing
Recall Details
- Product Type
- Devices
- Report Date
- March 5, 2025
- Initiation Date
- February 3, 2025
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 1
Product Description
LIFEPAK 20e REF 99507-000001 The AED mode is to be used only on patients in cardiopulmonary arrest.
Reason for Recall
Incorrect keypad was incorrectly installed onto a defibrillator/monitor.
Distribution Pattern
U.S.: WV O.U.S.: N/A
Code Information
Model/Catalog Number: 99507-000001 UDI-DI code: 00883873813751 Serial Number: 38289467