Z-1232-2025 Class II Ongoing

Recalled by Physio-Control, Inc. — Redmond, WA

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