FDA Enforcement Class II Ongoing

LIFEPAK 1000 Part / Catalog Numbers / UDI-DI code: 320371500023 / 99425-000025 / 885074698953 320371500229 / 99425-000025 / 885074698953 331706400001 / 99425-000025 / 885074698953 LIFEPAK 1000: The defibrillator is to be used in AED mode only on patients who are in cardiopulmonary arrest. The patient must be unresponsive, not breathing normally, and showing no signs of circulation. ECG monitoring is for use on conscious and unconscious patients of all ages for the purpose of ECG rhythm recognition and heart rate monitoring.

Recall: Z-2498-2025 · Reported September 10, 2025

Enforcement

Recall Number
Z-2498-2025
Event ID
96949
Classification
Class II
Status
Ongoing
Product Type
Devices
Firm
Physio-Control, Inc.
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
N/A
Report Date
September 10, 2025
Initiation Date
July 22, 2025
Classification Date
September 2, 2025
Address
11811 Willows Rd Ne, N/A, Redmond, WA, 98052-2003, United States

Description

LIFEPAK 1000 Part / Catalog Numbers / UDI-DI code: 320371500023 / 99425-000025 / 885074698953 320371500229 / 99425-000025 / 885074698953 331706400001 / 99425-000025 / 885074698953 LIFEPAK 1000: The defibrillator is to be used in AED mode only on patients who are in cardiopulmonary arrest. The patient must be unresponsive, not breathing normally, and showing no signs of circulation. ECG monitoring is for use on conscious and unconscious patients of all ages for the purpose of ECG rhythm recognition and heart rate monitoring.

Reason

Due to required inspections not being performed on products/units that have gone through servicing.

Code Info

Part / Catalog Numbers / UDI-DI code / Serial Number: 320371500023 / 99425-000025 / 885074698953 / 35942190 320371500229 / 99425-000025 / 885074698953 / 41012118 331706400001 / 99425-000025 / 885074698953 / 48988273

Distribution

U.S. Nationwide distribution in the states of CO and MT.

Quantity

3 units