Recall Z-0567-2024— Physio-Control, Inc.

Name: FDA recall Z-0567-2024
Creator: U.S. Food and Drug Administration
Published: 2023-11-06

Class II · Ongoing

Class II FDA medical device recall by Physio-Control, Inc., initiated 2023-11-06. FDA's recall record names no specific 510(k) clearance for this event. Product: AC Power Adapter for use with the LIFEPAK 15 Monitor/Defibrillator, REF: 11140-000098. Reason: AC Power Adapter (ACPA) may not charge the monitor/defibrillator batteries and may not allow the monitor/defibrillator to power on while plugged into the ACPA..

Recalling firm: Physio-Control, Inc.
Classification: Class II
Status: Ongoing
Initiated: 2023-11-06
Firm location: Redmond, WA, United States

Product description

AC Power Adapter for use with the LIFEPAK 15 Monitor/Defibrillator, REF: 11140-000098

Reason for recall

AC Power Adapter (ACPA) may not charge the monitor/defibrillator batteries and may not allow the monitor/defibrillator to power on while plugged into the ACPA.

Data sourced from openFDA. This site is unofficial and independent of the FDA.