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Physio-Control, Inc. recalls LIFEPAK 15, REF: 99577-001956, Part Number V15-7-000021
Recalled November 22, 2023 · FDA recall Z-0302-2024 · Physio-Control
Hazard
Their is a potential for battery pins to become loose within the defibrillator resulting in power issues. · FDA Class II
Units
1 units
Sold at
US Nationwide distribution in the states of AZ, CA, NC, NJ, NY.
Description
Their is a potential for battery pins to become loose within the defibrillator resulting in power issues.
Product
LIFEPAK 15, REF: 99577-001956, Part Number V15-7-000021
Manufacturer(s)
Physio-Control, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →