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Physio Control, Inc. recalls The LIFEPAK CR Plus and LIFEPAK EXPRESS defibrillators. Product part's numbers: 3200731-xxx, 3202177-xxx, U3200731-xxx,
Recalled April 17, 2013 · FDA recall Z-1082-2013 · Physio Control
Hazard
LIFEPAK CR Plus or LIFEPAK Express Automated External Defibrillators (AEDs) are recalled due to the potential to experience an early internal battery depletion issue. · FDA Class II
Units
54,197 units in US and 78,627 units internationally (total 132, 824 units)
Sold at
Worldwide Distribution.
Description
LIFEPAK CR Plus or LIFEPAK Express Automated External Defibrillators (AEDs) are recalled due to the potential to experience an early internal battery depletion issue.
Product
The LIFEPAK CR Plus and LIFEPAK EXPRESS defibrillators. Product part's numbers: 3200731-xxx, 3202177-xxx, U3200731-xxx, and U3202177-006. Automated external defibrillators.
Manufacturer(s)
Physio Control, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →