FDA-Device2013-04-17Class II
The LIFEPAK CR Plus and LIFEPAK EXPRESS defibrillators. Product part's numbers: 3200731-xxx, 3202177-xxx, U3200731-xxx, and U3202177-006. Automated external defibrillators.
Physio Control, Inc.
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.
Sold states
Worldwide Distribution.
Affected count
54,197 units in US and 78,627 units internationally (total 132, 824 units)
Manufactured in
11811 Willows Rd Ne, Redmond, WA, United States
Products
The LIFEPAK CR Plus and LIFEPAK EXPRESS defibrillators. Product part's numbers: 3200731-xxx, 3202177-xxx, U3200731-xxx, and U3202177-006. Automated external defibrillators.
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1082-2013Don't want to check this manually?
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