Reported Apr 17, 2013 · Terminated
The LIFEPAK CR Plus and LIFEPAK EXPRESS defibrillators. Product part's numbers: 3200731-xxx, 3202177-xxx, U3200731-xxx,…
Physio Control, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Physio Control, Inc. · 11811 Willows Rd Ne · Redmond, WA · 98052-2003
Is this the product you have?
- The LIFEPAK CR Plus and LIFEPAK EXPRESS defibrillators
- Product part's numbers3200731-xxx, 3202177-xxx, U3200731-xxx, and U3202177-006. Automated external defibrillators
- Lot codes and dates
- Serial numbers
- of devices distributed in the US
3,255 of 3,255 codes
332192513322031033220344332203673322036933220376332204023322045033220461332204643322046633220470332212003322139433231481332314863323148833231492332315113323151233231521332315233323152433231527332315323323153533231536332315393323154533231546332315543323161133231614332316183323162333231625332316283323163533231636332316393323164133231685332317123323172833231733332317373323174133231745332317553323175833232813332328143323281633237363332388093323910433239111332391183323912533239127
- Amount recalled
- 54,197 units in US and 78,627 units internationally (total 132, 824 units)
Why it was recalled
LIFEPAK CR Plus or LIFEPAK Express Automated External Defibrillators (AEDs) are recalled due to the potential to experience an early internal battery depletion issue.
This product could cause temporary or reversible health problems — stop using it.
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