Reported Nov 22, 2023 · Ongoing
LIFEPAK 15, REF: 99577-000055, Part Number V15-2-000061
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?
- LIFEPAK 15
- REF
99577-000055Part Number V15-2-000061
- Lot codes and dates
- UDI00883873979426/
- Serial number
3829054038291328383153113831531438324196383241993833234538898631
- Amount recalled
- 8 yrs.
This recall covers 10 products
The agency filed one notice per product. You are reading one of them; the other 9 are below.
Where it was sold
Why it was recalled
Their is a potential for battery pins to become loose within the defibrillator resulting in power issues.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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