Reported Jan 22, 2020 · Terminated
LIFEPAK 15 MONITOR/DEFIBRILLATOR service kits
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 MONITOR/DEFIBRILLATOR service kits
- Lot codes and dates
- Serial numbers
705 of 705 codes
394322833943269439432696394326973943269839432699394327003943270139432702394327193943285439432855394328563943285739432858394328593943286039432862394328633943286439432865394328663943286739432868394328693943287039432871394328723943287339432874394328753943287639432877394328783943287939432881394328823943288339432884394328853943288739432888394328893943289039432893394328963943289739432898394328993943290039432901394353153943658939451160394511613945116439451165394511663945116739451168
- Serial numbers
- Amount recalled
- 705
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Where it was sold
Why it was recalled
Monitor/Defibrillator may not deliver a shock after the "Shock" button on the keypad is pressed as a result of oxidation that has formed over time within the button.
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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