Reported Jan 22, 2020 · Terminated
LIFEPAK 15 MONITOR/DEFIBRILLATOR that was either manufactured with or received an upgrade kit that contained an…
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 that was either manufactured with or received an upgrade kit that contained an affected keypad.
- Lot codes and dates
- Serial numbers
3,259 of 3,259 codes
379646133796461737964621379646283796463037968424379684293796459637964601379646073796461037968715379687163796871737968718379687213796872237968724380465403804654938046552380465653804657138046572380465733805194938051951380519543805195538051958380519633805196938051972380519733805197438051980380532163805321838053220380532213805322538053231380532333805323638053239380595683805957038059574380595913812076938120772381207753812078038120781381207833812078438120787381207883812079038124016
- Serial numbers
- Amount recalled
- 29952
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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