Reported Jun 4, 2014 · Terminated
LIFEPAK 1000 defibrillator. Affected Part Numbers: 320371500XXX The LP1000 (in AED mode) is indicated for use on…
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 1000 defibrillator
- Affected Part Numbers320371500XXX The LP1000 (in AED mode) is indicated for use on patients in cardiac arrest
- Lot codes and dates
- Affected Part Numbers320371500XXX *****SERIAL NUMBERS FOR US DEPARMENT OF DEFENSE***********SERIAL NUMBERS FOR VETERANS HOSPITALS****************
2,243 of 2,243 codes
348760343487603834876056348760643487606534877573348775743487757534877576348775783487758234988650349886513512213935147830352151233521512435908182359081833597262135972622359726233597262435972625360596543606589136065892360658933606589436065895360658963606589736065898360662913606629236066322360663233606632636066330360663313606633236066530360665693606657136066575360666763608512536089293360892943608929536089297361032343610323536103236361032373610323836103239361032403610324136103242
*******SERIAL NUMBERS FOR US CONSIGNEES***********************889 of 889 codes
349930503499305134993052349930533499305434993055349930563499305734993058349930593499306034993061349930623499306336269635362700283627002936461588364615893646159036567832365678393656784036567841365678503656785936567937365691143670525036705251367052523670525336705254367052553671483136714832367148333671483436967242369750363697503736975038369750393697504036975041369750423697504336975044369750453697504636975047369763383700417937004180370643993706440037067412370674133707707037077727
106 of 106 codes
12972323289415732895126328951303289513632895306328953173289543733468929345879023458790334587904345879053458790634587908345879093458791034587911345879123458791334587914345879153458791634587917345879183458791934588709345887103458871134588712345887133458871434588716345887183458871934588731345893523458935334684302346843033468430434684305346843253468487934686190346862343468623534686236346862373468623834686239346862403468624134686242346862433468624434686245346862463468624734686248
- Affected Part Numbers320371500XXX *****SERIAL NUMBERS FOR US DEPARMENT OF DEFENSE******
- Amount recalled
- 96,611 units total (40,974 in the US and 55,637 outside the US)
Where it was sold
- Nationwide
- GA
Why it was recalled
Physio-Control has become aware of incidents where customers have attempted to use their LIFEPAK 1000 defibrillator and the device has shut down unexpectedly due to a very low battery. A defibrillator in this scenario has the potential to fail to deliver a shock, with the potential result that therapy is not delivered and a patient is not resuscitated. A software malfunction in the LIFEPAK 100
This product could cause temporary or reversible health problems — stop using it.
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