Reported Jan 17, 2018 · Terminated
LIFEPAK 20e DEFIBRILLATOR/MONITOR, 3201273 Product Usage: The LIFEPAK 20e defibrillator/monitor is intended for use in…
Physio-Control, Inc.
High riskUsing this product could cause serious injury, illness or death — stop using it now.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 20e DEFIBRILLATOR/MONITOR3201273
- Product UsageThe LIFEPAK 20e defibrillator/monitor is intended for use in the hospital, physician s office, and clinic setting by personnel who are authorized by a physician/medical director. It is intended for use on a crash cart as well as for portable emergency response throughout a hospital
- Lot codes and dates
3,260 of 3,260 codes
450393714504178545044636450570934506788245073270454506454549131545491441454916444580847645813092455988784559980645073745454350124543956245278002453077274530773245307742453080784530930845309310453093174530992345310487453105234548972045321756456051134516737545160349455402214506655945551722452539094563536145313588453144924532175745173154458070474569411945041460450413354504157245486374454392054545124245468563458601394532172245399194450405534593796245860005458893714589005345890181
- Amount recalled
- 3831 units
Why it was recalled
Stop using this product now
Physio-Control is aware that some devices have had power-related failures as customers prepared their device for initial deployment or during use within the first year of distribution. The symptoms of these failures may include unexpected power on and power off, device lock-up, or a failure to power on or off, any of which has the potential to result in a failure to deliver therapy to the patient and serious injury or death.
Using this product could cause serious injury, illness or death — stop using it now.
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