Reported Mar 17, 2021 · Ongoing
PHYSIO CONTROL LIFEPAK CR2 Defibrillator 3321605-xxx The LIFEPAK CR2 defibrillator is designed for indoor and outdoor…
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?
- PHYSIO CONTROL LIFEPAK CR2 Defibrillator 3321605-xxx The LIFEPAK CR2 defibrillator is designed for indoor and outdoor use in a stationary environment. After the electrode pads are applied, the fully automatic model evaluates the heart rhythm and, if a shockable rhythm is detected, delivers a shock without any responder assistance. The LIFEPAK CR2 defibrillator is indicated for use on patients 1 year of age or older in cardiopulmonary arrest.
- Lot codes and dates
- Model Number 3321605-xxx, U.S. Device
- Part Numbers with Conforming Lids
CR2-2-001281CR2-2-001279CR2-2-001285CR2-2-001278CR2-2-001283CR2-2-001280CR2-2-001451CR2-2-001452CR2-2-000396CR2-2-001457
- Device Serial Numbers
3,235 of 3,235 codes
486030944878487749025132490917994874158749077058487645404876459048601446486039074860945348652129486522514885805648981644487220454872602748726129487261404872615048693695486943114869857148698584489521164895308648554965488177804882529048849399488999084889999448900065489000964890134248901357489014144890145148902351489778184897821848981319489816754898167848981736489817424898175748981799489826594898268948982706489827324898275348982964489831314898313848986526489999154900179448677566
- Amount recalled
- 89,763 units
Where it was sold
Why it was recalled
Due to complaints received regarding missing lid magnets which may result in premature battery depletion.
This product could cause temporary or reversible health problems — stop using it.
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