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
    • CR2-2-001281
    • CR2-2-001279
    • CR2-2-001285
    • CR2-2-001278
    • CR2-2-001283
    • CR2-2-001280
    • CR2-2-001451
    • CR2-2-001452
    • CR2-2-000396
    • CR2-2-001457
  • Device Serial Numbers

    3,235 of 3,235 codes

    • 48603094
    • 48784877
    • 49025132
    • 49091799
    • 48741587
    • 49077058
    • 48764540
    • 48764590
    • 48601446
    • 48603907
    • 48609453
    • 48652129
    • 48652251
    • 48858056
    • 48981644
    • 48722045
    • 48726027
    • 48726129
    • 48726140
    • 48726150
    • 48693695
    • 48694311
    • 48698571
    • 48698584
    • 48952116
    • 48953086
    • 48554965
    • 48817780
    • 48825290
    • 48849399
    • 48899908
    • 48899994
    • 48900065
    • 48900096
    • 48901342
    • 48901357
    • 48901414
    • 48901451
    • 48902351
    • 48977818
    • 48978218
    • 48981319
    • 48981675
    • 48981678
    • 48981736
    • 48981742
    • 48981757
    • 48981799
    • 48982659
    • 48982689
    • 48982706
    • 48982732
    • 48982753
    • 48982964
    • 48983131
    • 48983138
    • 48986526
    • 48999915
    • 49001794
    • 48677566
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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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 6:59 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.