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/MONITOR
    • 3201273
  • 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

    • 45039371
    • 45041785
    • 45044636
    • 45057093
    • 45067882
    • 45073270
    • 45450645
    • 45491315
    • 45491441
    • 45491644
    • 45808476
    • 45813092
    • 45598878
    • 45599806
    • 45073745
    • 45435012
    • 45439562
    • 45278002
    • 45307727
    • 45307732
    • 45307742
    • 45308078
    • 45309308
    • 45309310
    • 45309317
    • 45309923
    • 45310487
    • 45310523
    • 45489720
    • 45321756
    • 45605113
    • 45167375
    • 45160349
    • 45540221
    • 45066559
    • 45551722
    • 45253909
    • 45635361
    • 45313588
    • 45314492
    • 45321757
    • 45173154
    • 45807047
    • 45694119
    • 45041460
    • 45041335
    • 45041572
    • 45486374
    • 45439205
    • 45451242
    • 45468563
    • 45860139
    • 45321722
    • 45399194
    • 45040553
    • 45937962
    • 45860005
    • 45889371
    • 45890053
    • 45890181
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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Where this came from

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

Read the FDA (openFDA device enforcement) notice

Notice updated Apr 1, 2024 · Data as of Sep 19, 6:06 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.