Physio-Control, Inc. recalls The LIFEPAK 1000 defibrillator is intended for use by person
See all recalls from Physio-Control, Inc. →Recalled Product
The LIFEPAK 1000 defibrillator is intended for use by personnel who are authorized by a physician/medical director and are trained in CPR and the use of the LIFEPAK 1000 defibrillator.
Hazard / Issue
The firm has received complaints that the LIFEPAK 1000 Defibrillator is unexpectedly powering off during device usage.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: Affected Product Part Numbers: 320371500XX. There are 133,330 affected serial numbers.
✅ What Should You Do?
- 1Contact your healthcare provider immediately to discuss this recall.
- 2Stop using the device if it is safe to do so, and contact your provider.
- 3Follow the manufacturer's remedy instructions provided in the recall notice.
- 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.
Looking for a safe alternative?
Search Amazon for The LIFEPAK 1000 defibrillator →If you were harmed by this recalled product, Top Class Actions lists active class action lawsuits and settlements that may apply to you.
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