FDAJanuary 13, 2017device

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.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

The firm has received complaints that the LIFEPAK 1000 Defibrillator is unexpectedly powering off during device usage.

What to do

FDA enforcement status: Terminated

Brands named

physio controlphysiophysio control

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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