Lifepak 1000 Defibrillator Field Action [US]

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US/Silver Spring: Lifepak 1000 Defibrillator Field Action [US]Physio-Control issues a Voluntary Field Action for all current Lifepak 1000 Defibrillators due to suspected operational failure, unexpectedly shut-down during patient treatment and possible death, a serious health hazard. FDA:

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Additional information:
The US Food and Drug Administration (“FDA”) reports the following Medical Devices are subject to this Field Action:

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