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Philips Defibrillator Recall

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Phillips is issuing a recall notification due to awareness of isolated failures with one of the device’s electrical components (a resistor). The recall is for the Philips HeartStart FRx, HeartStart OnSite, and HeartStart home defibrillators (AED’s) manufactured between 2002 and 2013. Click here to read the statement put out by the FDA.

 

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