Wednesday, December 4, 2013

FDA warns about faulty Philips HeartStart defibrillators

The Food and Drug Administration (FDA) is warning consumers that some models of HeartStart automated external defibrillators (AED) may not work during a cardiac emergency. The devices, which are made by Philips Medical Systems, a division of Philips Healthcare, had previously been recalled, but…

Source:FDA warns about faulty Philips HeartStart defibrillators



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