SEATTLESEATTLE — Philips said Monday it is recalling about 5,400 HeartStart FR2 automated external defibrillators due to a possible memory chip failure that could make the device unable to work ...
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 ...
Certain HeartStart automated external defibrillator devices made by Philips Medical Systems might be unable to deliver needed defibrillator shocks in a cardiac emergency, the Food and Drug ...
Gaithersburg, MD - The push for over-the-counter defibrillators is gathering momentum. A US Food and Drug Association panel heard arguments yesterday for removing the prescription requirement for the ...
11 June 2006 Dsseldorf, Germany - As part of its sponsorship of the 2006 FIFA World Cup, Royal Philips Electronics (NYSE: PHG, AEX: PHI) is providing all 32 qualified teams as well as the 2006 World ...
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