The U.S. Food and Drug Administration has issued a safety communication saying certain HeartStart automated external defibrillator devices made by Philips Medical Systems, a division of Philips ...
According to a press release from the FDA, certain HeartStart automated external defibrillators (AEDs) may not be able to deliver the necessary shock in a cardiac emergency. The FDA released this ...
Federal health regulators in the U.S. are warning the public that certain cardiac defibrillators recalled by Philips Healthcare may fail to deliver a needed shock in an emergency. Defibrillators are ...
The U.S. Food and Drug Administration has flagged three of Philips' medical device facilities after inspections found they ...
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