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 ...
SILVER SPRING, Md. — The Food and Drug Administration on Tuesday issued a safety communication on HeartStart automated external defibrillators from Philips Healthcare, noting that certain HeartStart ...
Philips recently announced that it is voluntarily recalling approximately 5,400 HeartStart FR2+ automated external defibrillators (AEDs). This recall is being conducted due to the possibility of a ...
The US Food and Drug Administration (FDA) is classifying a recent safety notice covering certain models of the HeartStart MRx Monitor/Defibrillator due to electrical and battery connection issues as a ...
Amsterdam, the Netherlands and Cambridge, MA – Royal Philips (NYSE: PHG, AEX: PHIA), a global leader in health technology, today announced that the Center for Devices and Radiological Health (CDRH) of ...
The Philips HeartStart FRx Defibrillator is designed to be easy to set up and use, as well as rugged and reliable for those who get there first. On the scene with law enforcement, on the field with ...
Clever design, close attention to human safety issues, and a top man-machine interface make the Philips HeartStart portable home defibrillator one of the hottest medical electronics devices on the ...
Please provide your email address to receive an email when new articles are posted on . The FDA has issued a safety communication indicating that certain HeartStart automated external defibrillators ...
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