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 ...
WASHINGTON – Federal health regulators are warning the public that certain cardiac defibrillators recalled by Philips Healthcare may fail to deliver a needed shock in an emergency. Defibrillators are ...
Amsterdam, the Netherlands – Royal Philips (NYSE: PHG, AEX: PHIA), a global leader in health technology, announced today that its Emergency Care and Resuscitation (ECR) business is resuming ...
In case your fibrillator need defibrillating, Philips is poised to bring this automatic defibrillator to market once the FDA approves direct-to-consumer sales of the devices. You've seen these on ER ...
Philips Healthcare said today it is recalling about 5,400 automated external defibrillators after receiving reports of a memory chip failure in a small number of some models that could make them ...
[THE HAGUE] Dutch electronics giant Philips announced Wednesday it is temporarily suspending production of defibrillators for the US market to allow closer inspections in a deal reached with the ...
AMSTERDAM (MarketWatch) -- Royal Philips Electronics NV PHG recalled 2,000 of its defibrillators in the second half of 2006 after the U.S. Food and Drug Administration (FDA) found technical failures ...
We know what you're thinking: not another talking defibrillator, but the Q-CPR add-on to Philips' HeartStart MRx monitor/defibrillator actually happens to be the first of its kind, and was recently ...
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