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 ...
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 ...
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 ...
[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 ...
SEATTLESEATTLE — Philips Healthcare said Saturday 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 ...
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