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 North American subsidiary of Amsterdam-based Royal Philips reached an agreement on a consent decree with the U.S. Department of Justice, representing the Food and Drug Administration, the company ...
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 ...
Health technology company Philips is suspending the manufacture of some defibrillators in the US and will make others under heightened scrutiny following criticisms from US regulators. The Dutch ...
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