A faulty electronic component in some Philips HeartStart automated external defibrillators may prevent the device from delivering a needed shock to a person suffering a cardiac emergency, the FDA ...

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 ...

LONDON — Koninklijke Philips Electronics NV (Amsterdam, The Netherlands), a leading vendor of consumer and medical products, has announced that it is recalling approximately 5,400 HeartStart FR2+ ...

AMSTERDAM (Reuters) - Health technology company Philips is suspending the manufacture of some defibrillators in the United States and will make others under heightened scrutiny following criticisms ...

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 ...

OpenMarkets, a collaborative marketplace for capital medical equipment, has announced multiple providers have already taken advantage of its recently launched OpenMarkets MarketBuy for Philips ...

ANDOVER — A federal court ordered Philips North America, headquartered in Andover, to cease distributing certain models of its automated external defibrillators until the company complies with federal ...

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 could make them ...

On August 3, 2017, a Boston jury awarded Philips $10.4 million in damages for ZOLL’s infringement of three patents relating to automated external defibrillators. This represents only a fraction of the ...

Philips Healthcare, which is headquartered in Andover, is voluntarily recalling approximately 5,400 automated external defibrillators because of a faulty memory chip. Four models of the so-called ...