SEATTLESEATTLE — Philips said Monday it is recalling about 5,400 HeartStart FR2 automated external defibrillators due to a possible memory chip failure that could make the device unable to work ...

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 ...

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 therapy delivered by the HeartStart FR2+ is the most proven in the industry. More than 40 studies confirm its effectiveness. Philips’ high-current/low energy therapy ensures a potent ...

Since officers are often first to arrive at the scene of a cardiac emergency, it is crucial to have immediate access to an AED in the event the victim is experiencing SCA. Defibrillation is recognized ...

Philips recalled its HeartStart MRx Defibrillator due to an equipment defect, according to a Feb. 9 safety notice from the FDA. Here are three things to know. 1. Philips initiated the recall in June ...

The Philips HeartStart OnSite Defibrillator is designed to be the easiest-to-use, and most reliable defibrillator available. Available without a prescription from ActiveForever.com, the Philips ...

27 October 2007 Dubai- UAE - Philips and ARASCA Medical Equipments Trading LLC donated 2 HeartStart FRx Defibrillators unites to the rescue team of the UAE Desert Challenge.The UAE Desert Challenge ...

Amsterdam, the Netherlands –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 Food and Drug ...

ANDOVER, Mass., June 23 /PRNewswire/ -- Royal Philips Electronics (NYSE: PHG, AEX: PHI) announced today that six U.S. law enforcement agencies have acquired its HeartStart FRx Automated External ...