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 ...

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 ...

The US Food and Drug Administration (FDA) is classifying a recent safety notice covering certain models of the HeartStart MRx Monitor/Defibrillator due to electrical and battery connection issues as a ...

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 ...

A recent study has shown that one-year mortality rates for acute myocardial infarction (AMI, i.e. a heart attack) increase when treatment by a primary angioplasty is delayed. As soon as a heart attack ...

MedStar EMS, the 911 provider of Fort Worth, and 14 surrounding cities, has outfitted its fleet of emergency vehicles with Philips HeartStart MRx Monitor/Defibrillators with Q-CPR technology, to ...

Royal Philips Electronics (NYSE:PHG, AEX:PHI) today announced that several leading-edge U.S. emergency medical service (EMS) organizations have chosen the Philips HeartStart MRx – an advanced, ...

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 ...

Add articles to your saved list and come back to them any time. St John Ambulance WA is suing an Australian medical supplier over claims it was sold nearly $5 million worth of defibrillators not ...

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 ...