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 ...

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 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 ...

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 ...

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 ...

Hundreds of thousands of automated external defibrillators (AEDs) made by Philips Healthcare might not deliver a needed shock to the heart in an emergency, the U.S. Food and Drug Administration said ...

WASHINGTON — Some have called it a jump-starter for the human heart. But the maker of a new automatic external defibrillator wants Americans to think of it as just another safety device for the home - ...

The Philips HeartStart FRx Defibrillator is designed to be easy to set up and use, as well as rugged and reliable for those who get there first. On the scene with law enforcement, on the field with ...

May 2, 2005 — The U.S. Food and Drug Administration (FDA) and Laerdal Medical Corp. have notified healthcare professionals via letter of a recall of all lots of CM 100-Heartstart defibrillator adapter ...