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 ...

Please provide your email address to receive an email when new articles are posted on . The FDA has issued a safety communication indicating that certain HeartStart automated external defibrillators ...

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 ...

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 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 ...

PUNTA GORDA, FL / ACCESSWIRE / January 11, 2017 / The founders of ACC Medlink, a leader in medical transportation, are pleased to announce that their nationwide medical transport vehicles are now ...

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 ...

Gaithersburg, MD - The push for over-the-counter defibrillators is gathering momentum. A US Food and Drug Association panel heard arguments yesterday for removing the prescription requirement for the ...