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 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 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 ...

Certain HeartStart automated external defibrillator (AED) devices made by Philips Medical Systems, a division of Philips Healthcare, may be unable to deliver needed defibrillator shock in a cardiac ...

Philips HeartStart OnSite AEDs help allow anyone with little or no training to treat the most common cause of suspected sudden cardiac arrest (SCA) by delivering a shock quickly and effectively, ...

Royal Philips, a global leader in health technology, announced that the Center for Devices and Radiological Health (CDRH) of the US Food and Drug Administration (FDA) has granted premarket approval ...

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 ...

WAUPACA, Wis. (WBAY) - Gold Cross Ambulance and the “Heartstart Foundation” have installed new life-saving AEDs or “defibrillators” across Waupaca. Ten of the publicly accessible machines are ...

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 ...