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 ...

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 ...

Amsterdam, the Netherlands and Cambridge, MA – Royal Philips (NYSE: PHG, AEX: PHIA), a global leader in health technology, today announced that the Center for Devices and Radiological Health (CDRH) of ...

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 ...

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 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 ...

Certain HeartStart automated external defibrillator devices made by Philips Medical Systems might be unable to deliver needed defibrillator shocks in a cardiac emergency, the Food and Drug ...

Clever design, close attention to human safety issues, and a top man-machine interface make the Philips HeartStart portable home defibrillator one of the hottest medical electronics devices on the ...

SILVER SPRING, Md. — The Food and Drug Administration on Tuesday issued a safety communication on HeartStart automated external defibrillators from Philips Healthcare, noting that certain HeartStart ...