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 ...

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 ...

Laerdal Medical Corp. is recalling more than 3,000 defibrillator adapter cables, sold nationwide since 1996, after receiving reports that broken wires in the cables prevented delivery of shocks to ...

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 ...

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 ...

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 ...

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 ...

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 ...

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 ...