Philips recently announced that it is voluntarily recalling approximately 5,400 HeartStart FR2+ automated external defibrillators (AEDs). This recall is being conducted due to the possibility of a ...

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 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 ...

October 5, 2009 (Seattle, Washington) — Phillips Medical has issued a recall of about 5400 of its HeartStart FR2+ automated external defibrillators (AEDs), including some models distributed by Laerdal ...

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 ...

AEDs are small, easy-to-use, portable devices that provide treatment for SCA, one of the country's leading medical emergencies and causes of death. Tyson plans to place at least one Philips HeartStart ...

Dubai, UAE, 07 September 2006-Philips Medical Systems is the Platinum Sponsor of The Emergency Congress 2006 scheduled to be held on September 12 -14 2006 at the Bustan Rotana, Dubai. For more than a ...

The Philips HeartStart Fr2+ Defibrillator is engineered to enable anyone to quickly and easily apply life-saving defibrillation therapy to a victim of sudden cardiac arrest. For more than a century ...

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 ...