The U.S. Food and Drug Administration has issued a safety communication saying certain HeartStart automated external defibrillator devices made by Philips Medical Systems, a division of Philips ...
Washington DC - The FDA has granted marketing clearance to an automatic external defibrillator (AED) intended specifically for home use. Philips Electronics calls its HeartStart Home Defibrillator the ...
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, ...
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 ...
HealthDay News — The FDA is advising owners of Philips HeartStart automated external defibrillator (AED) devices to contact the company to ascertain whether their device is among those that might be ...
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 ...
It is an advanced defibrillator equipped with groundbreaking Real CPR Help technology. This innovative device guides rescuers in administering high-quality CPR and stands ready to deliver a ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results