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 ...
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 ...
BOTHELL, Washington, Sept. 12, 2012 /PRNewswire/ -- Royal Philips Electronics (NYSE: PHG, AEX: PHI), a pioneer in developing treatments to combat sudden cardiac arrest (SCA), today announced it will ...
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 ...
ANDOVER, Mass., June 3, 2014 /PRNewswire/ -- To mark the 2014 National CPR and AED Awareness Week, Royal Philips is highlighting the importance of access to easy-to-use technology that can help people ...
As we celebrate World Heart Day, Philips celebrates the 20th anniversary of the first automated external defibrillator designed for the layperson with a campaign to raise awareness about sudden ...
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