The FDA first approved home models of Philips AED devices in 2004. The defibrillators under question were manufactured and distributed between 2005 and 2012 under the names HeartStart FRx ...

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 ...

Philips recalled its HeartStart MRx Defibrillator due to an equipment defect, according to a Feb. 9 safety notice from the FDA. Here are three things to know. 1. Philips initiated the recall in ...

June 23, 2020Amsterdam, the Netherlands and Cambridge, MA – Royal Philips (NYSE: PHG, AEX: PHIA), a global leader in health technology, today anno ...

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 ...

Hodge explains how the Philips HeartStart model, the current model provided in Huntsville Center facilities, gives verbal and written instructions for a step-by-step approach to handling emergencies.

ASHI certified training center and AED program oversight for the university. W&M menu. Close menu. Search. Submit Search. Hit enter to search all of wm.edu. ... This short video demonstrates CPR and ...