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 ...
SEATTLESEATTLE — Philips said Monday it is recalling about 5,400 HeartStart FR2 automated external defibrillators due to a possible memory chip failure that could make the device unable to work ...
LONDON — Koninklijke Philips Electronics NV (Amsterdam, The Netherlands), a leading vendor of consumer and medical products, has announced that it is recalling approximately 5,400 HeartStart FR2+ ...
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 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 ...
A voluntary recall has been issued on four models of defibrillators over possible voltage detector problems. The Department of Health is warning the public to be aware that the affected Philips ...
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 ...
Royal Philips Electronics (NYSE: PHG, AEX: PHI) is introducing Philips HeartStart FR3 automated external defibrillator (AED) during Arab Health, for professional responders in the region who treat ...
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