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 ...

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+ ...

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 ...

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 ...

In a bid to protect the Los Angeles public from preventable death related to sudden cardiac arrest, Philips has launched an extensive program to provide public access to automated external ...

Emirates Airline has placed a further order for the Philips Automated External Defibrillator (AED) device, FR2 AED, for the new fleet of Emirates planes that have already been ordered from Boeing and ...