If you still own one of these devices, contact Philips Healthcare for a replacement AED unit. In North America, you can call 1-800-263-3342 or email [email protected].

SEATTLE -- 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 properly.

The FDA warns that thousands of Philips automated external defibrillators (AED) might not be able to deliver a needed shock in a cardiac emergency situation.

Royal Philips Electronics, a pioneer in developing treatments to combat sudden cardiac arrest, and Air France-KLM Group, one of the leading European air transport group, today announced an agreement ...

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 FINANCIAL -- Amsterdam, the Netherlands and Vail, CO - Royal Philips, a global leader in health technology, today announced ...

A number of Philips automated external defibrillators may still be duds, potentially failing to deliver the shock needed in an emergency despite a recall initiated more than a year ago intended to ...

Philips is parting ways with its worldwide emergency care business, including its catalog of automated external defibrillators and ... with a base of more than 3 million installed AEDs and ...

Once completed, Amazon supplied them with automated external defibrillators (AEDs) manufactured by the Dutch company Koninklijke Philips NV. AEDs are specifically designed to be used with minimal ...

The Philips Emergency Care Business operates in over 130 countries and has a significant installed base of over three million ...