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 ...
WASHINGTON – Federal health regulators are warning the public that certain cardiac defibrillators recalled by Philips Healthcare may fail to deliver a needed shock in an emergency. Defibrillators are ...
The North American subsidiary of Amsterdam-based Royal Philips reached an agreement on a consent decree with the U.S. Department of Justice, representing the Food and Drug Administration, the company ...
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+ ...
AMSTERDAM (Reuters) - Health technology company Philips is suspending the manufacture of some defibrillators in the United States and will make others under heightened scrutiny following criticisms ...
The FINANCIAL — 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 ...
ANDOVER, Mass., Oct. 3 (UPI) -- Philips says it is recalling some automated-external defibrillators due to a possible malfunction that could keep them from analyzing heart rhythms properly. The ...
SEATTLESEATTLE — Philips Healthcare said Saturday it is recalling about 5,400 automated external defibrillators after receiving reports of a memory chip failure in a small number of some models that ...
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