A number of Philips ($PHG) automated external defibrillators may still be duds, potentially failing to deliver the shock needed in an emergency despite a recall ...
A faulty electronic component in some Philips HeartStart automated external defibrillators may prevent the device from delivering a needed shock to a person suffering a cardiac emergency, the FDA ...
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 ...
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 ...
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+ ...
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 ...
* Sees EBITA hit of 20 mln euros in Q4, 60 mln euros in 2018 * Latest in a series of disputes with U.S. regulators (Updates with CEO comments, background, shares) By Toby Sterling AMSTERDAM, Oct 11 ...
Health technology company Philips is suspending the manufacture of some defibrillators in the US and will make others under heightened scrutiny following criticisms from US regulators. The Dutch ...
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