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 ...
Philips recalled its HeartStart MRx Defibrillator due to an equipment defect, according to a Feb. 9 safety notice from the FDA. Here are three things to know. 1. Philips initiated the recall in June ...
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 Philips HeartStart OnSite Defibrillator is lightweight and easy to use. Providers can use the product to help save the lives of co-workers or residents, the firm notes.
On November 3rd, a joint request for temporary stay was filed in the District of Massachusetts in a patent infringement case which has played out between Dutch medical electronics firm Koninklijke ...
Washington(CBS.MW) -- The Food and Drug Administration Thursday granted market clearance to Philips Medical Systems' HeartStart Home Defibrillator for use without a prescription. The action marks the ...
AMSTERDAM (Reuters) - Medical equipment maker Philips missed forecasts for fourth-quarter earnings on Tuesday and disclosed a dispute with the U.S. Justice Department over heart defibrillators it had ...
The FDA has approved an over-the-counter home defibrillator from Philips for use in emergency (or kinky sexual) situations. When the shock is delivered within five minutes of the sudden cardiac arrest ...
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