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    Court Bars Philips From Manufacturing, Selling Some Adulterated Defibrillators

    Following its manufacture and distribution of adulterated automatic external defibrillators (AEDs) and Q-CPR meters, which the U.S. Food and Drug Administration (FDA) said put people at risk, US District Judge Denise Casper on Tuesday entered a consent decree of permanent injunction between the US and Andover, MA-based Philips North America LLC and two company officers. Under a complaint filed on behalf of FDA and alongside the consent decree, Philips was said to be...