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 ...
The U.S. Food and Drug Administration warned Tuesday that thousands of defibrillators made by Philips Healthcare may not work during medical emergencies because of an electrical component failure in ...
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