FDA issues safety communication on Philips AEDs

Published on: December 11th, 2013

Certain HeartStart automated external defibrillator (AED) devices made by Philips Medical Systems, a division of Philips Healthcare, may be unable to deliver needed defibrillator shock in a cardiac emergency situation, according to a new safety communication issued by the U.S. Food and Drug Administration to users of these previously recalled devices.

Read the FDA’s noticeĀ here.

Read Philip’s notice here.

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