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.
Topics: None