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automated external defibrillators Blogs and DiscussionsArticles

 
Defibtech Lifeline and ReviveR Automated External Defibrillators (AEDs): Recall - Software Defect May Cancel Shock by FDA [Posted 05/10/2011] AUDIENCE: Emergency Medicine, Risk Manager ISSUE: Devices subject to this recall include Model DDU-100 series with software version 2.004 or earlier, sold under the brand names L
Philips HeartStart FRx, HeartStart HS1 Home, and HeartStart HS1 OnSite Automated External Defibrillators (AED) by FDA In September 2012, Philips Healthcare initiated a Voluntary Medical Device Recall of HeartStart Frx, HeartStart HS1 Home, and HeartStart HS1 OnSite AEDs after determining that an internal electrical component in the AED coul
FDA issues proposal to improve the quality of automated external defibrillators by FDA The U.S. Food and Drug Administration today issued a proposed order aimed at helping manufacturers improve the quality and reliability of automated external defibrillators (AEDs).
FDA Says Build a Better External Defibrillator And Starts a Program-Too Many Recalls by Medical Quack Patient ExpertHealth Maven to strengthen automated external defibrillators, or AEDs.  They are the lifesaving devices used to treat sudden cardiac arrest. The FDA plan, dubbed the "External Defibrillator Improvement Initiative", aims to improve...
Good point about having automate ... by Medical Quack Patient ExpertHealth Maven way to speed up response times, Chan suggests, is to make automated external defibrillators, or AEDs... Good point about having automated defibrillators at the hospital...they are are airports...
Medtronic to Recall External Defibrillators by Medical Quack Patient ExpertHealth Maven a type of external defibrillator subject to a recent recall could cause serious injury or death... with its Lifepack 15 heart defibrillators that can cause a loss of power. The problem only affects devices...
LIFEPAK 20 and LIFEPAK 20e External Defibrillator/Monitors by Physio-Control Inc.: Class I Recall Due To Power Supply Failure by FDA AC power". A failure of DC (battery) power can result in the inability to deliver defibrillation.... BACKGROUND: The LIFEPAK 20 and LIFEPAK 20e defibrillator/monitor is designed for use by trained medical...
Class I Medical Device Recall: Physio-Control Inc., LIFEPAK 20 and LIFEPAK 20e External Defibrillator/Monitors by FDA Product(s): LIFEPAK 20 and LIFEPAK 20e External Defibrillator/Monitors Physio-Control notification..., 2002 to September 19, 2007.  Use: The LIFEPAK 20 and LIFEPAK 20e defibrillator/monitor is designed...
Ladies of the night to use AEDs by Dr. Ivor K. Medical Doctor to do something about it. They want to get trained in CPR, as well as equip their work place with automated external defibrillators..., and is able to treat them through defibrillation, the application of electrical therapy which stops...
Defibtech Announces a Voluntary Recall of DDU-100 series AEDs by FDA is initiating a worldwide voluntary recall of certain DDU-100 series semi-automatic external defibrillators...

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Treatment If you suspect either yourself, or someone you know, is having a heart attack, d ... » Read on
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