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Defibtech Lifeline and ReviveR Automated
(AEDs): Recall - Software Defect May Cancel Shock
[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
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
The U.S. Food and Drug Administration today issued a proposed order aimed at helping manufacturers improve the quality and reliability of automated
FDA Says Build a Better
And Starts a Program-Too Many Recalls
to strengthen automated
, or AEDs. They are the lifesaving devices used to treat sudden cardiac arrest. The FDA plan, dubbed the "
Improvement Initiative", aims to improve...
Medtronic to Recall
a type of
subject to a recent recall could cause serious injury or death... with its Lifepack 15 heart
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LIFEPAK 20 and LIFEPAK 20e
/Monitors by Physio-Control Inc.: Class I Recall Due To Power Supply Failure
AC power". A failure of DC (battery) power can result in the inability to deliver
.... BACKGROUND: The LIFEPAK 20 and LIFEPAK 20e
/monitor is designed for use by trained medical...
Class I Medical Device Recall: Physio-Control Inc., LIFEPAK 20 and LIFEPAK 20e
Product(s): LIFEPAK 20 and LIFEPAK 20e
/Monitors Physio-Control notification..., 2002 to September 19, 2007. Use: The LIFEPAK 20 and LIFEPAK 20e
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Class I Medical Device Recall: Defibtech LLC, DBP-2800 Battery Pack for ReviveR AED? and Lifeline AED® Semi-
(s): DBP-2800 Battery Pack for the Defibtech ReviveR AED™ and Lifeline AED® semi-
... condition, cancel charge and not provide therapy. Use: The intended use for the semi-
May Save Lives In Public Places!
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Prevent SCD with SCD ! (Subcutaneous
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