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Guidant Brand Defibrillator Recall

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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...
Defibtech Lifeline and ReviveR Automated External Defibrillators (AEDs): Recall - Software Defect May Cancel Shock by FDA : Devices subject to this recall include Model DDU-100 series with software version 2.004 or earlier, sold under the brand names Lifeline and ReviveR. AEDs using software version 2.004 or earlier may cause the device...
Abbott Diabetes Care Recalls Tons of Glucose Test Strips–The US Has the FDA Recall Blues-Solution Has Been Touted Here for by Medical Quack Patient ExpertHealth Maven of test strips being recalled are sold under the following brand names: Precision Xceed Pro... and I’m up to around 60 posts on the topic now, and just about every time there’s a recall...
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... FDA posts press releases and other notices of recalls and market withdrawals...
Health Headlines - June 18 by Meredy Registered NurseHealth Maven Guidant Recalls 38,000 Heart Defibrillators The U.S. Food and Drug Administration and Guidant... said. Defibrillators shock an irregularly beating heart back into a normal rhythm. Guidant models recalled include...
FDA Plans Recall Data Base – Nice Still Need Tags on the Products So We Can Find Them Immediately by Medical Quack Patient ExpertHealth Maven to find recalled products, drugs, devices etc. right on the shelves.  Now with this data base... download while I’m shopping?  Duh? Recalls of both medical devices and drugs are growing...
Health Headlines - July 3 by Meredy Registered NurseHealth Maven that the system is broken," a spokesman said in a prepared statement. Some Defibrillator Recalls Classified as Most Serious The U.S. Food and Drug Administration has applied its most serious recall rating to two Guidant...
Health Headlines - January 29 by Meredy Registered NurseHealth Maven with faulty defibrillators. In the last six months, Guidant has recalled or issued safety advisories... Company Recalls 500,000 Baby Teethers At least a half million liquid-filled baby teethers...
Health Headlines - December 27 by Meredy Registered NurseHealth Maven Defibrillator Maker Gets FDA Warning Guidant, the maker of implantable heart defibrillators... had said then that it had answered the concerns. Since June, Guidant has recalled or issued warnings for about 88,000 heart...
Health Headlines - April 7 by Meredy Registered NurseHealth Maven such as implantable defibrillators, a move partly prompted by criticism of the agency's past monitoring... manufacturers and will advise the agency on how best to respond to recalls and other problems, the Times...

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