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U.S. Department of Health and Human Services

Medical Device Recalls

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91 to 96 of 96 Results
Recall Date to: 07%2F14%2F2014 PMA Number: P980016
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Product Description
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Medtronic Secura VR, model D224VRC, and model D234VRC not available in the U.S.. Digital single cha... 2 10/21/2010 Medtronic Inc. Cardiac Rhythm Disease Managment
Medtronic Virtuoso DR, D154AWG, Dual Chamber implantable cardioverter defibrillator with atrial and ... 2 11/09/2009 Medtronic Inc. Cardiac Rhythm Disease Managment
Medtronic Virtuoso DR, Model D154AWG, Dual Chamber implantable cardioverter defibrillator with atria... 2 08/18/2009 Medtronic Inc. Cardiac Rhythm Managment
Medtronic Virtuoso VR, Model D154VWC, Single Chamber implantable cardioverter defibrillator with atr... 2 08/18/2009 Medtronic Inc. Cardiac Rhythm Managment
Medtronic Virtuoso VR, Model D154VWC, Single Chamber implantable cardioverter defibrillator with atr... 2 11/09/2009 Medtronic Inc. Cardiac Rhythm Disease Managment
Medtronic, Evera Implantable Cardioverter Defibrillators: Product Model EVERA XT DDBB1D1... 2 08/25/2016 Medtronic Inc., Cardiac Rhythm and Heart Failure
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