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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 19 Results
Recall Date to: 07/22/2014 PMA Number: P980016
 
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Medtronic Virtuoso VR, Model D154VWC, Single Chamber implantable cardioverter defibrillator with atr... 2 11/09/2009 Medtronic Inc. Cardiac Rhythm Disease Managment
Medtronic Virtuoso VR, Model D154VWC, Single Chamber implantable cardioverter defibrillator with atr... 2 08/18/2009 Medtronic Inc. Cardiac Rhythm Managment
Medtronic Virtuoso DR, Model D154AWG, Dual Chamber implantable cardioverter defibrillator with atria... 2 08/18/2009 Medtronic Inc. Cardiac Rhythm Managment
Medtronic Virtuoso DR, D154AWG, Dual Chamber implantable cardioverter defibrillator with atrial and ... 2 11/09/2009 Medtronic Inc. Cardiac Rhythm Disease Managment
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 Secura DR, model D224DRG, and model D234DRG not available in the U.S.. Digital Dual chamb... 2 10/21/2010 Medtronic Inc. Cardiac Rhythm Disease Managment
Medtronic RV Lead Integrity Alert , Cat. # SW012, 1.0 software in EnTrust(R) (D153ATG, D153VRC, D154... 3 04/08/2009 Medtronic Inc. Cardiac Rhythm Managment
Medtronic Maximo VR, model 7232 Single Chamber Implantable Cardioverter Defibrillator (ICD)devices a... 2 03/11/2005 Medtronic Inc. Cardiac Rhythm Managment
Medtronic Maximo II VR, model D284VRC. Digital single chamber implantable cardioverter defibrillato... 2 10/21/2010 Medtronic Inc. Cardiac Rhythm Disease Managment
Medtronic Maximo II VR D284VRC, for ventricular pacing and defibrillation. 2 01/28/2009 Medtronic Inc. Cardiac Rhythm Managment
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