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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 6 of 6 Results
Related Medical Device Recalls Date Classified to: 08/21/2014
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Z-0126-2010 - Medtronic Concerto, C154DWK, Dual chamber implantable cardioverter defibrillator with cardiac resynchronization therapy, atrial and ventricular therapies. Medtronic, Inc., Minneapolis, MN 55432 USA. 2 Nov-09-2009 Medtronic Inc. Cardiac Rhythm Disease Managment
Z-0127-2010 - This device is not approved in the United States. Medtronic Concerto, C174AWK. Dual Chamber implantable cardioverter defibrillator with cardiac resynchronization therapy, atrial and ventricular ther... 2 Nov-09-2009 Medtronic Inc. Cardiac Rhythm Disease Managment
Z-0131-2010 - This device is not approved in the United States. Medtronic Virtuoso VR, D164VWC. Medtronic, Inc., Minneapolis, MN 55432 USA. 2 Nov-09-2009 Medtronic Inc. Cardiac Rhythm Disease Managment
Z-0129-2010 - Medtronic Virtuoso VR, Model D154VWC, Single Chamber implantable cardioverter defibrillator with atrial therapies. Medtronic, Inc., 710 Medtronic Parkway, Minneapolis, MN 55432-5604 USA. This device i... 2 Nov-09-2009 Medtronic Inc. Cardiac Rhythm Disease Managment
Z-0130-2010 - This device is not approved in the United States. Medtronic Virtuoso DR, D164AWG. Medtronic, Inc., Minneapolis, MN 55432 USA. 2 Nov-09-2009 Medtronic Inc. Cardiac Rhythm Disease Managment
Z-0128-2010 - Medtronic Virtuoso DR, D154AWG, Dual Chamber implantable cardioverter defibrillator with atrial and ventricular therapies. Medtronic, Inc., 710 Medtronic Parkway, Minneapolis, MN 55432-5604 USA. This ... 2 Nov-09-2009 Medtronic Inc. Cardiac Rhythm Disease Managment
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