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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 20 Results
Recall Date to: 07/31/2015 PMA Number: P980035
 
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Medtronic, Kappa 600 KDR600,KDR601,KDR603,KDR606,KDR651,KDR653 The devices are implantable pulse... 2 04/29/2011 Medtronic Inc. Cardiac Rhythm Disease Management
Medtronic EnRhythm, P1501DR, Dual Chamber Rate Responsive Pacemaker with RapidRead Telemetry. The ... 2 04/26/2010 Medtronic Inc. Cardiac Rhythm Disease Managment
Medtronic KAPPA 600/700/900 Series Implantable Pulse Generator (IPGs), Single Chamber Rate Responsiv... 1 06/11/2009 Medtronic Inc. Cardiac Rhythm Disease Managment
Medtronic KAPPA 600/700/900 Series Implantable Pulse Generator (IPGs), Dual Chamber atrial sensing, ... 1 06/11/2009 Medtronic Inc. Cardiac Rhythm Disease Managment
Medtronic SIGMA 100/200/300 Series IPGs, Single Chamber Pacemaker, model SVVI103, for ventricular us... 1 06/11/2009 Medtronic Inc. Cardiac Rhythm Disease Managment
Medtronic SIGMA 100/200/300 Series IPGs, Dual Chamber atrial sensing, ventricular sensing and pacing... 1 06/11/2009 Medtronic Inc. Cardiac Rhythm Disease Managment
Medtronic SIGMA 100/200/300 Series IPGs, Dual Chamber Rate Responsive Pacemaker, models DR353, SDR20... 1 06/11/2009 Medtronic Inc. Cardiac Rhythm Disease Managment
Medtronic KAPPA 600/700/900 Series Implantable Pulse Generator (IPGs), Dual Chamber Rate Responsive ... 1 06/11/2009 Medtronic Inc. Cardiac Rhythm Disease Managment
Medtronic SIGMA 100/200/300 Series IPGs, Dual Chamber Pacemaker, models SD203 and SD303. 1 06/11/2009 Medtronic Inc. Cardiac Rhythm Disease Managment
Medtronic KAPPA 600/700/900 Series Implantable Pulse Generator (IPGs), Dual Chamber Pacemaker, model... 1 06/11/2009 Medtronic Inc. Cardiac Rhythm Disease Managment
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