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U.S. Department of Health and Human Services

Medical Device Recalls

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11 to 20 of 20 Results
Recall Date to: 05/24/2015 PMA Number: P980035
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Product Description
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FDA Recall
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Medtronic SIGMA 100/200/300 Series IPGs, Single Chamber Pacemaker; models SS103, SS106, SS203, and S... 1 06/11/2009 Medtronic Inc. Cardiac Rhythm Disease Managment
Medtronic SIGMA 100/200/300 Series IPGs, Single Chamber Rate Responsive Pacemaker; models SR353, SSR... 1 06/11/2009 Medtronic Inc. Cardiac Rhythm Disease Managment
Sigma implantable pulse generators (IPGs) Single Chamber Pacemaker model SVVI103, for ventricular us... 2 02/18/2006 Medtronic Inc. Cardiac Rhythm Managment
Sigma implantable pulse generators (IPGs) Single Chamber Rate Responsive Pacemaker, models SSR203, S... 2 02/18/2006 Medtronic Inc. Cardiac Rhythm Managment
Sigma implantable pulse generators (IPGs) Single Chamber Pacemaker, models SS103, SS106, SS203, SS30... 2 02/18/2006 Medtronic Inc. Cardiac Rhythm Managment
Sigma implantable pulse generators (IPGs) Dual Chamber Atrial Sensing, Ventricular Sensing and Pacin... 2 02/18/2006 Medtronic Inc. Cardiac Rhythm Managment
Sigma implantable pulse generators (IPGs) Dual Chamber Rate Responsive Pacemaker, models SDR203, SDR... 2 02/18/2006 Medtronic Inc. Cardiac Rhythm Managment
Sigma implantable pulse generators (IPGs) dual Chamber Pacemaker, models SD203, SD303 2 02/18/2006 Medtronic Inc. Cardiac Rhythm Managment
Kappa Model 901 Implantable Pulse Generators (IPGs) are pacemaker devices that provide therapies for... 2 07/20/2004 Medtronic Inc. Cardiac Rhythm Managment
Kappa Model 701 Implantable Pulse Generators (IPGs) are pacemaker devices that provide therapies for... 2 07/20/2004 Medtronic Inc. Cardiac Rhythm Managment
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