| Medtronic Sprint Quattro Secure S, model 6935. Steroid eluting, tripolar, screw-in, ventri recall (Z-0474-2011) | Medtronic Inc. Cardiac Rhythm Disease Managment | 2010-11-26 |
| Medtronic Sprint Quattro Secure, model 6947. Steroid eluting, quadripolar, screw-in, ventr recall (Z-0475-2011) | Medtronic Inc. Cardiac Rhythm Disease Managment | 2010-11-26 |
| Medtronic Dual Chamber Temporary Pacemaker, model 5388. Manufacturer: Medtronic, Inc., 710 recall (Z-0430-2011) | Medtronic Inc. Cardiac Rhythm Disease Managment | 2010-11-22 |
| Medtronic Concerto II CRT-D, model D274TRK and Model D294TRK not available in the US. Digi recall (Z-0110-2011) | Medtronic Inc. Cardiac Rhythm Disease Managment | 2010-10-21 |
| Medtronic Consulta CRT-D, model D224TRK and Model D234TRK not available in the US. Digital recall (Z-0111-2011) | Medtronic Inc. Cardiac Rhythm Disease Managment | 2010-10-21 |
| Medtronic Maximo II CRT-D, model D284TRK. Digital implantable cardioverter defibrillator w recall (Z-0112-2011) | Medtronic Inc. Cardiac Rhythm Disease Managment | 2010-10-21 |
| Medtronic Maximo II DR, model D284DRG. Digital dual chamber implantable cardioverter defib recall (Z-0113-2011) | Medtronic Inc. Cardiac Rhythm Disease Managment | 2010-10-21 |
| Medtronic Maximo II VR, model D284VRC. Digital single chamber implantable cardioverter def recall (Z-0114-2011) | Medtronic Inc. Cardiac Rhythm Disease Managment | 2010-10-21 |
| Medtronic Secura DR, model D224DRG, and model D234DRG not available in the U.S.. Digital D recall (Z-0115-2011) | Medtronic Inc. Cardiac Rhythm Disease Managment | 2010-10-21 |
| Medtronic Secura VR, model D224VRC, and model D234VRC not available in the U.S.. Digital s recall (Z-0116-2011) | Medtronic Inc. Cardiac Rhythm Disease Managment | 2010-10-21 |
| Medtronic Virtuoso II DR, model D274DRG, and model D294DRG not available in the U.S.. Digi recall (Z-0117-2011) | Medtronic Inc. Cardiac Rhythm Disease Managment | 2010-10-21 |
| Medtronic Virtuoso II VR, model D274VRC, and model D294VRC not available in the U.S.. Digi recall (Z-0118-2011) | Medtronic Inc. Cardiac Rhythm Disease Managment | 2010-10-21 |
| Medtronic Carelink Monitor Model 2490C. The Medtronic CareLink Monitor Model 2490C is desi recall (Z-2209-2010) | Medtronic Inc. Cardiac Rhythm Disease Managment | 2010-08-11 |
| Medtronic HMS PLUS, Hemostasis Management System. Medtronic, Inc., Cardiovascular Division recall (Z-1537-2010) | Medtronic Inc. Cardiac Rhythm Disease Managment | 2010-05-04 |
| Medtronic EnRhythm, P1501DR, Dual Chamber Rate Responsive Pacemaker with RapidRead Telemet recall (Z-1440-2010) | Medtronic Inc. Cardiac Rhythm Disease Managment | 2010-04-26 |
| Medtronic, Sutureless, unipolar, myocardial, screw-in pacing lead, 5071-15, 5071-25, 5071- recall (Z-1200-2010) | Medtronic Inc. Cardiac Rhythm Disease Managment | 2010-03-23 |
| Medtronic Concerto, C154DWK, Dual chamber implantable cardioverter defibrillator with card recall (Z-0126-2010) | Medtronic Inc. Cardiac Rhythm Disease Managment | 2009-11-09 |
| This device is not approved in the United States. Medtronic Concerto, C174AWK. Dual Chambe recall (Z-0127-2010) | Medtronic Inc. Cardiac Rhythm Disease Managment | 2009-11-09 |
| Medtronic Virtuoso DR, D154AWG, Dual Chamber implantable cardioverter defibrillator with a recall (Z-0128-2010) | Medtronic Inc. Cardiac Rhythm Disease Managment | 2009-11-09 |
| Medtronic Virtuoso VR, Model D154VWC, Single Chamber implantable cardioverter defibrillato recall (Z-0129-2010) | Medtronic Inc. Cardiac Rhythm Disease Managment | 2009-11-09 |
| This device is not approved in the United States. Medtronic Virtuoso DR, D164AWG. Medtroni recall (Z-0130-2010) | Medtronic Inc. Cardiac Rhythm Disease Managment | 2009-11-09 |
| This device is not approved in the United States. Medtronic Virtuoso VR, D164VWC. Medtroni recall (Z-0131-2010) | Medtronic Inc. Cardiac Rhythm Disease Managment | 2009-11-09 |
| Medtronic SIGMA 100/200/300 Series IPGs, Single Chamber Pacemaker; models SS103, SS106, SS recall (Z-1510-2009) | Medtronic Inc. Cardiac Rhythm Disease Managment | 2009-06-11 |
| Medtronic KAPPA 600/700/900 Series Implantable Pulse Generator (IPGs), Single Chamber Rate recall (Z-1511-2009) | Medtronic Inc. Cardiac Rhythm Disease Managment | 2009-06-11 |
| Medtronic SIGMA 100/200/300 Series IPGs, Single Chamber Rate Responsive Pacemaker; models recall (Z-1512-2009) | Medtronic Inc. Cardiac Rhythm Disease Managment | 2009-06-11 |
| Medtronic KAPPA 600/700/900 Series Implantable Pulse Generator (IPGs), Dual Chamber Pacema recall (Z-1513-2009) | Medtronic Inc. Cardiac Rhythm Disease Managment | 2009-06-11 |
| Medtronic SIGMA 100/200/300 Series IPGs, Dual Chamber Pacemaker, models SD203 and SD303. recall (Z-1514-2009) | Medtronic Inc. Cardiac Rhythm Disease Managment | 2009-06-11 |
| Medtronic KAPPA 600/700/900 Series Implantable Pulse Generator (IPGs), Dual Chamber Rate R recall (Z-1515-2009) | Medtronic Inc. Cardiac Rhythm Disease Managment | 2009-06-11 |
| Medtronic SIGMA 100/200/300 Series IPGs, Dual Chamber Rate Responsive Pacemaker, models DR recall (Z-1516-2009) | Medtronic Inc. Cardiac Rhythm Disease Managment | 2009-06-11 |
| Medtronic SIGMA 100/200/300 Series IPGs, Dual Chamber atrial sensing, ventricular sensing recall (Z-1517-2009) | Medtronic Inc. Cardiac Rhythm Disease Managment | 2009-06-11 |
| Medtronic SIGMA 100/200/300 Series IPGs, Single Chamber Pacemaker, model SVVI103, for vent recall (Z-1518-2009) | Medtronic Inc. Cardiac Rhythm Disease Managment | 2009-06-11 |
| Medtronic KAPPA 600/700/900 Series Implantable Pulse Generator (IPGs), Dual Chamber atrial recall (Z-1519-2009) | Medtronic Inc. Cardiac Rhythm Disease Managment | 2009-06-11 |