Medical Device Recalls
-
91 to 96 of 96 Results
PMA Number: P980016 |
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Medtronic Maximo II VR D284VRC, for ventricular pacing and defibrillation. | 2 | 01/28/2009 | Medtronic Inc. Cardiac Rhythm Managment |
Medtronic Maximo DR, model 7278 Single Chamber Implantable Cardioverter Defibrillator (ICD)devices a... | 2 | 03/11/2005 | Medtronic Inc. Cardiac Rhythm Managment |
Medtronic Marquis DR, model 7274 Dual Chamber Implantable Cardioverter Defibrillator (ICD) devices a... | 2 | 03/11/2005 | 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 Marquis VR, model 7230 Single Chamber Implantable Cardioverter Defibrillator (ICD)devices ... | 2 | 03/11/2005 | Medtronic Inc. Cardiac Rhythm Managment |
Medtronic GEM DR Implantable Cardioverter Defibrillators, Model 7271 | 1 | 07/20/2004 | Medtronic Inc. Cardiac Rhythm Managment |
-