Medical Device Recalls
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91 to 96 of 96 Results
Recall Date to: 07%2F14%2F2014 PMA Number: P980016 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Medtronic Maximo II DR D28DRG, for ventricular pacing and defibrillation. | 2 | 01/28/2009 | 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 DR, model 7274 Dual Chamber Implantable Cardioverter Defibrillator (ICD) devices a... | 2 | 03/11/2005 | 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 VR, model 7230 Single Chamber Implantable Cardioverter Defibrillator (ICD)devices ... | 2 | 03/11/2005 | Medtronic Inc. Cardiac Rhythm Managment |
Medtronic RV Lead Integrity Alert , Cat. # SW012, 1.0 software in EnTrust(R) (D153ATG, D153VRC, D154... | 3 | 04/08/2009 | Medtronic Inc. Cardiac Rhythm Managment |
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