Medical Device Recalls
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1 to 3 of 3 Results
Related Medical Device Recalls Recall Date to: 04/20/2014 |
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Product Description
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Recall
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FDA Recall
Posting Date |
Recalling Firm
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Z-1249-2012 - Medtronic EnTrust, Single Chamber Implantable, Cardioverter Defibrillator with Ventricular Therapies, models D153VRC and D154VRC. The implantable cardioverter defibrillator is intended to provide ven... | 2 | 03/22/2012 | Medtronic Inc. Cardiac Rhythm Disease Management |
Z-1250-2012 - Medtronic EnTrust, Dual Chamber Implantable, Cardioverter Defibrillator with Ventricular Therapies, models D153DRG and D154DRG. The implantable cardioverter defibrillator is intended to provide ventr... | 2 | 03/22/2012 | Medtronic Inc. Cardiac Rhythm Disease Management |
Z-1248-2012 - Medtronic EnTrust, Dual Chamber Implantable, Cardioverter Defibrillator with Atrial and Ventricular Therapies, models D153ATG and D154ATG. The device is indicated for use in ICD patients with atrial ... | 2 | 03/22/2012 | Medtronic Inc. Cardiac Rhythm Disease Management |
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