Medical Device Recalls
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1 to 3 of 3 Results
PMA Number: P980016/S046 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Medtronic EnTrust, Single Chamber Implantable, Cardioverter Defibrillator with Ventricular Therapies... | 2 | 03/22/2012 |
FEI # 2182208 Medtronic Inc. Cardiac Rhythm Disease Management |
| Medtronic EnTrust, Dual Chamber Implantable, Cardioverter Defibrillator with Ventricular Therapies, ... | 2 | 03/22/2012 |
FEI # 2182208 Medtronic Inc. Cardiac Rhythm Disease Management |
| Medtronic EnTrust, Dual Chamber Implantable, Cardioverter Defibrillator with Atrial and Ventricular ... | 2 | 03/22/2012 |
FEI # 2182208 Medtronic Inc. Cardiac Rhythm Disease Management |
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