Medical Device Recalls
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111 to 120 of 120 Results
Recall Date from: 06/14/2023 Recall Date to: 06/22/2023 Firm: medtronic |
Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| ICD-VR DVMD3D1 PRIMO MRI, Model Number DVMD3D1; Implantable Cardioverter Defibrillators | 1 | 06/16/2023 |
FEI # 2182208 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) |
| ICD-VR DVMD3D4 PRIMO MRI, Model Number DVMD3D4; Implantable Cardioverter Defibrillators | 1 | 06/16/2023 |
FEI # 2182208 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) |
| ICD-VR DVME3D1 MIRRO MRI, Model Number DVME3D1; Implantable Cardioverter Defibrillators | 1 | 06/16/2023 |
FEI # 2182208 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) |
| ICD-VR DVME3D4 MIRRO MRI, Model Number DVME3D4; Implantable Cardioverter Defibrillators | 1 | 06/16/2023 |
FEI # 2182208 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) |
| ICD COBALT XT VR MRI IS1 DF1, Model Number DVPA2D1; Implantable Cardioverter Defibrillators | 1 | 06/16/2023 |
FEI # 2182208 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) |
| ICD COBALT XT VR MRI DF4, Model Number DVPA2D4; Implantable Cardioverter Defibrillators | 1 | 06/16/2023 |
FEI # 2182208 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) |
| ICD COBALT VR MRI IS1 DF1, Model Number DVPB3D1; Implantable Cardioverter Defibrillators | 1 | 06/16/2023 |
FEI # 2182208 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) |
| ICD COBALT VR MRI DF4, Model Number DVPB3D4; Implantable Cardioverter Defibrillators | 1 | 06/16/2023 |
FEI # 2182208 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) |
| ICD CROME VR MRI IS1 DF1, Model Number DVPC3D1; Implantable Cardioverter Defibrillators | 1 | 06/16/2023 |
FEI # 2182208 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) |
| ICD CROME VR MRI DF4, Model Number DVPC3D4; Implantable Cardioverter Defibrillators | 1 | 06/16/2023 |
FEI # 2182208 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) |
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