Medical Device Recalls
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111 to 120 of 120 Results
Related Medical Device Recalls |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Z-1814-2023 - ICD-VR DVMD3D1 PRIMO MRI, Model Number DVMD3D1; Implantable Cardioverter Defibrillators | 1 | 06/16/2023 | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) |
Z-1815-2023 - ICD-VR DVMD3D4 PRIMO MRI, Model Number DVMD3D4; Implantable Cardioverter Defibrillators | 1 | 06/16/2023 | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) |
Z-1816-2023 - ICD-VR DVME3D1 MIRRO MRI, Model Number DVME3D1; Implantable Cardioverter Defibrillators | 1 | 06/16/2023 | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) |
Z-1817-2023 - ICD-VR DVME3D4 MIRRO MRI, Model Number DVME3D4; Implantable Cardioverter Defibrillators | 1 | 06/16/2023 | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) |
Z-1818-2023 - ICD COBALT XT VR MRI IS1 DF1, Model Number DVPA2D1; Implantable Cardioverter Defibrillators | 1 | 06/16/2023 | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) |
Z-1819-2023 - ICD COBALT XT VR MRI DF4, Model Number DVPA2D4; Implantable Cardioverter Defibrillators | 1 | 06/16/2023 | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) |
Z-1820-2023 - ICD COBALT VR MRI IS1 DF1, Model Number DVPB3D1; Implantable Cardioverter Defibrillators | 1 | 06/16/2023 | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) |
Z-1821-2023 - ICD COBALT VR MRI DF4, Model Number DVPB3D4; Implantable Cardioverter Defibrillators | 1 | 06/16/2023 | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) |
Z-1822-2023 - ICD CROME VR MRI IS1 DF1, Model Number DVPC3D1; Implantable Cardioverter Defibrillators | 1 | 06/16/2023 | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) |
Z-1823-2023 - ICD CROME VR MRI DF4, Model Number DVPC3D4; Implantable Cardioverter Defibrillators | 1 | 06/16/2023 | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) |
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