Medical Device Recalls
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61 to 70 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-1726-2023 - ICD COBALT DR MRI IS1 DF4, Model Number DDPB3D4; 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-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-1721-2023 - ICD COBALT XT DR MRI IS1 DF1, Model Number DDPA2D1; Implantable Cardioverter Defibrillators | 1 | 06/16/2023 | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) |
Z-1723-2023 - ICD COBALT XT DR MRI IS1 DF4, Model Number DDPA2D4; Implantable Cardioverter Defibrillators | 1 | 06/16/2023 | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) |
Z-1780-2023 - ICD COBALT XT HF QUAD OUS, Model Number DTPA2QQG; 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-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-1727-2023 - ICD CROME DR MRI IS1 DF1, Model Number DDPC3D1; Implantable Cardioverter Defibrillators | 1 | 06/16/2023 | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) |
Z-1728-2023 - ICD CROME DR MRI IS1 DF4, Model Number DDPC3D4; Implantable Cardioverter Defibrillators | 1 | 06/16/2023 | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) |
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