Medical Device Recalls
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81 to 90 of 120 Results
Related Medical Device Recalls |
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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| Z-1784-2023 - CRTD COBALT HF QUAD MRI IS4 DF4, Model Number DTPB2QQ ; Implantable Cardioverter Defibrillators | 1 | 06/16/2023 |
FEI # 2182208 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) |
| Z-1785-2023 - CRTD CROME HF MRI IS1 DF1, Model Number DTPC2D1; Implantable Cardioverter Defibrillators | 1 | 06/16/2023 |
FEI # 2182208 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) |
| Z-1786-2023 - CRTD CROME HF MRI IS1 DF4, Model Number DTPC2D4; Implantable Cardioverter Defibrillators | 1 | 06/16/2023 |
FEI # 2182208 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) |
| Z-1787-2023 - CRTD CROME HF QUAD MRI IS4 DF1, Model Number DTPC2Q1; Implantable Cardioverter Defibrillators | 1 | 06/16/2023 |
FEI # 2182208 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) |
| Z-1788-2023 - CRTD CROME HF QUAD MRI IS4 DF4, Model Number DTPC2QQ; Implantable Cardioverter Defibrillators | 1 | 06/16/2023 |
FEI # 2182208 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) |
| Z-1789-2023 - ICD-VR DVAB1D1 VISIA AF US IS1/DF1, Model Number DVAB1D1; Implantable Cardioverter Defibrillators | 1 | 06/16/2023 |
FEI # 2182208 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) |
| Z-1790-2023 - ICD-VR DVAB1D4 VISIA AF US DF4, Model Number DVAB1D4; Implantable Cardioverter Defibrillators | 1 | 06/16/2023 |
FEI # 2182208 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) |
| Z-1791-2023 - ICD-VR VISIA AF XT OUS IS1/DF1, Model Number DVAB2D1; Implantable Cardioverter Defibrillators | 1 | 06/16/2023 |
FEI # 2182208 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) |
| Z-1792-2023 - ICD-VR VISIA AF XT OUS DF4, Model Number DDVAB2D4; Implantable Cardioverter Defibrillators | 1 | 06/16/2023 |
FEI # 2182208 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) |
| Z-1793-2023 - ICD-VR VISIA AF S US/OUS IS1/DF1, Model Number DVAC3D1; Implantable Cardioverter Defibrillators | 1 | 06/16/2023 |
FEI # 2182208 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) |
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