Medical Device Recalls
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71 to 80 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-1774-2023 - CRTD COBALT XT HF MRI IS1 DF1, Model Number DTPA2D1; Implantable Cardioverter Defibrillators | 1 | 06/16/2023 |
FEI # 2182208 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) |
| Z-1775-2023 - CRTD DTPA2D1G COBALT XT HF QUAD OUS, Model Number DTPA2D1G; Implantable Cardioverter Defibrillators | 1 | 06/16/2023 |
FEI # 2182208 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) |
| Z-1776-2023 - CRTD DTPA2D1PX COBALT XT HF QUAD OUS, Model Number DTPA2D1PX; Implantable Cardioverter Defibrillators | 1 | 06/16/2023 |
FEI # 2182208 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) |
| Z-1777-2023 - CRTD COBALT XT HF MRI IS1 DF4, Model Number DTPA2D4; Implantable Cardioverter Defibrillators | 1 | 06/16/2023 |
FEI # 2182208 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) |
| Z-1778-2023 - CRTD COBALT XT HF QUAD MRI IS4 DF1, Model Number DTPA2Q1; Implantable Cardioverter Defibrillators | 1 | 06/16/2023 |
FEI # 2182208 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) |
| Z-1779-2023 - CRTD COBALT XT HF QUAD MRI IS4 DF4, Model Number DTPA2QQ; Implantable Cardioverter Defibrillators | 1 | 06/16/2023 |
FEI # 2182208 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 |
FEI # 2182208 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) |
| Z-1781-2023 - CRTD COBALT HF MRI IS1 DF1, Model Number DTPB2D1; Implantable Cardioverter Defibrillators | 1 | 06/16/2023 |
FEI # 2182208 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) |
| Z-1782-2023 - CRTD COBALT HF MRI IS1 DF4, Model Number DTPB2D4; Implantable Cardioverter Defibrillators | 1 | 06/16/2023 |
FEI # 2182208 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) |
| Z-1783-2023 - CRTD COBALT HF QUAD MRI IS4 DF1, Model Number DTPB2Q1 ; Implantable Cardioverter Defibrillators | 1 | 06/16/2023 |
FEI # 2182208 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) |
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