Medical Device Recalls
-
91 to 96 of 96 Results
PMA Number: P980016 |
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
ICD COBALT XT VR MRI DF4, Model Number DVPA2D4; Implantable Cardioverter Defibrillators | 1 | 06/16/2023 | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) |
ICD COBALT VR MRI IS1 DF1, Model Number DVPB3D1; Implantable Cardioverter Defibrillators | 1 | 06/16/2023 | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) |
ICD COBALT VR MRI DF4, Model Number DVPB3D4; Implantable Cardioverter Defibrillators | 1 | 06/16/2023 | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) |
ICD CROME VR MRI IS1 DF1, Model Number DVPC3D1; Implantable Cardioverter Defibrillators | 1 | 06/16/2023 | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) |
ICD CROME VR MRI DF4, Model Number DVPC3D4; Implantable Cardioverter Defibrillators | 1 | 06/16/2023 | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) |
Cobalt XT DR MRI SureScan Implantable Cardioverter Defibrillator, product number DDPA2D1 | 2 | 01/22/2024 | Medtronic Inc. |
-