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Product Description
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Recall Class
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FDA Recall Posting Date
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Recalling Firm
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COBALT DR MRI SureScan, Model Number DDPB3D1, Implantable Cardioverter Defibrillator
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2
|
06/26/2024
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Medtronic Inc.
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CROME VR MRI SureScan, Model Number DVPC3D1, Implantable Cardioverter Defibrillator
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2
|
06/26/2024
|
Medtronic Inc.
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COBALT DR MRI SureScan, Model Number DDPB3D4, Implantable Cardioverter Defibrillator
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2
|
06/26/2024
|
Medtronic Inc.
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COBALT VR MRI SureScan, Model Number DVPB3D4, Implantable Cardioverter Defibrillator
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2
|
06/26/2024
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Medtronic Inc.
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Cobalt XT DR MRI SureScan, Model Number DDPA2D1, Implantable Cardioverter Defibrillator
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2
|
06/26/2024
|
Medtronic Inc.
|
COBALT XT VR MRI SureScan, Model Number DVPA2D1, Implantable Cardioverter Defibrillator
|
2
|
06/26/2024
|
Medtronic Inc.
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Cobalt XT DR MRI SureScan Implantable Cardioverter Defibrillator, product number DDPA2D1
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2
|
01/22/2024
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Medtronic Inc.
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ICD CROME DR MRI IS1 DF4, Model Number DDPC3D4; Implantable Cardioverter Defibrillators
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1
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06/16/2023
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Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
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ICD COBALT XT VR MRI DF4, Model Number DVPA2D4; Implantable Cardioverter Defibrillators
|
1
|
06/16/2023
|
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
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ICD COBALT VR MRI IS1 DF1, Model Number DVPB3D1; Implantable Cardioverter Defibrillators
|
1
|
06/16/2023
|
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
|