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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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MIRRO MRI VR SureScan, Model Number DVME3D1, Implantable Cardioverter Defibrillator
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2
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06/26/2024
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Medtronic Inc.
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MIRRO MRI VR SureScan, Model Number DVME3D4, Implantable Cardioverter Defibrillator
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2
|
06/26/2024
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Medtronic Inc.
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COBALT DR MRI SureScan, Model Number DDPB3D1, 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
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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
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06/26/2024
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Medtronic Inc.
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COBALT XT VR MRI SureScan, Model Number DVPA2D1, 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 Implantable Cardioverter Defibrillator, product number DDPA2D1
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2
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01/22/2024
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Medtronic Inc.
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ICD-DR DDBB1D1 EVERA XT IS1/DF1 US, Model Number DDBB1D1; 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-DR DDBB1D4 EVERA XT IS1/DF4 US, Model Number DDBB1D4; 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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