|
Product Description
|
Recall Class
|
FDA Recall Posting Date
|
Recalling Firm
|
Z-1767-2023 - CRTD DTMB2Q1 AMPLIA MRI QUAD OUS DF1, Model Number DTMB2Q1; Implantable Cardioverter Defibrillators
|
1
|
06/16/2023
|
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
|
Z-1766-2023 - CRTD DTMB2D4 AMPLIA MRI OUS DF4, Model Number DTMB2D4; Implantable Cardioverter Defibrillators
|
1
|
06/16/2023
|
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
|
Z-1765-2023 - CRTD DTMB2D1 AMPLIA MRI OUS DF1, Model Number DTMB2D1; Implantable Cardioverter Defibrillators
|
1
|
06/16/2023
|
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
|
Z-1764-2023 - CRTD DTMB1QQ AMPLIA MRI QUAD US DF4, Model Number DTMB1QQ; Implantable Cardioverter Defibrillators
|
1
|
06/16/2023
|
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
|
Z-1763-2023 - CRTD DTMB1Q1 AMPLIA MRI QUAD US DF1, Model Number DTMB1Q1; Implantable Cardioverter Defibrillators
|
1
|
06/16/2023
|
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
|
Z-1762-2023 - CRTD DTMB1D4 AMPLIA MRI US DF4, Model Number DTMB1D4; Implantable Cardioverter Defibrillators
|
1
|
06/16/2023
|
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
|
Z-1761-2023 - CRTD DTMB1D1 AMPLIA MRI US DF1, Model Number DTMB1D1; Implantable Cardioverter Defibrillators
|
1
|
06/16/2023
|
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
|
Z-1760-2023 - CRTD DTMA2QQ CLARIA MRI QUAD OUS DF4, Model Number DTMA2QQ; Implantable Cardioverter Defibrillators
|
1
|
06/16/2023
|
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
|
Z-1759-2023 - CRTD DTMA2Q1 CLARIA MRI QUAD OUS DF1, Model Number DTMA2Q1; Implantable Cardioverter Defibrillators
|
1
|
06/16/2023
|
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
|
Z-1758-2023 - CRTD DTMA2D4 CLARIA MRI OUS DF4, Model Number DTMA2D4; Implantable Cardioverter Defibrillators
|
1
|
06/16/2023
|
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
|