Medtronic Neuromodulation: Medical Device Recalls in 2023

According to to data from the FDA, there were 13 medical device recalls made by Medtronic Neuromodulation in 2023. See the details of the recalls below.

You can see similar recalls for other firms.

• Vanta/Seqenita LT Clinician Programmer Application, Neurostimulation systems for pain therapy, Model Number CT900C
• Vanta/Seqenita LT Clinician Programmer Application, Neurostimulation systems for pain therapy, Model Number CT900B
• Vanta/Seqenita LT Clinician Programmer Application, Neurostimulation systems for pain therapy, Model Number CT900A
• Vanta/Seqenita LT Clinician Programmer Application, Neurostimulation systems for pain therapy, Model Number CT900D
• Vanta/Seqenita LT Clinician Programmer Application, Neurostimulation systems for pain therapy, Model Number CT900E
• Medtronic InterStim Ground Pad REF 041826
• SenSight Connector Plug, Model Number B31061.
• Model 97745 Controller used with Models 97715 and 97716 Intellis Neurostimulators
• Vanta with AdaptiveStim Implantable Neurostimulator, Model 977006; spinal chord stimulation
• Medtronic SenSight Extension Tunneler Kit, REF B31030; The Extension Tunneler Kit is used to assist in the tunneling and passage of extensions for deep brain stimulation
• A901 Communication Manager Application, used in conjunction with the A710 Clinician Programmer application..
• LEAD 3387S-40 STIMLOC DBS, Model Number 3387S-40. Electrical implantable device.
• Restore Clinician Programmer Application Software, model number A71100, used with the Restore Neurostimulators.