Medtronic Neuromodulation: Medical Device Recalls in 2022

According to to data from the FDA, there were 7 medical device recalls made by Medtronic Neuromodulation in 2022. See the details of the recalls below.

You can see similar recalls for other firms.

• Percept PC BrainSense Implantable Neurostimulator (INS) Model B35200
• Percept BrainSense Implantable Neurostimulator (INS), Model B35200
• MEDTRONIC INTERSTIM THERAPY SYSTEM FOR URINARY CONTROL, which includes the following: a) Handset with Communicator, Model Numbers: 1) TH90Q01, 2) TH90QFA, 3) TH90PFA, 4) TH90GFA, 5) TG90G01; b) InterStim X Clinician Therapy Application Software, Model Number A51300; and c) InterStim x "My Therapy" Patient Therapy Application Software, Model Number A52300
• Vanta Clinician Programmer Application, Model A71200. For programming of the Medtronic Model 977006 Vanta implantable neurostimulators for pain therapy.
• Model B35200 - Percept PC BrainSense Implantable Neurostimulator
• Vanta Clinician Programmer Application, Model A71200. For programming of the Medtronic Model 977006 Vanta implantable neurostimulators for pain therapy.
• Vanta INS Implantable Neurostimulator. Medtronic Model 977006 Vanta with AdaptiveStim Technology Neurostimulator with Surescan MRI technology, part of a neurostimulator system for pain therapy.