Recalls from Medtronic Neuromodulation

• Medtronic InterStim SureScan MRI Leads and Percutaneous Extensions (opens in a new tab)
  Moderate risk, FDA, Oct 22, 2026, Device defect
• Medtronic 1x4 and 2x4 Pocket Adaptor Kit for Deep Brain Stimulation (opens in a new tab)
  Moderate risk, FDA, May 28, 2026, Labeling error
• Medtronic SynchroMed Flex Infusion Mode - A810 Clinician Programmer Software Application (opens in a new tab)
  Moderate risk, FDA, May 14, 2026, Software defect
• Medtronic Vanta Clinician Programmer Application (opens in a new tab)
  Moderate risk, FDA, Jan 9, 2026, Device defect

Data: Recall Canary (opens in a new tab)