N/A 97745NT (UDI 00763000700447)Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00763000700447), received between Oct 13, 2023 and Oct 13, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Charging Problem” (1 report).

9 other recalls cover devices cleared under the same FDA submission (P840001); they may or may not involve this specific model.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Most reported problems

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• MalfunctionOct 13, 2023Display or Visual Feedback Problem; Charging Problem; Display or Visual Feedback Problem; Charging Problem

  INFORMATION WAS RECEIVED FROM A MANUFACTURER'S REPRESENTATIVE (REP) REGARDING AN EXTERNAL DEVICE. THE REASON FOR CALL WAS REP CALLED WITH AN OUT OF BOX FAILURE AND REPORTS THAT ONE OF THE CONTROLLERS FROM HER TRUNK STOCK WOULD NOT TAKE A CHARGE. REP REPORTS THAT THE AC POWER CORD LIGHT WAS GREEN, AND EVEN TRIED OTHER OUTLETS AND OTHER AC POWER CORDS, BUT THE GREEN LIGHT ON THE CONTROLLER WOULD NOT TURN ON. REP REPORTS THAT SHE ALSO TRIED OTHER LI BP'S THAT HAD BEEN CHARGED IN OTHER CONTROLLERS, AND THESE WOULD ALSO NOT CHARGE AND SHOW THE GREEN LIGHT ON THE CONTROLLER. THE ISSUE WAS NOT RESOLVED THROUGH TROUBLESHOOTING. THE CALLER WAS WARM TRANSFERRED TO CUSTOMER SERVICE TO HAVE THE DEVICE REPLACED IN HER TRUNK STOCK SINCE IT WAS NOT YET ASSIGNED TOA PATIENT. (B)(6) 2023 E1 (REP): ADDITIONAL INFORMATION WAS RECEIVED FROM A MANUFACTURER REPRESENTATIVE (REP). THE REP REPORTED THAT THE DEVICE WAS RETURNED. *SEE GENERAL FOR DEVICE RETURN INFO.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17930642 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under P840001. One submission often covers many models, so check the product and lot details in each record.

• Z-0372-2025 · Sep 18, 2024 · Open, Classified
  Medtronic Recharger Kits, RS6230, RS7230, and RS5220A, containing components WR9230 and WR9220A Recharger for rechargeable implantable neurostimulators. The Rechargers are used wi
• Z-1691-2024 · Mar 28, 2024 · Open, Classified
  Intellis AdaptiveStim Product Number 97715, Spinal Cord Stimulator
• Z-0780-2024 · Dec 19, 2023 · Open, Classified
  Model A710 Intellis Clinician Programmer Application, version 2.0.97
• Z-2159-2021 · Jul 9, 2021 · Open, Classified
  Medtronic Vectris SureScan MRI, Catalog Numbers: a) 977A260 b) 977A275 c) 977A290
• Z-1926-2016 · May 3, 2016 · Terminated
  Medtronic RestoreSensor, Model 37714; and, RestoreSensor SureScan, (MRI), Model 97714, Implantable Neurostimulators. Used to treat chronic, intractable pain of the trunk and/or li
• Z-1147-2015 · Jan 9, 2015 · Terminated
  The Medtronic, Quadripolar ITREL 3 IPG, Model 7425, is a multiprogrammable device designed for use in the Stimulation of the Central Nervous System, Peripheral Nervous System, or m
• Z-1524-2014 · Feb 27, 2014 · Terminated
  Medtronic neurostimulators. Restore (37711), RestoreADVANCED (37713), RestoreADVANCED SureScan MRI (97713), RestoreSENSOR (37714), RestoreSENSOR SureScan MRI (97714), PrimeAdvanced
• Z-0278-2014 · Sep 30, 2013 · Terminated
  Medtronic RestoreUltra, model 37712, and RestoreSensor, model 37714, Multi-program Rechargeable Neurostimulator for Spinal Cord Stimulation.
• Z-1536-06 · Aug 2, 2006 · Terminated
  Medtronic 3777 Lead Kit, 1x8 Low Impedance Lead Kit for Spinal Cord Stimulation (SCS). Manufactured at: Medtronic, Inc., Villalba, Puerto Rico USA. Medtronic, Inc., Minneapolis