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NA 37651 (UDI 00613994852731)Recalls & reported problems

Medtronic, Inc. · PRGM 37651 DBS ACTIVA RC W/UPDATES US · Class 3

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00613994852731), received between Apr 6, 2023 and Apr 6, 2023 — classified as 1 injury.

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

20 other recalls cover devices cleared under the same FDA submission (P960009); 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

Device problems

  • Insufficient Device Problem Information1
  • Overheating of Device1

Patient problems

  • Burn(s)1

Recent adverse event reports

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

  • InjuryApr 6, 2023Overheating of Device; Insufficient Device Problem Information; Overheating of Device; Insufficient Device Problem Information

    IT WAS REPORTED THAT THE PATIENT RECHARGER IS PUTTING OUT TO MUCH ELECTRICITY AND WHEN THEY TRIED TO RECHARGE THEIR IMPLANT, THEY WERE BURNED TO THE POINT WHERE THEY HAVE A BURN MARK FROM THE RECHARGER ANTENNA. THE PATIENT STATED THAT THE PATIENT RECHARGER JUST STARTED DOING THIS. PATIENT DID CONFIRM THAT THERE IS NO PHYSICAL DAMAGE TO THE PATIENT RECHARGER OR THE RECHARGER ANTENNA. IMPLANT  BATTERY LEVEL WAS CHECKED WITH THE PATIENT PROGRAMMER AND WAS AT 50%. A REPLACEMENT RECHARGER WAS SENT. THE PATIENT WILL BE UPGRADED TO THE WIRELESS RECHARGER.

    Patient problems: Burn(s)

    MAUDE report 16688738 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under P960009. One submission often covers many models, so check the product and lot details in each record.

  • Z-2241-2026 · May 13, 2026 · Open, Classified
    Medtronic 2x4 Pocket Adaptor Kit for Deep Brain Stimulation, Model 64002; Stimulator, electrical, implanted, for parkinsonian tremor
  • Z-2240-2026 · May 13, 2026 · Open, Classified
    Medtronic 1x4 Pocket Adaptor Kit for Deep Brain Stimulation, Model 64001; Stimulator, electrical, implanted, for parkinsonian tremor
  • Z-0206-2025 · Sep 24, 2024 · Open, Classified
    Medtronic Percept RC Implantable Neurostimulators (INS), Model B35300.
  • 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-0217-2024 · May 27, 2022 · Completed
    LEAD 3387S-40 STIMLOC DBS, Model Number 3387S-40. Electrical implantable device.
  • Z-1128-2022 · Mar 30, 2022 · Open, Classified
    Percept BrainSense Implantable Neurostimulator (INS), Model B35200
  • Z-0418-2022 · Oct 19, 2021 · Open, Classified
    Model B35200 - Percept PC BrainSense Implantable Neurostimulator
  • Z-0201-2022 · Sep 23, 2021 · Open, Classified
    Clinician Programmer Application (CPA) model A610 Clinician Software Application
  • Z-1368-2021 · Mar 9, 2021 · Open, Classified
    A610 Clinician Programmer Application for Deep Brain Stimulation Clinician Programming Guide Percept PC Model B35200 Neurostimulator Application, version 2.0.4584, 2.0.4594, 2.0.46
  • Z-3069-2017 · Mar 17, 2017 · Terminated
    DBS Lead Depth Stop contained in Medtronic Deep Brain Stimulation (DBS) lead kits, models 3387/3387S, 3389/3389S, and 3391/3391S, The lead kit contains one DBS lead in addition to
  • Z-2645-2016 · Jun 23, 2016 · Terminated
    DBS Pocket Adaptor, Model 64001 and Model 64002. The Medtronic Models 64001 (1x4) and 64002 (2x4) Pocket Adaptors can be used as a part of a neurostimulation system for deep brain
  • Z-2602-2016 · Jun 10, 2016 · Terminated
    Medtronic, Lead Kit for DBS Stimulation. Model Numbers 3387S-40 (p/n 3387S0007V) & 3389S-40 (p/n 3389S0008V).
  • Z-1617-2015 · Apr 16, 2015 · Terminated
    Medtronic DBS Extension Kit for Deep Brain Stimulation, Models 37085 and 37086. Sterile
  • Z-0279-2014 · Sep 30, 2013 · Terminated
    Medtronic Activa PC, model 37601, and Activa RC, model 37612, Activa SC, models 37602 and 37603. Multi-program Rechargeable Neurostimulator for Deep Brain Stimulation.
  • Z-1190-2013 · Feb 8, 2013 · Terminated
    Medtronic DBS Lead Kit for Deep Brain Stimulation, models 3387, 3387S, 3389, 3389S, 3391, 3391S. Sterile and Non-Pyrogenic. Product Usage: The deep brain stimulation system del

…and 5 more.

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Sources and updates

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