N/A 37022Recalls & reported problems
Medtronic, Inc. · ENS 37022 EXTERNAL STIM DBS EMANUAL EN · Class f
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00763000404413), received between Oct 5, 2023 and Oct 5, 2023 — classified as 1 malfunction.
The most frequently reported specific device problem is “High impedance” (1 report).
20 other recalls cover devices cleared under the same FDA submission (H020007, H050003, 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. How this data works · Data updated Oct 16, 2026.
Reports received per month
Most reported problems
Device problems
- High impedance1
- Impedance Problem1
- Insufficient Device Problem Information1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 5, 2023High impedance; Impedance Problem; Insufficient Device Problem Information; High impedance; Impedance Problem; Insufficient Device Problem Information
ADDITIONAL INFORMATION RECEIVED FROM THE MANUFACTURER¿S REPRESENTATIVE (REP) REPORTED TROUBLESHOOTING PERFORMED RELATED TO THE ISSUE INCLUDING TURNING OFF THE PATIENT PROGRAMMER WHEN OPENING ANOTHER LEAD. THE PROGRAMMER WAS TURNED BACK ON. RECONNECTION WAS ESTABLISHED AND CONNECTIVITY PASSED. IT WAS UNCLEAR IF IT WAS USING A NEW LEAD OR TURNING THE PATIENT PROGRAMMER OFF THEN BACK ON WHICH RESOLVED THE ISSUE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17882967 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under H020007, H050003, P960009. One submission often covers many models, so check the product and lot details in each record.
- Z-2240-2026 · May 13, 2026 · Open, ClassifiedMedtronic 1x4 Pocket Adaptor Kit for Deep Brain Stimulation, Model 64001; Stimulator, electrical, implanted, for parkinsonian tremor
- Z-2241-2026 · May 13, 2026 · Open, ClassifiedMedtronic 2x4 Pocket Adaptor Kit for Deep Brain Stimulation, Model 64002; Stimulator, electrical, implanted, for parkinsonian tremor
- Z-0206-2025 · Sep 24, 2024 · Open, ClassifiedMedtronic Percept RC Implantable Neurostimulators (INS), Model B35300.
- Z-0372-2025 · Sep 18, 2024 · Open, ClassifiedMedtronic 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 · CompletedLEAD 3387S-40 STIMLOC DBS, Model Number 3387S-40. Electrical implantable device.
- Z-1128-2022 · Mar 30, 2022 · Open, ClassifiedPercept BrainSense Implantable Neurostimulator (INS), Model B35200
- Z-0418-2022 · Oct 19, 2021 · Open, ClassifiedModel B35200 - Percept PC BrainSense Implantable Neurostimulator
- Z-0201-2022 · Sep 23, 2021 · Open, ClassifiedClinician Programmer Application (CPA) model A610 Clinician Software Application
- Z-1368-2021 · Mar 9, 2021 · Open, ClassifiedA610 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 · TerminatedDBS 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 · TerminatedDBS 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 · TerminatedMedtronic, Lead Kit for DBS Stimulation. Model Numbers 3387S-40 (p/n 3387S0007V) & 3389S-40 (p/n 3389S0008V).
- Z-1617-2015 · Apr 16, 2015 · TerminatedMedtronic DBS Extension Kit for Deep Brain Stimulation, Models 37085 and 37086. Sterile
- Z-0279-2014 · Sep 30, 2013 · TerminatedMedtronic 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 · TerminatedMedtronic 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.
Other Deep brain stimulator for obsessive compulsive disorder (OCD) devices
- Activa® 37602Medtronic, Inc. · Deep brain stimulator for obsessive compulsive disorder (OCD)1 recall6 deaths777 reports
- Percept™ PC BrainSense™ B35200Medtronic, Inc. · Deep brain stimulator for obsessive compulsive disorder (OCD)4 recalls1 death547 reports
- Activa® PC 37601Medtronic, Inc. · Deep brain stimulator for obsessive compulsive disorder (OCD)122 reports
- Activa® PC 37601Medtronic, Inc. · Deep brain stimulator for obsessive compulsive disorder (OCD)2 deaths115 reports
- NA 64002Medtronic, Inc. · Deep brain stimulator for obsessive compulsive disorder (OCD)1 recall2 reports
- Activa® PC 37601Medtronic, Inc. · Deep brain stimulator for obsessive compulsive disorder (OCD)21 reports
- NA 37022Medtronic, Inc. · Deep brain stimulator for obsessive compulsive disorder (OCD)20 reports
- DBS™ 3391S-40Medtronic, Inc. · Deep brain stimulator for obsessive compulsive disorder (OCD)2 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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