PlainRecalls

Medtronic Neuromodulation

Compiled from official public sources by the editorial team.

98 recalls on record · Latest: Jun 3, 2026

Medtronic Neuromodulation Recall Insight

Medtronic Neuromodulation appears on 98 federal recall records indexed by PlainRecalls, out of 101,704 total recalls tracked across the FDA, CPSC, and NHTSA. That represents approximately 0.096% of the federal archive, a data point that is only interpretable alongside production volume, product mix, and decades of operation, because a high recall count alone does not establish fault. Large, diversified firms that sell tens of millions of units across many categories will mechanically accumulate more recall records than small manufacturers, even when their defect rates per unit shipped are comparable or lower. The most recent action on this firm is dated Jun 3, 2026, which is the anchor point for assessing whether enforcement is currently active or historical.

On this page of 50 entries, severity tagging shows 0 critical, 50 moderate, and 0 lower-severity recalls. Affected-unit counts are disclosed on 50 of 50 entries, unit-count disclosure is more common on CPSC and NHTSA actions and less common on FDA drug/device recalls, where lot numbers and distribution scope substitute for absolute totals. The records on this page span 1 distinct product categories, with issuing agencies dominated by FDA Devices (50). The date window on this page runs from May 12, 2021 to Jun 3, 2026.

Manufacturer-level browsing is useful when monitoring a single firm for patterns, whether recalls cluster around one product family (suggesting a specific design or supplier issue) or scatter across the firm's entire catalog (which can indicate systemic quality-control problems or deliberate regulator attention). Clicking into each recall reveals the specific hazard, remedy, and distribution scope that together determine whether a consumer is actually at risk. For decisions that depend on being current, deciding whether a product in your home is safe, whether to return a gift, or whether to accept a replacement, always verify the recall number on the issuing agency's site, because federal agencies amend, terminate, and re-scope recalls over time and only the agency's live record reflects the current legal status. This page aggregates what agencies have published publicly and is intended for consumer awareness and research.

FDA Devices Moderate Jun 3, 2026

Medtronic 1x4 Pocket Adaptor Kit for Deep Brain Stimulation, Model 64001; Stimulator, electrical, implanted, for parkinsonian tremor

FDA Devices Moderate Jun 3, 2026

Medtronic 2x4 Pocket Adaptor Kit for Deep Brain Stimulation, Model 64002; Stimulator, electrical, implanted, for parkinsonian tremor

FDA Devices Moderate May 20, 2026

Medtronic SynchroMed Flex Infusion Mode - A810 Clinician Programmer Software Application, loaded on the following devices: 1. PROG CT900A CLINICI…

FDA Devices Moderate Jan 21, 2026

A71200 Vanta" Clinician Programmer Application (CP App) version 2.0.2465 and 2.0.2683, Product number A71200. Software is deployed and operated on S…

FDA Devices Moderate Dec 31, 2025

Restore Clinician Programmer Application (CP App), Model A71100 used with the following programmers: CT900A PROG CT900A CLINICIAN TABLET US CT900…

FDA Devices Moderate May 7, 2025

Enhanced Verify Evaluation Handset (CFN HH90130FA)

FDA Devices Moderate Apr 16, 2025

Stimulation RC Clinician Programmer Application, Model A71400, when used with the Inceptiv (Model 977119) and Intellis Pro (Model 977118) neurostimul…

FDA Devices Moderate Apr 9, 2025

A820 myPTM Software Application associated with Medtronic SynchroMed Pump and Infusion System.

FDA Devices Moderate Jan 8, 2025

SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable pumps used with PROG CT900D CLINICIAN TABLET GLOBAL with the A810 CP app version 2…

FDA Devices Moderate Jan 8, 2025

SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable pumps used with PROG CT900C CLINICIAN TABLET UK with the A810 CP app version 2.x, …

FDA Devices Moderate Jan 8, 2025

SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable pumps used with PROG CT900B CLINICIAN TABLET EU -UK with the A810 CP app version 2…

FDA Devices Moderate Jan 8, 2025

SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable pumps used with PROG CT900E CLINICIAN TABLET GLBL SMSNG and PROG CT900E CLINICIAN …

FDA Devices Moderate Nov 20, 2024

Medtronic Recharger Kits, RS6230, RS7230, and RS5220A, containing components WR9230 and WR9220A Recharger for rechargeable implantable neurostimulat…

FDA Devices Moderate Oct 30, 2024

SynchroMed II Infusion Pump. Product Number: 8637-20

FDA Devices Moderate Oct 30, 2024

Medtronic Percept RC Implantable Neurostimulators (INS), Model B35300.

FDA Devices Moderate Oct 23, 2024

Vanta Implantable Neurostimulator (INS), Model 977006

FDA Devices Moderate Sep 18, 2024

Medtronic Handset with Communicator, Model TH90Q01, InterStim Smart Programmer and Communicator Kits, containing the Model HH90 Handset and the TM…

FDA Devices Moderate Jul 31, 2024

A610 Clinician Programmer (CP) Software Application (app) with the following versions: Version 2.0.x (2.0.4584, 2.0.4594, 2.0.4605, 2.0.4630, and 2.0…

FDA Devices Moderate Jul 24, 2024

Medtronic Ascenda Intrathecal Catheter, Models: a) 8780 (114 cm); b) 8781 (140 cm); c) 8784 (catheter pump revision kit)

FDA Devices Moderate May 8, 2024

Intellis AdaptiveStim Product Number 97715, Spinal Cord Stimulator

FDA Devices Moderate Jan 31, 2024

Model A710 Intellis Clinician Programmer Application, version 2.0.97

FDA Devices Moderate Jan 3, 2024

Medtronic SynchroMed II, Model 8637-20, Programmable pump

FDA Devices Moderate Jan 3, 2024

Medtronic SynchroMed II, Model 8637-40, Programmable pump

FDA Devices Moderate Nov 29, 2023

Model 97745 Controller used with Models 97715 and 97716 Intellis Neurostimulators

FDA Devices Moderate Nov 8, 2023

LEAD 3387S-40 STIMLOC DBS, Model Number 3387S-40. Electrical implantable device.

FDA Devices Moderate Oct 25, 2023

SenSight Connector Plug, Model Number B31061.

FDA Devices Moderate Oct 11, 2023

Restore Clinician Programmer Application Software, model number A71100, used with the Restore Neurostimulators.

FDA Devices Moderate Aug 16, 2023

Medtronic InterStim Ground Pad REF 041826

FDA Devices Moderate Aug 2, 2023

A901 Communication Manager Application, used in conjunction with the A710 Clinician Programmer application..

FDA Devices Moderate Jul 5, 2023

Vanta with AdaptiveStim Implantable Neurostimulator, Model 977006; spinal chord stimulation

FDA Devices Moderate Apr 26, 2023

Medtronic SenSight Extension Tunneler Kit, REF B31030; The Extension Tunneler Kit is used to assist in the tunneling and passage of extensions for de…

FDA Devices Moderate Jan 18, 2023

Vanta/Seqenita LT Clinician Programmer Application, Neurostimulation systems for pain therapy, Model Number CT900C

FDA Devices Moderate Jan 18, 2023

Vanta/Seqenita LT Clinician Programmer Application, Neurostimulation systems for pain therapy, Model Number CT900E

FDA Devices Moderate Jan 18, 2023

Vanta/Seqenita LT Clinician Programmer Application, Neurostimulation systems for pain therapy, Model Number CT900B

FDA Devices Moderate Jan 18, 2023

Vanta/Seqenita LT Clinician Programmer Application, Neurostimulation systems for pain therapy, Model Number CT900D

FDA Devices Moderate Jan 18, 2023

Vanta/Seqenita LT Clinician Programmer Application, Neurostimulation systems for pain therapy, Model Number CT900A

FDA Devices Moderate Aug 31, 2022

Vanta Clinician Programmer Application, Model A71200. For programming of the Medtronic Model 977006 Vanta implantable neurostimulators for pain ther…

FDA Devices Moderate Aug 31, 2022

Vanta Clinician Programmer Application, Model A71200. For programming of the Medtronic Model 977006 Vanta implantable neurostimulators for pain ther…

FDA Devices Moderate Jun 1, 2022

Vanta INS Implantable Neurostimulator. Medtronic Model 977006 Vanta with AdaptiveStim Technology Neurostimulator with Surescan MRI technology, part o…

FDA Devices Moderate Jun 1, 2022

Percept PC BrainSense Implantable Neurostimulator (INS) Model B35200

FDA Devices Moderate Jun 1, 2022

Percept BrainSense Implantable Neurostimulator (INS), Model B35200

FDA Devices Moderate May 4, 2022

MEDTRONIC INTERSTIM THERAPY SYSTEM FOR URINARY CONTROL, which includes the following: a) Handset with Communicator, Model Numbers: 1) TH90Q01, 2) T…

FDA Devices Moderate Jan 5, 2022

Model B35200 - Percept PC BrainSense Implantable Neurostimulator

FDA Devices Moderate Dec 1, 2021

Medtronic Wireless Recharger Model WR9200 included in the RS7200 Recharger Kit used by the RestoreUltra (Model 37712), RestoreSensor (Model 37714), R…

FDA Devices Moderate Dec 1, 2021

Medtronic Wireless Recharger Model WR9200 included in the RS6200 Recharger Kit used by the Activa RC (Model 37612) implantable neurostimulator.

FDA Devices Moderate Dec 1, 2021

Medtronic Wireless Recharger Model WR9220 included in the RS5200 Recharger Kit used by the InterStim Micro (Model 97810) implantable neurostimulator.

FDA Devices Moderate Nov 10, 2021

Clinician Programmer Application (CPA) model A610 Clinician Software Application

FDA Devices Moderate Aug 18, 2021

Medtronic StimLoc Burr Hole Cover, Part Numbers: a) 3387S-40 b) 3389S-28 c) 3389S-40 d) 3391S-40 e) 3550S-01 f) 924256 g) DB-5000

FDA Devices Moderate Aug 4, 2021

Medtronic Vectris SureScan MRI, Catalog Numbers: a) 977A260 b) 977A275 c) 977A290

FDA Devices Moderate May 12, 2021

Intellis Model 97755 Recharger - Product Usage: designed to charge the following Medtronic rechargeable neurostimulators:  Intellis with AdaptiveSti…

Nearby Manufacturers

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Data Sources

  • Source: FDA + CPSC + NHTSA - federal recall filings naming this firm. Verify with FDA, CPSC, or NHTSA directly.
  • Source: PlainRecalls Manufacturer Index - firm-level aggregation across all three federal recall feeds

Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. Recalls are aggregated across FDA, CPSC and NHTSA filings that name this firm; the total reflects the federal record, not an independent investigation. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.