PlainRecalls

Medtronic Neuromodulation

Compiled from official public sources by the publisher.

98 recalls on record · Latest: Jun 3, 2026

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Agency notice ledger

Federal filing book Medtronic Neuromodulation MID-BOOK · SINGLE-AGENCY

#171 of 14,151 · 98 notices · 0.094% archive

  • BOOK 98 notices
  • RANK #171 of 14,151
  • SHARE 0.094% archive
  • AGENCY FDA Devices (98)
  • CAT medical devices
  • CATS 1 category
  • LATEST Jun 3, 2026
  • PHOTO Advanced Pharma Inc.

Nearest notice-volume peer: Advanced Pharma Inc. (1 notice gap)

Medtronic Neuromodulation accounts for about 0.094% of the 104,423-notice archive on 98 distinct filings — a heavy share signal beside absolute volume. FDA · CPSC · USDA FSIS · NHTSA notice stamps for this firm. Read with this firm → · Dominant category → · Similar-volume firm →

Medtronic Neuromodulation's standing among 14,151 recalling firms

Medtronic Neuromodulation ranks 171st of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Medtronic Neuromodulation vs all firms by recall-notice count

Where this firm's archive sits among every tracked recalling manufacturer

98 171st of 14151 higher than 13,980 of 14,151 firms

Firms, banded by distinct federal recall-event inventory

Each bar is a band; taller bars hold more firms. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source FDA · CPSC · USDA FSIS · NHTSA federal recall filings · 2026-09-13

Medtronic Neuromodulation in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Medtronic Neuromodulation holds about 0.094% of archive notices alongside 98 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
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 CLINICIAN TABLET US, Model Number CT900A; 2. PROG CT900B CLINICIAN TABLET EU -UK, Model Number CT900B; 3. PROG CT900C CLINICIAN TABLET UK, Model Number CT900C; 4. PROG CT900D CLINICIAN TABLET GLOBAL, Model Number CT900D; 5. PROG CT900E CLINICIAN TABLET GLBL SMSNG, Model Number CT900E; 6. PROG CT900F CLINICIAN TABLET GLBL SMSNG, Model Number CT900
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 Samsung tablets (CFN CT900).
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 CT900B PROG CT900B CLINICIAN TABLET EU -UK CT900C PROG CT900C CLINICIAN TABLET UK CT900D PROG CT900D CLINICIAN TABLET GLOBAL CT900E PROG CT900E CLINICIAN TABLET GLBL SMSNG CT900F PROG CT900F CLINICIAN TABLET GLBL SMSNG
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) neurostimulators
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.x, CFN CT900D
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, CFN CT900C
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.x, CFN CT900B
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 TABLET PAPER EN with the A810 CP app version 2.x, CFN CT900E
FDA Devices Moderate Nov 20, 2024

Medtronic Recharger Kits, RS6230, RS7230, and RS5220A, containing components WR9230 and WR9220A Recharger for rechargeable implantable neurostimulators. The Rechargers are used with Neurostimulator Inceptiv INS Model 977119 and Percept RC INS Model B35300 as part of the Deep Brain Stimulation (DBS) system. WR9220A is used with InterStim Micro, Model 97810, as part of Pelvic Health system
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 TM90 Communicator.
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 2.0.4648), Version 3.0.x (3.0.1057, 3.0.1062, 3.0.1081, and 3.0.1098), Version 4.0.x (4.0.1052). Includes the below product descriptions: 1. ADAPTOR 64001 1X4 MVMT POCKET ADAPTOR, 2. ADAPTOR 64002 2X4 MVMT POCKET ADAPTOR, 3. INS 37602 Activa SC Neurostimulator, 4. INS 37603 Activa SCx Neurostimulator, 5. INS B35200 DBS PERCEPT PC,

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 deep brain stimulation
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 therapy.
FDA Devices Moderate Aug 31, 2022

Vanta Clinician Programmer Application, Model A71200. For programming of the Medtronic Model 977006 Vanta implantable neurostimulators for pain therapy.
FDA Devices Moderate Jun 1, 2022

Vanta INS Implantable Neurostimulator. Medtronic Model 977006 Vanta with AdaptiveStim Technology Neurostimulator with Surescan MRI technology, part of a neurostimulator system for pain therapy.
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) TH90QFA, 3) TH90PFA, 4) TH90GFA, 5) TG90G01; b) InterStim X Clinician Therapy Application Software, Model Number A51300; and c) InterStim x "My Therapy" Patient Therapy Application Software, Model Number A52300
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), Restore Ultra SureScan MRI (Model 97712), and RestoreSensor SureScan MRI (Model 97714) implantable neurostimulators.
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 AdaptiveStim Technology Model 97715 Implanted Neurostimulator  Intellis Model 97716 Implanted Neurostimulator.

Medtronic Neuromodulation carries an outsized archive share

Drug and device firms outside this manufacturer and state, matched by notice volume and category footprint.

Similar recall count

Nearest multi-notice firms by distinct-event totals (98 here — heavy-book).

Advanced Pharma Inc. 99 Angiodynamics, Inc. 99 Encore Medical, LP 99 Fresh Express Incorporated 99 Kenworth 99

Similar medical devices volume

Nearest multi-notice firms in the same narrow category lane.

Angiodynamics, Inc. 99 Encore Medical, LP 99 Zimmer GmbH 99 CooperSurgical, Inc. 97

Frequently Asked Questions

How many federal recall notices name Medtronic Neuromodulation? ▼
PlainRecalls indexes 98 distinct federal recall events naming Medtronic Neuromodulation, aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (archive as of September 2026). That count is an issuance inventory, not a hazard score.
Where does Medtronic Neuromodulation sit among other recalling firms? ▼
Medtronic Neuromodulation ranks #171 of 14,151 by distinct recall-event count among 14,151 firms in this archive (99th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Medtronic Neuromodulation's notices? ▼
FDA Devices accounts for 98 of this firm's 98 indexed notices.
What product category dominates Medtronic Neuromodulation's filing book? ▼
Filings for Medtronic Neuromodulation span 1 product category, led by medical devices. Browse that category archive for peer firms and related notices.
Is a higher notice count more dangerous? ▼
No. Archive size reflects how often federal agencies publish recalls naming the firm — reporting volume, coverage, and product range all move the number. Always verify the individual notice with the issuing agency before acting on a specific product.
Medtronic Neuromodulation: 98 federal recall notices aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (lead agency FDA Devices). Verify individual notices with FDA directly before acting on a specific recall.

Firm-level totals aggregate distinct federal recall events naming Medtronic Neuromodulation; individual notices remain authoritative on each linked recall page.

Methodology · Corrections · FDA · CPSC · USDA FSIS · NHTSA · Archive as of September 2026