Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of MedtronicLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Medtronic Neuromodulation with 100 device recalls. The most recent is a device recall dated Sep 8, 2026: InterStim Percutaneous Extensions EXT 3560022 ISTM II PERC 3560022 EXT 356003….
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Sep 8, 2026 | InterStim Percutaneous Extensions EXT 3560022 ISTM II PERC 3560022 EXT 3560030 ISTM MICRO PERC 3560030Class II · Wrong lead or percutaneous extension selected. Use of an incompatible lead or percutaneous extension will prevent the sy | Device recalls |
| Sep 8, 2026 | InterStim SureScan MRI Leads 978A1 & 978B1: LEAD 978A128 ISTM MICRO 28CM SSMRI TINED 978A128 LEAD 978A133 ISTM MICRO 33CM SSMRI TINEDClass II · Wrong lead or percutaneous extension selected. Use of an incompatible lead or percutaneous extension will prevent the sy | Device recalls |
| May 13, 2026 | Medtronic 1x4 Pocket Adaptor Kit for Deep Brain Stimulation, Model 64001; Stimulator, electrical, implanted, for parkinsonian tremorClass II · A limited number of Pocket Adaptor Kits, Model 64001 and 64002, are labeled with incorrect Use-By-Dates. | Device recalls |
| May 13, 2026 | Medtronic 2x4 Pocket Adaptor Kit for Deep Brain Stimulation, Model 64002; Stimulator, electrical, implanted, for parkinsonian tremorClass II · A limited number of Pocket Adaptor Kits, Model 64001 and 64002, are labeled with incorrect Use-By-Dates. | Device recalls |
| Apr 8, 2026 | Medtronic SynchroMed Flex Infusion Mode - A810 Clinician Programmer Software Application, loaded on the following devices: 1. PROG CT900Class II · Software issue: When programming the SynchroMed Pump with the A810 CP App in Flex Infusion Mode, the infusion steps sho | Device recalls |
| Dec 3, 2025 | A71200 Vanta" Clinician Programmer Application (CP App) version 2.0.2465 and 2.0.2683, Product number A71200. Software is deployed and operClass II · Complaints received that Vanta A71200 CP App does not function as intended during use. There is a potential for prolonge | Device recalls |
| Nov 20, 2025 | Restore Clinician Programmer Application (CP App), Model A71100 used with the following programmers: CT900A PROG CT900A CLINICIAN TABLET Class II · Software issue where a Device Reset message displayed on the app was unable to be cleared. In rare cases, this resulted | Device recalls |
| Apr 3, 2025 | Enhanced Verify Evaluation Handset (CFN HH90130FA)Class II · Evaluation handsets may not be able to communicate with the neurostimulator due to handsets having a faster processing s | Device recalls |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
