Medtronic Neuromodulation: 54 recalls on record

Recalls filed with 1 agency: FDA (54).

First recall on record: December 19, 2012. Most recent: June 3, 2026.

Risk classification: Class I: 14 · Class II: 39 · Class III: 1

Most recent recalls

DateAgencyProduct
June 3, 2026FDAMedtronic 2x4 Pocket Adaptor Kit for Deep Brain Stimulation, Model 64002; Stimulator, ele…Z-2241-2026
June 3, 2026FDAMedtronic 1x4 Pocket Adaptor Kit for Deep Brain Stimulation, Model 64001; Stimulator, ele…Z-2240-2026
May 20, 2026FDAMedtronic SynchroMed Flex Infusion Mode - A810 Clinician Programmer Software Application,…Z-2201-2026
December 31, 2025FDARestore Clinician Programmer Application (CP App), Model A71100 used with the following p…Z-0996-2026
January 8, 2025FDASynchroMed II Model 8637 and SynchroMed III Model 8667 implantable pumps used with PROG C…Z-0773-2025
November 20, 2024FDAMedtronic Recharger Kits, RS6230, RS7230, and RS5220A, containing components WR9230 and …Z-0372-2025
October 30, 2024FDAMedtronic Percept RC Implantable Neurostimulators (INS), Model B35300.Z-0206-2025
October 30, 2024FDASynchroMed II Infusion Pump. Product Number: 8637-20Z-0137-2025
October 23, 2024FDAVanta Implantable Neurostimulator (INS), Model 977006Z-0132-2025
September 18, 2024FDAMedtronic Handset with Communicator, Model TH90Q01, InterStim Smart Programmer and Commu…Z-3073-2024
July 31, 2024FDAA610 Clinician Programmer (CP) Software Application (app) with the following versions: Ve…Z-2427-2024
July 24, 2024FDAMedtronic Ascenda Intrathecal Catheter, Models: a) 8780 (114 cm); b) 8781 (140 cm); …Z-2352-2024
May 8, 2024FDAIntellis AdaptiveStim Product Number 97715, Spinal Cord StimulatorZ-1691-2024
January 31, 2024FDAModel A710 Intellis Clinician Programmer Application, version 2.0.97Z-0780-2024
January 3, 2024FDAMedtronic SynchroMed II, Model 8637-20, Programmable pumpZ-0614-2024
January 3, 2024FDAMedtronic SynchroMed II, Model 8637-40, Programmable pumpZ-0615-2024
June 1, 2022FDAVanta INS Implantable Neurostimulator. Medtronic Model 977006 Vanta with AdaptiveStim Tec…Z-1123-2022
August 4, 2021FDAMedtronic Vectris SureScan MRI, Catalog Numbers: a) 977A260 b) 977A275 c) 977A290Z-2159-2021
December 11, 2019FDASynchromed II programmable pump, Model numbers 8637-20 and 8637-40Z-0508-2020
July 25, 2018FDAVectris(TM) Trial Screening Lead Kit for Spinal Cord Stimulation, Models: (a) 977D160 (…Z-2431-2018
March 14, 2018FDAMedtronic Synchromed II Model 8637 supplied in 20mL and 40 mL reservoir size and a cathet…Z-0896-2018
February 14, 2018FDAMedtronic Ascenda(R) Intrathecal Catheter, Models: (a) 8780, UDI: 00643169202122, 00643…Z-0537-2018
August 30, 2017FDADBS Lead Depth Stop contained in Medtronic Deep Brain Stimulation (DBS) lead kits, models…Z-3069-2017
March 8, 2017FDAMedtronic SynchroMed II Implantable Drug Infusion System. This system includes: Model 8…Z-0788-2017
April 6, 2016FDAMedtronic, Model 8781 Ascenda" Intrathecal Catheter kit, Rx Only, Sterile Ethylene Oxide.Z-1271-2016

Questions about this company

How many recalls does Medtronic Neuromodulation have?
Recalert has 54 U.S. recalls on record for Medtronic Neuromodulation, published between December 19, 2012 and June 3, 2026.
What was the most recent Medtronic Neuromodulation recall?
FDA recall Z-2241-2026, published June 3, 2026: Medtronic 2x4 Pocket Adaptor Kit for Deep Brain Stimulation, Model 64002; Stimulator, electrical, implanted, for parkinsonian tremor
Which agencies have handled Medtronic Neuromodulation recalls?
Medtronic Neuromodulation appears as the recalling firm in recalls from: FDA (54).

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