Medtronic Neuromodulation recalls

16 recalls on record · latest: May 13, 2026

Official U.S. recall history for Medtronic Neuromodulation, compiled from official government records.

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Medtronic Neuromodulation recalls Medtronic 2x4 Pocket Adaptor Kit for Deep Brain Stimulation, Model 64002; Stimulator, electrical, implanted, for parkin…

May 13, 2026 · Medical device recalls Moderate risk A limited number of Pocket Adaptor Kits, Model 64001 and 64002, are labeled wit…

Medtronic Neuromodulation recalls Medtronic 1x4 Pocket Adaptor Kit for Deep Brain Stimulation, Model 64001; Stimulator, electrical, implanted, for parkin…

May 13, 2026 · Medical device recalls Moderate risk A limited number of Pocket Adaptor Kits, Model 64001 and 64002, are labeled wit…

Medtronic Neuromodulation recalls Medtronic SynchroMed Flex Infusion Mode - A810 Clinician Programmer Software Application, loaded on the following devic…

April 8, 2026 · Medical device recalls Moderate risk Software issue: When programming the SynchroMed Pump with the A810 CP App in Fl…

Medtronic Neuromodulation recalls A71200 Vanta" Clinician Programmer Application (CP App) version 2.0.2465 and 2.0.2683, Product number A71200. Software…

December 3, 2025 · Medical device recalls Moderate risk Complaints received that Vanta A71200 CP App does not function as intended duri…

Medtronic Neuromodulation recalls Restore Clinician Programmer Application (CP App), Model A71100 used with the following programmers: CT900A PROG CT900A…

November 20, 2025 · Medical device recalls Moderate risk Software issue where a Device Reset message displayed on the app was unable to…

Medtronic Neuromodulation recalls Enhanced Verify Evaluation Handset (CFN HH90130FA)

April 3, 2025 · Medical device recalls Moderate risk Evaluation handsets may not be able to communicate with the neurostimulator due…

Medtronic Neuromodulation recalls Stimulation RC Clinician Programmer Application, Model A71400, when used with the Inceptiv (Model 977119) and Intellis…

March 4, 2025 · Medical device recalls Moderate risk There is a software issue that can permanently disable communication with an im…

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

January 9, 2025 · Medical device recalls Moderate risk Product complaints were received describing the A820 myPTM app taking longer th…

Medtronic Neuromodulation recalls SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable pumps used with PROG CT900E CLINICIAN TABLET GLBL SM…

November 21, 2024 · Medical device recalls Moderate risk Software issues were identified in application version 2.x.

Medtronic Neuromodulation recalls SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable pumps used with PROG CT900B CLINICIAN TABLET EU -UK…

November 21, 2024 · Medical device recalls Moderate risk Software issues were identified in application version 2.x.

Medtronic Neuromodulation recalls SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable pumps used with PROG CT900C CLINICIAN TABLET UK with…

November 21, 2024 · Medical device recalls Moderate risk Software issues were identified in application version 2.x.

Medtronic Neuromodulation recalls SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable pumps used with PROG CT900D CLINICIAN TABLET GLOBAL…

November 21, 2024 · Medical device recalls Moderate risk Software issues were identified in application version 2.x.

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

September 24, 2024 · Medical device recalls Moderate risk A limited number of Percept RC Implantable Neurostimulators (INS), Model B35300…

Medtronic Neuromodulation recalls Medtronic Recharger Kits, RS6230, RS7230, and RS5220A, containing components WR9230 and WR9220A Recharger for rechargea…

September 18, 2024 · Medical device recalls Moderate risk The Wireless Rechargers in the kits may be unable to enter a recharging session…

Medtronic Neuromodulation recalls SynchroMed II Infusion Pump. Product Number: 8637-20

September 11, 2024 · Medical device recalls Moderate risk Potential for error and inability to interrogate pump due to data corruption in…

Medtronic Neuromodulation recalls Vanta Implantable Neurostimulator (INS), Model 977006

August 21, 2024 · Medical device recalls Moderate risk Model 977006 Vanta INS batterty life has depleted faster than HCPs or patients…