Class IIOngoingZ-2404-2026
Boston Scientific Neuromodulation Corporation recalls Boston Scientific Model SC-4318
Sterile anchors my lack sterility assurance.
Boston Scientific Neur…CAJun 17, 2026
Stimulator, Spinal-Cord, Totally Implanted For Pain Relief recalls
Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 1–5 of 5 recalls
Class IIOngoingZ-1043-2026
Medtronic Neuromodulation recalls A71200 Vanta" Clinician Programmer Application (CP App) version 2.0.2465 and 2.0.2683
Complaints received that Vanta A71200 CP App does not function as intended during use. There is a potential for prolonged or postponed surgical procedure.
Medtronic Neuromodulat…MNJan 21, 2026
Class IIOngoingZ-0996-2026
Medtronic Neuromodulation recalls Restore Clinician Programmer Application (CP App)
Software issue where a Device Reset message displayed on the app was unable to be cleared. In rare cases, this resulted in an inability to resume therapy, and the patient experienced a recurrence of underlying pain sympt…
Medtronic Neuromodulat…MNDec 31, 2025
Class IIOngoingZ-0458-2026
Abbott Medical recalls Eterna SCS IPG (Implantable Pulse Generator)
There is a potential issue affecting Eterna Spinal Cord Stimulation (SCS) Implantable Pulse Generators (IPGs), Model 32400 and Liberta RC Deep Brain Stimulation (DBS) Implantable Pulse Generators (IPGs), Model 62400 .…
Abbott MedicalTXNov 19, 2025
Class IIOngoingZ-1543-2025
Medtronic Neuromodulation recalls Stimulation RC Clinician Programmer Application
There is a software issue that can permanently disable communication with an implantable neurostimulator (INS) when a specific intraoperative programming sequence is used.
Medtronic Neuromodulat…MNApr 16, 2025