Recall database

Stimulator, Spinal-Cord, Totally Implanted For Pain Relief recalls

Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.

Showing 1–3 of 3 recalls

Class IOngoingZ-2879-2026

Boston Scientific Neuromodulation Corporation recalls INFINION CX LEAD KIT

Spinal cord stimulation system lead body may be exposed to stress at the anchor site. This may result in high impedance measurements or lead fractures, which may lead to inadequate stimulation, additional intervention, i…

Boston Scientific Neur…CAAug 12, 2026

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

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