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Boston Scientific Neuromodulation Corporation: official recall notices
5 official recall or safety notices published on this site name Boston Scientific Neuromodulation Corporation, dated between 2024-07-17 and 2026-09-30. They were issued by 1 authority: US FDA — Medical Devices (5).
Countries where the notices were issued: United States (5).
Notices by year
| Year | Notices |
|---|---|
| 2026 | 2 |
| 2025 | 2 |
| 2024 | 1 |
Notices by authority
| Authority | Notices |
|---|---|
| US FDA — Medical Devices | 5 |
All notices
| Date | Authority | Product | Hazard (as classified) |
|---|---|---|---|
| 2026-09-30 | US FDA — Medical Devices | Nalu TD2 Therapy Disc with firmware, REF: 34014-001, and TD2 Patient Kit, REF: 74011, part of the Nalu Neurostimulation | — |
| 2026-06-17 | US FDA — Medical Devices | INFINION CX LEAD KIT, 50CM, Model: SC-2317-50, Material: M365SC2317500; INFINION CX LEAD KIT, 70CM, Model: SC-2317-70, | — |
| 2025-07-08 | US FDA — Medical Devices | Burr Hole Cover Kit, REF: M365DB4600C0; Burr Hole Cover Spares Kit, REF: M365DB4605C0. Components of Vercise Deep Stimu | — |
| 2025-07-08 | US FDA — Medical Devices | Vercise Deep Brain Stimulation Systems Surgical Implant Manual, Document Number: 92328632-09 | — |
| 2024-07-17 | US FDA — Medical Devices | WAVEWRITER ALPHA: Model: SC-1216, 16 IPG KIT, REF: M365SC12160; Model: SC-1232, 32 IPG KIT, REF: M365SC12320 | — |