Boston Scientific Neuromodulation recalls
5 recent recalls on record for Boston Scientific Neuromodulation in connected official government data as of September 7, 2026 at 6:00 AM UTC.
Models with recalls
All Boston Scientific Neuromodulation recalls
FDA Class I · Medical device · August 12, 2026
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…
Official ID Z-2879-2026 ·
Official record ↗
FDA Class II · Medical device · July 15, 2026
Intraosseous nerve ablation system instruments may have sterile barrier breach of the outer tray seal, which may introduce a risk of sterility breach, and if breached could lead to…
Official ID Z-2694-2026 ·
Official record ↗
FDA Class II · Medical device · June 17, 2026
Sterile anchors my lack sterility assurance.
Official ID Z-2404-2026 ·
Official record ↗
FDA Class II · Medical device · June 17, 2026
Reusable electrodes may not meet expected performance levels.
Official ID Z-2403-2026 ·
Official record ↗
FDA Class II · Medical device · June 17, 2026
Reusable electrodes may not meet expected performance levels.
Official ID Z-2402-2026 ·
Official record ↗
Compiled from official public-domain government data. Last checked September 7, 2026 at 6:00 AM UTC.