Fresh Recalls

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

Boston Scientific CSK Electrodes (1)Boston Scientific Model SC-4318 (1)Boston Scientific TCN Electrodes (1)INFINION CX LEAD KIT (1)Intracept Access Instruments (1)

All Boston Scientific Neuromodulation recalls

FDA Class I · Medical device · August 12, 2026

INFINION CX LEAD KIT recall — Boston Scientific Neuromodulation Corporation

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

Intracept Access Instruments recall — Boston Scientific Neuromodulation Corporation

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

Boston Scientific Model SC-4318 recall — Boston Scientific Neuromodulation Corporation

Sterile anchors my lack sterility assurance.

Official ID Z-2404-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Boston Scientific TCN Electrodes recall — Boston Scientific Neuromodulation Corporation

Reusable electrodes may not meet expected performance levels.

Official ID Z-2403-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Boston Scientific CSK Electrodes recall — Boston Scientific Neuromodulation Corporation

Reusable electrodes may not meet expected performance levels.

Official ID Z-2402-2026 · Official record ↗

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Compiled from official public-domain government data. Last checked September 7, 2026 at 6:00 AM UTC.