Boston Scientific Neuromodulation recalls

4 recent recalls on record for Boston Scientific Neuromodulation in CPSC, NHTSA, and FDA data as of July 24, 2026 at 1:09 AM UTC.

Models with recalls

Boston Scientific CSK Electrodes (1)Boston Scientific Model SC-4318 (1)Boston Scientific TCN Electrodes (1)Intracept Access Instruments (1)

All Boston Scientific Neuromodulation recalls

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 ↗

Verify with the official sources:

CPSC — consumer products ↗ (aggregated here)
NHTSA — vehicles, car seats, tires ↗ (aggregated here; use NHTSA's VIN lookup to check a specific vehicle)
FDA — food, drugs, medical devices ↗ (aggregated here)
USDA FSIS — meat, poultry & egg products ↗ (not yet aggregated here)
Recalls.gov — the U.S. government’s all-agency portal ↗

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Compiled from official public-domain government data. Last checked July 24, 2026 at 1:09 AM UTC.