FDA action counts
| Total FDA actions | 3 |
|---|---|
| Warning letters | 0 |
| Recalls | 3 |
| Approval records | 0 |
| Form 483 inspection citations | 0 |
| Most recent action | June 17, 2026 |
Risk pattern analysis
Argus HQ analysis — not an FDA finding
This section is Argus HQ analysis, not an FDA finding. Boston Scientific Neuromodulation Corporation has 3 separate FDA recalls on file, more than a single isolated recall event. A pattern across multiple FDA touchpoints does not by itself establish that any specific product currently poses a risk; it reflects only the frequency of FDA engagement with this company as recorded in Argus HQ's database. Argus HQ ingests these records directly from FDA's own public enforcement and approval databases rather than from company disclosures. This page reflects only the FDA event types Argus HQ currently tracks -- FDA Warning Letters, recalls, drug and biologic approvals, and Form 483 inspection observations -- and will update automatically as new FDA records are observed.
Enforcement history
On 2026-06-17, Argus HQ recorded a FDA recall for Boston Scientific Neuromodulation Corporation, rated "high" severity in Argus HQ's classification: Boston Scientific Neuromodulation Corporation — Class II recall: Boston Scientific CSK Electrodes: REF: CSK-TC10, CSK Electrode, STAINLESS STEEL… An FDA recall record reflects a firm removing or correcting a product already in distribution because it does not meet FDA requirements. On 2026-06-17, Argus HQ recorded a FDA recall for Boston Scientific Neuromodulation Corporation, rated "high" severity in Argus HQ's classification: Boston Scientific Neuromodulation Corporation — Class II recall: Boston Scientific TCN Electrodes: REF: TCN-5, TCN Electrode, NITINOL, 5 cm x 0.… An FDA recall record reflects a firm removing or correcting a product already in distribution because it does not meet FDA requirements. On 2026-06-17, Argus HQ recorded a FDA recall for Boston Scientific Neuromodulation Corporation, rated "high" severity in Argus HQ's classification: Boston Scientific Neuromodulation Corporation — Class II recall: Boston Scientific Model SC-4318, Clik X Anchor REF: M365SC43180 An FDA recall record reflects a firm removing or correcting a product already in distribution because it does not meet FDA requirements. In total, Boston Scientific Neuromodulation Corporation has 3 FDA events on file with Argus HQ across the sources Argus HQ currently tracks (FDA Warning Letters, recalls, drug/biologic approvals, and Form 483 inspection observations). Argus HQ ingests these records directly from FDA's own public enforcement and approval databases rather than from company disclosures. This page reflects only the FDA event types Argus HQ currently tracks -- FDA Warning Letters, recalls, drug and biologic approvals, and Form 483 inspection observations -- and will update automatically as new FDA records are observed.
Frequently asked questions
- What is the most recent FDA action on file for Boston Scientific Neuromodulation Corporation?
- June 17, 2026. Argus HQ ingests new FDA enforcement records daily.
- Has Boston Scientific Neuromodulation Corporation had product recalls?
- Yes, 3 recalls on file. See the full history below for each one.
- Is this FDA enforcement data for Boston Scientific Neuromodulation Corporation official?
- Every record links directly to its primary FDA.gov source. Argus HQ aggregates and structures public FDA data; the verbatim FDA record is always the source of truth.
- How many FDA actions has Boston Scientific Neuromodulation Corporation had?
- Argus HQ has recorded 3 FDA events for Boston Scientific Neuromodulation Corporation: 0 warning letters, 3 recalls, 0 approvals, and 0 Form 483 inspection observations. Argus HQ ingests these records directly from FDA's own public enforcement and approval databases rather than from company disclosures.
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Related enforcement actions
- Boston Scientific Neuromodulation Corporation — Class II recall: Boston Scientific CSK Electrodes: REF: CSK-TC10, CSK Electrode, STAINLESS STEEL… →
- Boston Scientific Neuromodulation Corporation — Class II recall: Boston Scientific Model SC-4318, Clik X Anchor REF: M365SC43180 →
- Boston Scientific Neuromodulation Corporation — Class II recall: Boston Scientific TCN Electrodes: REF: TCN-5, TCN Electrode, NITINOL, 5 cm x 0.… →
Compare with
- Boston Scientific Neuromodulation Corporation vs Medline Industries, LP
- Boston Scientific Neuromodulation Corporation vs ARROW INTERNATIONAL, LLC
- Boston Scientific Neuromodulation Corporation vs Stryker Sustainability Solutions
- Boston Scientific Neuromodulation Corporation vs Guardian Drug Co. Inc.
- Boston Scientific Neuromodulation Corporation vs B BRAUN MEDICAL INC
Two different companies merged onto this page by mistake? Or a name variant missing? Tell us — corrections@argushq.ai
Compiled by Argus HQ Research from FDA primary sources · Reviewed by Andy Gaber, Founder
Cite this record
Reusing this data in reporting or research? Here’s a ready-made citation.
Argus HQ Research (2026). Boston Scientific Neuromodulation Corporation's Complete FDA Record. Digital Empire LLC. Retrieved from https://argushq.ai/company/boston-scientific-neuromodulation-corporation
"Boston Scientific Neuromodulation Corporation's Complete FDA Record." Argus HQ Research, Digital Empire LLC, 2026, argushq.ai/company/boston-scientific-neuromodulation-corporation.
Argus HQ Research. "Boston Scientific Neuromodulation Corporation's Complete FDA Record." Digital Empire LLC. Accessed July 13, 2026. https://argushq.ai/company/boston-scientific-neuromodulation-corporation.
@misc{argushq_argushq_ai_company_boston_scientific_neuromodulation_corporation_2026,
title = {Boston Scientific Neuromodulation Corporation's Complete FDA Record},
author = {{Argus HQ Research}},
year = {2026},
publisher = {Digital Empire LLC},
url = {https://argushq.ai/company/boston-scientific-neuromodulation-corporation},
note = {Accessed: July 13, 2026}
}Source: FDA.gov (aggregated across Warning Letters, Recalls, Approvals, Form 483s) ↗

