Has Boston Scientific Neuromodulation Corporation had other FDA enforcement actions?

Yes. Argus HQ has recorded 10 total FDA actions tied to Boston Scientific Neuromodulation Corporation: 0 warning letters, 10 recalls, 0 approval records, and 0 Form 483 inspection citations.

What kind of FDA record is this?

This is an Argus HQ record of a FDA Recall, tagged high severity by Argus HQ. FDA published the underlying record on 2025-09-24; Argus observed and indexed it on 2026-07-16.

Where can I verify this record directly with FDA?

The verbatim FDA source record is the source of truth — Argus HQ links directly to it below. Always confirm against fda.gov before acting.

.hq

fda_recall · device_recall · high

Boston Scientific Neuromodulation Corporation — Class II recall: Vercise Deep Brain Stimulation Systems Surgical Implant Manual, Document Number:…

Name: FDA Recall Record — Boston Scientific Neuromodulation Corporation
Creator: Argus HQ
Published: 2025-09-24
License: https://argushq.ai/methodology

Event date: 2025-09-24 00:00:00Z
Observed: 2026-07-16 23:20:09Z
Source ID: Z-2558-2025
Payload hash: d63ee9dede4fc74164a48280…

Summary

Wire break(s) have occurred in rechargeable deep brain stimulation implantable pulse generators, implanted in the submuscular pectoral location. Wire breaks prevent successful stimulation, thus requiring device removal/replacement and users may experience high monopolar impedances, undesired sensati… Status: Ongoing.

Entities

Boston Scientific Neuromodulation Corporation

View source record ↗

Frequently asked questions

Has Boston Scientific Neuromodulation Corporation had other FDA enforcement actions?: Yes. Argus HQ has recorded 10 total FDA actions tied to Boston Scientific Neuromodulation Corporation: 0 warning letters, 10 recalls, 0 approval records, and 0 Form 483 inspection citations.
What kind of FDA record is this?: This is an Argus HQ record of a FDA Recall, tagged high severity by Argus HQ. FDA published the underlying record on 2025-09-24; Argus observed and indexed it on 2026-07-16.
Where can I verify this record directly with FDA?: The verbatim FDA source record is the source of truth — Argus HQ links directly to it below. Always confirm against fda.gov before acting.

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.

APA

Argus HQ Research (2025). Boston Scientific Neuromodulation Corporation — Class II recall: Vercise Deep Brain Stimulation Systems Surgical Implant Manual, Document Number:…. Digital Empire Holdings LLC. Retrieved from https://argushq.ai/events/fda-recall-boston-scientific-neuromodulation-corporation-z-2558-2025

MLA

"Boston Scientific Neuromodulation Corporation — Class II recall: Vercise Deep Brain Stimulation Systems Surgical Implant Manual, Document Number:…." Argus HQ Research, Digital Empire Holdings LLC, 2025, argushq.ai/events/fda-recall-boston-scientific-neuromodulation-corporation-z-2558-2025.

Chicago

Argus HQ Research. "Boston Scientific Neuromodulation Corporation — Class II recall: Vercise Deep Brain Stimulation Systems Surgical Implant Manual, Document Number:…." Digital Empire Holdings LLC. Accessed July 23, 2026. https://argushq.ai/events/fda-recall-boston-scientific-neuromodulation-corporation-z-2558-2025.

BibTeX

@misc{argushq_argushq_ai_events_fda_recall_boston_scientific_neuromodulation_corporation_z_2558_2025_2025,
  title = {Boston Scientific Neuromodulation Corporation — Class II recall: Vercise Deep Brain Stimulation Systems Surgical Implant Manual, Document Number:…},
  author = {{Argus HQ Research}},
  year = {2025},
  publisher = {Digital Empire Holdings LLC},
  url = {https://argushq.ai/events/fda-recall-boston-scientific-neuromodulation-corporation-z-2558-2025},
  note = {Accessed: July 23, 2026}
}

Informational only. Not legal, financial, or medical advice.