Has Boston Scientific Corporation had other FDA enforcement actions?

Yes. Argus HQ has recorded 272 total FDA actions tied to Boston Scientific Corporation: 0 warning letters, 272 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 2024-04-03; 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 Corporation — Class II recall: OptiCross Coronary Imaging Catheter, REF H749518080120

Name: FDA Recall Record — Boston Scientific Corporation
Creator: Argus HQ
Published: 2024-04-03
License: https://argushq.ai/methodology

Event date: 2024-04-03 00:00:00Z
Observed: 2026-07-16 23:20:09Z
Source ID: Z-1396-2024
Payload hash: a9e498f4232394f0ab750e80…

Summary

Certain batches of Opticross 40MHz Coronary Imaging Catheters manufactured using an incorrect voltage setting, which may have resulted in decreased image brightness. Status: Ongoing.

Entities

Boston Scientific Corporation

View source record ↗

Frequently asked questions

Has Boston Scientific Corporation had other FDA enforcement actions?: Yes. Argus HQ has recorded 272 total FDA actions tied to Boston Scientific Corporation: 0 warning letters, 272 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 2024-04-03; 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 (2024). Boston Scientific Corporation — Class II recall: OptiCross Coronary Imaging Catheter, REF H749518080120. Digital Empire Holdings LLC. Retrieved from https://argushq.ai/events/fda-recall-boston-scientific-corporation-z-1396-2024

MLA

"Boston Scientific Corporation — Class II recall: OptiCross Coronary Imaging Catheter, REF H749518080120." Argus HQ Research, Digital Empire Holdings LLC, 2024, argushq.ai/events/fda-recall-boston-scientific-corporation-z-1396-2024.

Chicago

Argus HQ Research. "Boston Scientific Corporation — Class II recall: OptiCross Coronary Imaging Catheter, REF H749518080120." Digital Empire Holdings LLC. Accessed July 23, 2026. https://argushq.ai/events/fda-recall-boston-scientific-corporation-z-1396-2024.

BibTeX

@misc{argushq_argushq_ai_events_fda_recall_boston_scientific_corporation_z_1396_2024_2024,
  title = {Boston Scientific Corporation — Class II recall: OptiCross Coronary Imaging Catheter, REF H749518080120},
  author = {{Argus HQ Research}},
  year = {2024},
  publisher = {Digital Empire Holdings LLC},
  url = {https://argushq.ai/events/fda-recall-boston-scientific-corporation-z-1396-2024},
  note = {Accessed: July 23, 2026}
}

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