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 2023-08-02; 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: Flexiva Pulse ID 242 TracTip single Use Fiber-intended to be used as a device th…

Name: FDA Recall Record — Boston Scientific Corporation
Creator: Argus HQ
Published: 2023-08-02
License: https://argushq.ai/methodology

Event date: 2023-08-02 00:00:00Z
Observed: 2026-07-16 23:20:09Z
Source ID: Z-2234-2023
Payload hash: 82b14f296be029c503afa133…

Summary

Manufactured with the incorrect component may result in lower power output and degradation or dimming of the aiming beam, leading to reduced efficiency of fiber performance. Continued use may cause overheating of the fiber connector, which could result in a burn, if touched 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 2023-08-02; 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 (2023). Boston Scientific Corporation — Class II recall: Flexiva Pulse ID 242 TracTip single Use Fiber-intended to be used as a device th…. Digital Empire Holdings LLC. Retrieved from https://argushq.ai/events/fda-recall-boston-scientific-corporation-z-2234-2023

MLA

"Boston Scientific Corporation — Class II recall: Flexiva Pulse ID 242 TracTip single Use Fiber-intended to be used as a device th…." Argus HQ Research, Digital Empire Holdings LLC, 2023, argushq.ai/events/fda-recall-boston-scientific-corporation-z-2234-2023.

Chicago

Argus HQ Research. "Boston Scientific Corporation — Class II recall: Flexiva Pulse ID 242 TracTip single Use Fiber-intended to be used as a device th…." Digital Empire Holdings LLC. Accessed July 23, 2026. https://argushq.ai/events/fda-recall-boston-scientific-corporation-z-2234-2023.

BibTeX

@misc{argushq_argushq_ai_events_fda_recall_boston_scientific_corporation_z_2234_2023_2023,
  title = {Boston Scientific Corporation — Class II recall: Flexiva Pulse ID 242 TracTip single Use Fiber-intended to be used as a device th…},
  author = {{Argus HQ Research}},
  year = {2023},
  publisher = {Digital Empire Holdings LLC},
  url = {https://argushq.ai/events/fda-recall-boston-scientific-corporation-z-2234-2023},
  note = {Accessed: July 23, 2026}
}

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