Has Boston Scientific Corporation had other FDA enforcement actions?

Yes. Argus HQ has recorded 282 total FDA actions tied to Boston Scientific Corporation: 0 warning letters, 282 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 2026-07-29; Argus observed and indexed it on 2026-08-04.

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: FARADRIVE Steerable Sheath Clear IDE, used to facilitate access to the vasculatu…

Name: FDA Recall Record — Boston Scientific Corporation
Creator: Argus HQ
Published: 2026-07-29
License: https://argushq.ai/methodology

Event date: 2026-07-29 00:00:00Z
Observed: 2026-08-04 04:20:55Z
Source ID: Z-2754-2026
Payload hash: 06e2858aa5600bf2f3c2deeb…

Summary

Boston Scientific's complaint investigations have identified that a subset of air ingress complaints are associated with hemostatic valve damage related to dilator insertion orientation during device preparation. Valve damage may result in air ingress, potential air embolism, and associated patient… 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 282 total FDA actions tied to Boston Scientific Corporation: 0 warning letters, 282 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 2026-07-29; Argus observed and indexed it on 2026-08-04.
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 (2026). Boston Scientific Corporation — Class II recall: FARADRIVE Steerable Sheath Clear IDE, used to facilitate access to the vasculatu…. Digital Empire Holdings LLC. Retrieved from https://argushq.ai/events/fda-recall-boston-scientific-corporation-z-2754-2026

MLA

"Boston Scientific Corporation — Class II recall: FARADRIVE Steerable Sheath Clear IDE, used to facilitate access to the vasculatu…." Argus HQ Research, Digital Empire Holdings LLC, 2026, argushq.ai/events/fda-recall-boston-scientific-corporation-z-2754-2026.

Chicago

Argus HQ Research. "Boston Scientific Corporation — Class II recall: FARADRIVE Steerable Sheath Clear IDE, used to facilitate access to the vasculatu…." Digital Empire Holdings LLC. Accessed August 4, 2026. https://argushq.ai/events/fda-recall-boston-scientific-corporation-z-2754-2026.

BibTeX

@misc{argushq_argushq_ai_events_fda_recall_boston_scientific_corporation_z_2754_2026_2026,
  title = {Boston Scientific Corporation — Class II recall: FARADRIVE Steerable Sheath Clear IDE, used to facilitate access to the vasculatu…},
  author = {{Argus HQ Research}},
  year = {2026},
  publisher = {Digital Empire Holdings LLC},
  url = {https://argushq.ai/events/fda-recall-boston-scientific-corporation-z-2754-2026},
  note = {Accessed: August 4, 2026}
}

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