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 critical severity by Argus HQ. FDA published the underlying record on 2025-01-22; 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 · critical

Boston Scientific Corporation — Class I recall: PROPONENT DR Pacemaker, SL (Model Number L201), (VDD) SL (Model Number L209), SL…

Name: FDA Recall Record — Boston Scientific Corporation
Creator: Argus HQ
Published: 2025-01-22
License: https://argushq.ai/methodology

Event date: 2025-01-22 00:00:00Z
Observed: 2026-07-16 23:20:09Z
Source ID: Z-0823-2025
Payload hash: 07c7ea2c72c87ba40760fc79…

Summary

A subset of devices from the ACCOLADE Family of Pacemakers and CRT-Ps, built before September 2018, have an increased potential to initiate Safety Mode during telemetry or other normal, higher-power operations due to latent high battery impedance. 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 critical severity by Argus HQ. FDA published the underlying record on 2025-01-22; 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 Corporation — Class I recall: PROPONENT DR Pacemaker, SL (Model Number L201), (VDD) SL (Model Number L209), SL…. Digital Empire Holdings LLC. Retrieved from https://argushq.ai/events/fda-recall-boston-scientific-corporation-z-0823-2025

MLA

"Boston Scientific Corporation — Class I recall: PROPONENT DR Pacemaker, SL (Model Number L201), (VDD) SL (Model Number L209), SL…." Argus HQ Research, Digital Empire Holdings LLC, 2025, argushq.ai/events/fda-recall-boston-scientific-corporation-z-0823-2025.

Chicago

Argus HQ Research. "Boston Scientific Corporation — Class I recall: PROPONENT DR Pacemaker, SL (Model Number L201), (VDD) SL (Model Number L209), SL…." Digital Empire Holdings LLC. Accessed July 23, 2026. https://argushq.ai/events/fda-recall-boston-scientific-corporation-z-0823-2025.

BibTeX

@misc{argushq_argushq_ai_events_fda_recall_boston_scientific_corporation_z_0823_2025_2025,
  title = {Boston Scientific Corporation — Class I recall: PROPONENT DR Pacemaker, SL (Model Number L201), (VDD) SL (Model Number L209), SL…},
  author = {{Argus HQ Research}},
  year = {2025},
  publisher = {Digital Empire Holdings LLC},
  url = {https://argushq.ai/events/fda-recall-boston-scientific-corporation-z-0823-2025},
  note = {Accessed: July 23, 2026}
}

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