Has Becton Dickinson & Company had other FDA enforcement actions?

Yes. Argus HQ has recorded 82 total FDA actions tied to Becton Dickinson & Company: 0 warning letters, 82 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 2024-12-11; 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

Becton Dickinson & Co. — Class II recall: BD COR GX Instrument Version or Model: 443990 Catalog Number: 443990

Name: FDA Recall Record — Becton Dickinson & Company
Creator: Argus HQ
Published: 2024-12-11
License: https://argushq.ai/methodology

Event date: 2024-12-11 00:00:00Z
Observed: 2026-07-16 23:20:09Z
Source ID: Z-0589-2025
Payload hash: 8c8732b314b473134e199d98…

Summary

BD confirmed that product service credentials used by some BD technical support teams to access certain BD products were accessed by an unauthorized actor. Until these product service credentials are updated, there is a risk of unauthorized access that may impact the confidentiality, integrity and/o… Status: Ongoing.

Entities

Becton Dickinson & Company

View source record ↗

Frequently asked questions

Has Becton Dickinson & Company had other FDA enforcement actions?: Yes. Argus HQ has recorded 82 total FDA actions tied to Becton Dickinson & Company: 0 warning letters, 82 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 2024-12-11; 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). Becton Dickinson & Co. — Class II recall: BD COR GX Instrument  Version or Model: 443990  Catalog Number: 443990. Digital Empire LLC. Retrieved from https://argushq.ai/events/fda-recall-becton-dickinson-and-co-z-0589-2025

MLA

"Becton Dickinson & Co. — Class II recall: BD COR GX Instrument  Version or Model: 443990  Catalog Number: 443990." Argus HQ Research, Digital Empire LLC, 2024, argushq.ai/events/fda-recall-becton-dickinson-and-co-z-0589-2025.

Chicago

Argus HQ Research. "Becton Dickinson & Co. — Class II recall: BD COR GX Instrument  Version or Model: 443990  Catalog Number: 443990." Digital Empire LLC. Accessed July 17, 2026. https://argushq.ai/events/fda-recall-becton-dickinson-and-co-z-0589-2025.

BibTeX

@misc{argushq_argushq_ai_events_fda_recall_becton_dickinson_and_co_z_0589_2025_2024,
  title = {Becton Dickinson & Co. — Class II recall: BD COR GX Instrument  Version or Model: 443990  Catalog Number: 443990},
  author = {{Argus HQ Research}},
  year = {2024},
  publisher = {Digital Empire LLC},
  url = {https://argushq.ai/events/fda-recall-becton-dickinson-and-co-z-0589-2025},
  note = {Accessed: July 17, 2026}
}

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