Has Becton Dickinson & Company had other FDA enforcement actions?

Yes. Argus HQ has recorded 96 total FDA actions tied to Becton Dickinson & Company: 0 warning letters, 96 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 2024-10-02; 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

Becton Dickinson & Co. — Class II recall: BD Phoenix M50 instrument -Intended for the rapid identification (ID) and antimi…

Name: FDA Recall Record — Becton Dickinson & Company
Creator: Argus HQ
Published: 2024-10-02
License: https://argushq.ai/methodology

Event date: 2024-10-02 00:00:00Z
Observed: 2026-07-16 23:20:09Z
Source ID: Z-3246-2024
Payload hash: 2c0a05d8d654635a52eeed58…

Summary

Escherichia coli (E. coli) misidentification for clinical samples that were tested on BD Phoenix" M50 instrument and BD Phoenix" 100, may lead to misdiagnosis and inappropriate treatment of infections caused by E. coli, 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 96 total FDA actions tied to Becton Dickinson & Company: 0 warning letters, 96 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 2024-10-02; 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 (2024). Becton Dickinson & Co. — Class II recall: BD Phoenix M50 instrument -Intended for the rapid identification (ID) and antimi…. Digital Empire Holdings LLC. Retrieved from https://argushq.ai/events/fda-recall-becton-dickinson-and-co-z-3246-2024

MLA

"Becton Dickinson & Co. — Class II recall: BD Phoenix M50 instrument -Intended for the rapid identification (ID) and antimi…." Argus HQ Research, Digital Empire Holdings LLC, 2024, argushq.ai/events/fda-recall-becton-dickinson-and-co-z-3246-2024.

Chicago

Argus HQ Research. "Becton Dickinson & Co. — Class II recall: BD Phoenix M50 instrument -Intended for the rapid identification (ID) and antimi…." Digital Empire Holdings LLC. Accessed July 23, 2026. https://argushq.ai/events/fda-recall-becton-dickinson-and-co-z-3246-2024.

BibTeX

@misc{argushq_argushq_ai_events_fda_recall_becton_dickinson_and_co_z_3246_2024_2024,
  title = {Becton Dickinson & Co. — Class II recall: BD Phoenix M50 instrument -Intended for the rapid identification (ID) and antimi…},
  author = {{Argus HQ Research}},
  year = {2024},
  publisher = {Digital Empire Holdings LLC},
  url = {https://argushq.ai/events/fda-recall-becton-dickinson-and-co-z-3246-2024},
  note = {Accessed: July 23, 2026}
}

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