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 2025-11-19; 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 Kiestra" Isolate Suspension Cuvette Array; Catalog No.: 246100;

Name: FDA Recall Record — Becton Dickinson & Company
Creator: Argus HQ
Published: 2025-11-19
License: https://argushq.ai/methodology

Event date: 2025-11-19 00:00:00Z
Observed: 2026-07-16 23:20:09Z
Source ID: Z-0484-2026
Payload hash: bc68a0aa35a349ec27f051d9…

Summary

The 2D barcodes on these cuvettes contain formatting errors that prevent the analyzing system from correctly reading the expiration date. As a result, the instrument enters an error state and the cuvettes cannot be used. 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 2025-11-19; 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). Becton Dickinson & Co. — Class II recall: BD Kiestra" Isolate Suspension Cuvette Array;  Catalog No.: 246100;. Digital Empire Holdings LLC. Retrieved from https://argushq.ai/events/fda-recall-becton-dickinson-and-co-z-0484-2026

MLA

"Becton Dickinson & Co. — Class II recall: BD Kiestra" Isolate Suspension Cuvette Array;  Catalog No.: 246100;." Argus HQ Research, Digital Empire Holdings LLC, 2025, argushq.ai/events/fda-recall-becton-dickinson-and-co-z-0484-2026.

Chicago

Argus HQ Research. "Becton Dickinson & Co. — Class II recall: BD Kiestra" Isolate Suspension Cuvette Array;  Catalog No.: 246100;." Digital Empire Holdings LLC. Accessed July 23, 2026. https://argushq.ai/events/fda-recall-becton-dickinson-and-co-z-0484-2026.

BibTeX

@misc{argushq_argushq_ai_events_fda_recall_becton_dickinson_and_co_z_0484_2026_2025,
  title = {Becton Dickinson & Co. — Class II recall: BD Kiestra" Isolate Suspension Cuvette Array;  Catalog No.: 246100;},
  author = {{Argus HQ Research}},
  year = {2025},
  publisher = {Digital Empire Holdings LLC},
  url = {https://argushq.ai/events/fda-recall-becton-dickinson-and-co-z-0484-2026},
  note = {Accessed: July 23, 2026}
}

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