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fda_recall · device_recall · critical

Becton Dickinson & Company — Class I recall: BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in.; lidocaine HCL (1%), 5 mL,…

Event date
2026-06-10 00:00:00Z
Observed
2026-07-09 22:52:22Z
Source ID
Z-2256-2026
Payload hash
55c6d9d4d9f7f37f06384fc7

Summary

This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identified during an FDA manufacturing facility inspection, citing specific quality deficiencies related to acceptance testing. Status: Ongoing.

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 critical severity by Argus HQ. FDA published the underlying record on 2026-06-10; Argus observed and indexed it on 2026-07-09.
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). Becton Dickinson & Company — Class I recall: BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in.; lidocaine HCL (1%), 5 mL,…. Digital Empire Holdings LLC. Retrieved from https://argushq.ai/events/fda-recall-becton-dickinson-and-company-z-2256-2026
MLA
"Becton Dickinson & Company — Class I recall: BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in.; lidocaine HCL (1%), 5 mL,…." Argus HQ Research, Digital Empire Holdings LLC, 2026, argushq.ai/events/fda-recall-becton-dickinson-and-company-z-2256-2026.
Chicago
Argus HQ Research. "Becton Dickinson & Company — Class I recall: BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in.; lidocaine HCL (1%), 5 mL,…." Digital Empire Holdings LLC. Accessed August 27, 2026. https://argushq.ai/events/fda-recall-becton-dickinson-and-company-z-2256-2026.
BibTeX
@misc{argushq_argushq_ai_events_fda_recall_becton_dickinson_and_company_z_2256_2026_2026,
  title = {Becton Dickinson & Company — Class I recall: BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in.; lidocaine HCL (1%), 5 mL,…},
  author = {{Argus HQ Research}},
  year = {2026},
  publisher = {Digital Empire Holdings LLC},
  url = {https://argushq.ai/events/fda-recall-becton-dickinson-and-company-z-2256-2026},
  note = {Accessed: August 27, 2026}
}

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

Becton Dickinson & Company — Class I recall: BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in.; lidocaine HCL (1%), 5 mL,… · Argus HQ