How many FDA warning letters has Becton Dickinson & Company received?

Argus HQ has not recorded an FDA warning letter for Becton Dickinson & Company in our current dataset.

What FDA recalls has Becton Dickinson & Company issued?

Argus HQ has recorded 13 FDA recalls tied to Becton Dickinson & Company.

Is Becton Dickinson & Company FDA compliant?

Argus HQ is not a compliance rating service. As of this page's last update, our dataset shows 0 warning letters, 13 recalls, and 0 approval records for Becton Dickinson & Company. Review the linked FDA source records directly before drawing a compliance conclusion.

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company

Becton Dickinson & Company

Name: FDA Enforcement Actions Against Becton Dickinson & Company
Creator: Argus HQ
License: https://argushq.ai/methodology

Jurisdiction: US

FDA Warning Letter timeline

V1 scope: FDA Warning Letters only. Additional public-record sources (SEC, CPSC, federal contracts) are on the V2 roadmap and are not surfaced here today.

fda_recall · device_recall2026-06-10
Becton Dickinson & Company — Class I recall: BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in.; lidocaine HCL (1%), 5 mL,…
fda_recall · device_recall2026-06-10
Becton Dickinson & Company — Class I recall: BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in., BD¿Quincke Needle 22 G x…
fda_recall · device_recall2026-06-10
Becton Dickinson & Company — Class I recall: BD¿Spinal Tray with BD¿Quincke Needle 22 G x 3.5 in.; lidocaine HCL (1%), 5 mL,…
fda_recall · device_recall2026-06-10
Becton Dickinson & Company — Class I recall: BD¿Spinal Tray with BD¿Whitacre Needle 24 G x 3.5 in.; lidocaine HCL (1%), 5 mL,…
fda_recall · device_recall2026-06-10
Becton Dickinson & Company — Class I recall: BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in.; lidocaine HCL (1%), 2 mL,…
fda_recall · device_recall2026-06-10
Becton Dickinson & Company — Class I recall: BD¿Spinal Tray with BD¿Quincke Needle 26 G x 3.5 in.; lidocaine HCL (1%), 5 mL,…
fda_recall · device_recall2026-06-10
Becton Dickinson & Company — Class I recall: BD¿Spinal Tray with BD¿Whitacre Needle 22 G x 3.5 in.; lidocaine HCL (1%), 5 mL,…
fda_recall · device_recall2026-06-10
Becton Dickinson & Company — Class I recall: BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in.; lidocaine HCL (1%), 5 mL,…
fda_recall · device_recall2026-06-10
Becton Dickinson & Company — Class I recall: BD¿Spinal Tray with BD¿Quincke Needle 25 G x 3.5 in.; lidocaine HCL (1%), 5 mL,…
fda_recall · device_recall2026-06-10
Becton Dickinson & Company — Class I recall: BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in.; lidocaine HCL (1%), 5 mL,…
fda_recall · device_recall2026-05-27
Becton, Dickinson and Company — Class II recall: Swan-Ganz Jr Catheter, Models: SGPT54, SGPT64P, SGPT755P
fda_recall · device_recall2026-05-27
Becton, Dickinson and Company — Class II recall: Swan-Ganz Pacing Catheter, Models: D200F7;
fda_recall · device_recall2026-05-27
Becton, Dickinson and Company — Class II recall: Swan-Ganz Catheter, Models: 131F7/131F7P, 131F7J, 141F7, 151F7, 834F75, 096F6/09…

Frequently asked questions

How many FDA warning letters has Becton Dickinson & Company received?: Argus HQ has not recorded an FDA warning letter for Becton Dickinson & Company in our current dataset.
What FDA recalls has Becton Dickinson & Company issued?: Argus HQ has recorded 13 FDA recalls tied to Becton Dickinson & Company.
Is Becton Dickinson & Company FDA compliant?: Argus HQ is not a compliance rating service. As of this page's last update, our dataset shows 0 warning letters, 13 recalls, and 0 approval records for Becton Dickinson & Company. Review the linked FDA source records directly before drawing a compliance conclusion.

Informational only. FDA Warning Letters are public records (17 USC §105). Summaries are AI-assisted and may contain errors; always verify against the original FDA letter before acting. Not legal, financial, or regulatory advice.