Home / Import refusals / 799-2232978-6/60001/1

FDA Import Refusal 799-2232978-6/60001/1 — Becton Dickinson & Company

Becton Dickinson & Company — FEI 2243072

The FDA refused shipment 799-2232978-6/60001/1 from Becton Dickinson & Company (United States) on October 9, 2025. The refused product falls under Devices — NEEDLE, HYPODERMIC, SINGLE LUMEN. Cited charges: 118,3280,508 This firm has 5 or more other import refusals on record.

Refusal Details

Date
October 9, 2025
Country
United States
Product Category
Devices
Product Code
80FMI NEEDLE, HYPODERMIC, SINGLE LUMEN
Charges
118,3280,508

Recent inspections

  • 1123595 (VAI Tue Mar 17 2020 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 809888 (VAI Tue Nov 20 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 635424 (NAI Thu Dec 03 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

Compliance actions

Other import refusals

  • 1FX-6704563-2/20002/1 (Mon Jun 01 2026 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 98F-0109418-2/11/2 (Thu May 29 2025 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • SCS-9072913-2/11/1 (Tue May 27 2025 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • SCS-9637208-5/11/1B (Fri May 02 2025 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • SCS-9637208-5/11/1A (Fri May 02 2025 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)

FDA data resources