Home / Import refusals / 1FX-5546642-8/10001/1C

FDA Import Refusal 1FX-5546642-8/10001/1C — Terumo Europe

Terumo Europe — FEI 3001570557

The FDA refused shipment 1FX-5546642-8/10001/1C from Terumo Europe (Belgium) on June 4, 2026. The refused product falls under Devices — NEEDLE, HYPODERMIC, SINGLE LUMEN. Cited charges: 118,3280,341,508 This firm has 4 other import refusals on record.

Refusal Details

Date
June 4, 2026
Country
Belgium
Product Category
Devices
Product Code
80FMI NEEDLE, HYPODERMIC, SINGLE LUMEN
Charges
118,3280,341,508

Recent inspections

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Other import refusals

  • BMI-0081837-8/2001/1 (Wed Jun 26 2024 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 799-9083138-0/61/1 (Fri Jan 19 2024 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 112-7556875-1/1/1D (Tue Aug 07 2012 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 112-1577726-2/2/1 (Fri Aug 22 2008 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)

FDA data resources