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

Recent inspections

Other import refusals

FDA data resources

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.