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FDA Import Refusal 1FX-3493444-8/10002/1 — Roche Diagnostics GmbH

Roche Diagnostics GmbH — FEI 3002806559

The FDA refused shipment 1FX-3493444-8/10002/1 from Roche Diagnostics GmbH (Germany) on Sep 18, 2026. The refused product falls under Devices — MULTIPLE USE BLOOD LANCET FOR SINGLE PATIENT USE ONLY. Cited charge: 3280 This firm has 5 or more other import refusals on record.

Refusal Details

Date
Sep 18, 2026
Country
Germany
Product Category
Devices
Product Code
79QRL MULTIPLE USE BLOOD LANCET FOR SINGLE PATIENT USE ONLY
Charges
3280

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Other import refusals

FDA data resources

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