FDA Import Refusal 1FX-4892980-6/10002/1 — Roche Diabetes Care GmbH

Roche Diabetes Care GmbH — FEI 3011806823

The FDA refused shipment 1FX-4892980-6/10002/1 from Roche Diabetes Care GmbH (Germany) on Jul 31, 2026. The refused product falls under Devices — SINGLE USE ONLY BLOOD LANCET WITHOUT AN INTEGRAL SHARPS INJURY PREVENTION FEATURE. Cited charges: 118,3280,341 This firm has 5 or more other import refusals on record.

Refusal Details

Date
Jul 31, 2026
Country
Germany
Product Category
Devices
Product Code
79QRK SINGLE USE ONLY BLOOD LANCET WITHOUT AN INTEGRAL SHARPS INJURY PREVENTION FEATURE
Charges
118,3280,341

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