FDA Import Refusal 1FX-3603340-5/10002/1 — Roche Diabetes Care GmbH

Roche Diabetes Care GmbH — FEI 3011806823

The FDA refused shipment 1FX-3603340-5/10002/1 from Roche Diabetes Care GmbH (Germany) on Aug 23, 2026. The refused product falls under Devices — SINGLE USE ONLY BLOOD LANCET WITHOUT AN INTEGRAL SHARPS INJURY PREVENTION FEATURE. Cited charges: 118,3280,341,508 This firm has 5 or more other import refusals on record.

Refusal Details

Date
Aug 23, 2026
Country
Germany
Product Category
Devices
Product Code
79QRK SINGLE USE ONLY BLOOD LANCET WITHOUT AN INTEGRAL SHARPS INJURY PREVENTION FEATURE
Charges
118,3280,341,508

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