FDA Import Refusal AEK-0768116-5/10002/1 — Q-Med AB

Q-Med AB — FEI 3003347293

The FDA refused shipment AEK-0768116-5/10002/1 from Q-Med AB (Sweden) on Oct 1, 2026. The refused product falls under Devices — IMPLANT, DERMAL, COLLAGEN FOR AESTHETIC USE. Cited charges: 118,237,3280 This firm has 5 or more other import refusals on record.

Refusal Details

Date
Oct 1, 2026
Country
Sweden
Product Category
Devices
Product Code
79LMH IMPLANT, DERMAL, COLLAGEN FOR AESTHETIC USE
Charges
118,237,3280

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