UMARY ACID HYALURONIC recalled over undeclared diclofenac
- Recall date
- November 14, 2024
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- MXBBB recalls UMARY ACID HYALURONIC, 850 MG CAPLETS, 30-count bottle, UPC7502265120323
- Recall number
- D-0166-2025
- FDA classification
- Class II
- Brand / firm
- MXBBB
- Sold / distributed
- Product was sold via Amazon Marketplace.
Why it was recalled
cGMP Deviations: the firm initiated a recall after notification from the distributor that product may be tainted with undeclared diclofenac and omeprazole, however there is no analytical data confirming that product distributed by the firm is tainted.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
UMARY ACID HYALURONIC, 850 MG CAPLETS, 30-count bottle, UPC7502265120323
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