SUNDIAL NIGERIAN MORINGA LEAF POWDER recalled over labeling errors
- Recall date
- June 30, 2020
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- Sundial Herbal Products recalls SUNDIAL NIGERIAN MORINGA LEAF POWDER; "***Anti-inflammatory, builds Red Blood cells***" 4oz and 8oz jars
- Recall number
- F-1442-2020
- FDA classification
- Class II
- Brand / firm
- Sundial Herbal Products
- Sold / distributed
- NY
Why it was recalled
Recall required by Order of Permanent Injunction. The products are misbranded and deemed unapproved drugs based on labeling claims.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
SUNDIAL NIGERIAN MORINGA LEAF POWDER; "***Anti-inflammatory, builds Red Blood cells***" 4oz and 8oz jars
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