Mitmitta 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 Mitmitta (Cayenne Pepper); "Traditional Uses: Prevents heart attacks, and lowers high blood pressure, stops internal bl…
- Recall number
- F-1448-2020
- 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
Mitmitta (Cayenne Pepper); "Traditional Uses: Prevents heart attacks, and lowers high blood pressure, stops internal bleeding, Heals ulcers and pains there of: Improves circulation, thins blood and keeps it moving***"
Get recall alerts
Free email alert whenever Sundial Herbal Products has a new recall — straight from official government data. Unsubscribe anytime.
More recalls from: Sundial Herbal Products