FDAFDA · Food and drugs·Recall number F-1499-2020
"AXUM ETHOIPIAN HONEY BEVERAGE***SUNDIAL HERBS***"
Published September 9, 2020 · Recall initiated: June 30, 2020
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Recall required by Order of Permanent Injunction. The products are misbranded and deemed unapproved drugs based on labeling claims.
What to do
FDA Mandated · Letter
Recall details
- Manufacturer
- Sundial Herbal Products
- Distributor
- NY
- Lot
- Product manufactured, processed, packed, held, and/or distributed during the time period beginning 1/1/2014 through 5/27/2020.
- Risk classification
- Class II
- Area (FDA)
- food
- Country
- United States
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