Jamaican Bissy Powder — Class II food recall F-1446-2020
Terminated recall by Sundial Herbal Products, reported 2020-09-09, distributed in NY. Recall required by Order of Permanent Injunction. The products are misbranded and deemed unapproved drugs base
| Recall number | F-1446-2020 |
|---|---|
| Product type | Food |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | FDA mandated |
| Recalling firm | Sundial Herbal Products, Bronx, NY, United States |
| Recall initiated | 2020-06-30 |
| Classified | 2020-09-15 |
| Reported by FDA | 2020-09-09 |
| Terminated | 2022-10-26 |
| Distributed | NY |
| Reason classes | labeling, unapproved product |
Product
Jamaican Bissy Powder; "***Bissy regulates the heart, removes and prevents water from settling around the heart, lessens the desire for drugs, cigarettes, alcohol by clearing the body and blood of poison viruses & toxins etc. Relieves fatigue gives stamina and endurance enabling one to do heavy work without getting tired. The tea also relieves depression, headaches, diarrhea, and dysentery. It's used as antibiotic and antidote***Always have Sundial Bissy and Sundial Ethiopian mitmita (Cayenne pepper) for all medical emergencies***"
Reason for recall
Recall required by Order of Permanent Injunction. The products are misbranded and deemed unapproved drugs based on labeling claims.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/F-1446-2020. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.