Severity
Moderate
FDA Food recall · Reported September 9, 2020
Recall required by Order of Permanent Injunction. The products are misbranded and deemed unapproved drugs based on labeling claims.
Sundial Herbal Products recalled Jamaican Bissy Powder; "***Bissy regulates the heart, removes and prevents water from set… - a moderate-severity action.
Jamaican Bissy Powder; "***Bissy regulates the heart, removes and prevents water from set… was recalled by Sundial Herbal Products in September 9, 2020. Reason: Recall required by Order of Permanent Injunction. The products are misbranded and deemed unapproved drugs bas…. Check the official notice for the remedy. Verify recall #F-1446-2020 with the FDA Food before acting.
The recall
Sundial Herbal Products issued this moderate-severity FDA Food recall-Recall required by Order of Permanent Injunction. The products are misbranded and deemed unapproved drugs bas….
Sourced from official FDA Food enforcement records. Verify recall #F-1446-2020 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
This FDA Food action (record #F-1446-2020) was formally reported on September 9, 2020, with the manufacturer initiating the action on June 30, 2020. It is classified under Moderate severity (Class II), with a current status of Terminated. Sundial Herbal Products is listed as the recalling firm, operating out of Bronx, NY. Federal records list the affected scope as Unknown.
The documented reason for this recall is: Recall required by Order of Permanent Injunction. The products are misbranded and deemed unapproved drugs based on labeling claims. Distribution data in the federal record shows the product reached: NY. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 1 from FDA Food - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Where this recall sits in its category - 14,287 drugs & medications recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Severity
Moderate
Affected scope
Unknown
Related Recalls
6
1 from same agency
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***"
Recall required by Order of Permanent Injunction. The products are misbranded and deemed unapproved drugs based on labeling claims.
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | F-1446-2020 |
| Date reported | September 9, 2020 |
| Date initiated | June 30, 2020 |
| Recalling firm | Sundial Herbal Products |
| Firm location | Bronx, NY |
| Affected scope | Unknown |
| Distribution | NY |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
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Lupin Pharmaceuticals Inc. · 2026-05-27
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Food, reported September 9, 2020. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.