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Recall Number: F-1446-2020

Why was 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***" recalled?

Recall required by Order of Permanent Injunction. The products are misbranded and deemed unapproved drugs based on labeling claims.

Check out this page for guidance on what to do if you've consumed food from recall F-1446-2020 .

Sundial Herbal Products recall in Bronx, NY details
Here's recall specific data. Click on the company, city, or state for more recalls by Sundial Herbal Products or more recalls in Bronx or New York.

  • City: Bronx

  • State: New York

  • Country: United States

  • Classification: Class II

  • Classification Date: 2020-09-15

  • Reason: Recall required by Order of Permanent Injunction. The products are misbranded and deemed unapproved drugs based on labeling claims.

  • Product Description: 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***"

  • Report Date: 2020-09-09

  • Product Type: Food

  • Company: Sundial Herbal Products

  • Status: Terminated

  • Recall Number: F-1446-2020

  • Postal Code: 10466-5810

  • Recall Initiation Date: 2020-06-30

  • Recall End Date: 2022-10-26

  • Event ID: 85882

  • Distribution Pattern: NY

  • Voluntary Or Mandated: FDA Mandated

  • Initial Firm Notification: Letter

  • Extra Info: Product manufactured, processed, packed, held, and/or distributed during the time period beginning 1/1/2014 through 5/27/2020.

  • Product Quantity: Unknown

  • Address: 3609 Boston Rd

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