FDA recall record
Label reads in part as: "GRAVIOLA EXTRACT***1 FL Oz (30 ml)*** ORIGINAL FORMULA***Manufactured by: Majopa Industries Corp.*** PRODUCT OF PUERTO RICO,USA". Drug claims in the...
FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.
FDA listed a termination date of March 29, 2017. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
*** PRODUCT OF PUERTO RICO,USA". Drug claims in the product label are as follows: "Researchers have found that Extracts from Graviola leaves can produce acetogenins which are extremely effective in the treatment of cancer cells. Graviola extract can works like an antibiotic against cancer cells by stopping growth of the enzymes needed for cell growth. It can be:cellular protector, anti tumorous, antiviral.
Also can be used as: Digestive stimulant, Strengthens immune system, antifungal, tranquilizer".
Reason
Firm's dietary supplements were being promoted for conditions that caused the products to be drugs under the FD&C Act.
Products involved
Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.
*** PRODUCT OF PUERTO RICO,USA". Drug claims in the product label are as follows: "Researchers have found that Extracts from Graviola leaves can produce acetogenins which are extremely effective in the treatment of cancer cells. Graviola extract can works like an antibiotic against cancer cells by stopping growth of the enzymes needed for cell growth. It can be:cellular protector, anti tumorous, antiviral.
Also can be used as: Digestive stimulant, Strengthens immune system, antifungal, tranquilizer".
Code information listed by FDA
02/2020
Distribution and firm information
Recalling firm listed by FDA: Majopa Industries Corporation
Firm location listed by FDA: Guayama, PR, United States
Distribution reported by FDA: Puerto Rico only
Product quantity listed by FDA: 500 bottles
Source
Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.
Official FDA openFDA food enforcement record
Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.