Severity
Critical
CriticalClass ITerminated
FDA Food recall · Reported September 30, 2015
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 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
Firm's dietary supplements were being promoted for conditions that caused the products to be drugs under the FD&C Act.
Majopa Industries Corporation recalled Label reads in part as: "GRAVIOLA EXTRACT***1 FL Oz (30 ml)*** ORIGINAL FORMULA***Manufac… - a critical-severity action.
Label reads in part as: "GRAVIOLA EXTRACT***1 FL Oz (30 ml)*** ORIGINAL FORMULA***Manufac… was recalled by Majopa Industries Corporation in September 30, 2015. Reason: Firm's dietary supplements were being promoted for conditions that caused the products to be drugs under the …. Check the official notice for the remedy. Verify recall #F-3245-2015 with the FDA Food before acting.
The recall
Majopa Industries Corporation issued this critical-severity FDA Food recall-Firm's dietary supplements were being promoted for conditions that caused the products to be drugs under the ….
- Critical
- severity level
- Class I
- classification
- September 30, 2015
- reported
Sourced from official FDA Food enforcement records. Verify recall #F-3245-2015 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Food action (record #F-3245-2015) was formally reported on September 30, 2015, with the manufacturer initiating the action on July 31, 2015. It is classified under Critical severity (Class I), with a current status of Terminated. Majopa Industries Corporation is listed as the recalling firm, operating out of Guayama, PR. Federal records list the affected scope as 500 bottles.
The documented reason for this recall is: Firm's dietary supplements were being promoted for conditions that caused the products to be drugs under the FD&C Act. Distribution data in the federal record shows the product reached: Puerto Rico only. 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, 2 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.
Food recalls over time
Where this recall sits in its category - 25,126 food 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 high severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
500 bottles
Related Recalls
6
2 from same agency
Product description
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 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 for recall
Firm's dietary supplements were being promoted for conditions that caused the products to be drugs under the FD&C Act.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Critical (Class I) |
| Status | Terminated |
| Recall number | F-3245-2015 |
| Date reported | September 30, 2015 |
| Date initiated | July 31, 2015 |
| Recalling firm | Majopa Industries Corporation |
| Firm location | Guayama, PR |
| Affected scope | 500 bottles |
| Distribution | Puerto Rico only |
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.
- Check the recall number (F-3245-2015) and product description against the item you own. Search the archive
- Confirm the current status with FDA Food before acting, recall details can be updated.
- This is a Class I (high-risk) recall, stop using the product immediately and follow the disposal or return instructions. What to do next
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.
Frequently Asked Questions
What product was recalled? ▼
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 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".. Recalled by Majopa Industries Corporation. Units affected: 500 bottles.
Why was this product recalled? ▼
Firm's dietary supplements were being promoted for conditions that caused the products to be drugs under the FD&C Act.
Which agency issued this recall? ▼
This recall was issued by the FDA Food on September 30, 2015. Severity: Critical. Recall number: F-3245-2015.
Where was the recalled product distributed? ▼
Distribution: Puerto Rico only.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (F-3245-2015) against your product. Visit the official FDA Food website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
What are the health risks of consuming a recalled food product? ▼
Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.
Nearby Recalls in This Category
Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
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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 30, 2015. 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.