Exact FDA event identifier

Event 71918

1 recalled-product record grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket: July 31, 2015
Product types: Food
Classifications: Class I
Statuses: Terminated
Recalling firm wording: Majopa Industries Corporation

Dossier provenance

Source snapshots represented here

openFDA Food Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Device root-cause evidence is not applicable to this event. No grouped product has the official product type device; this is not an unavailable-enrichment finding.

Complete imported group

Every recalled product in this event

1 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

food · product 1 of 1

Label reads in part as: "GRAVIOLA EXTRACT1 FL Oz (30 ml) ORIGINAL FORMULAManufactured 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".

F-3245-2015

Recall number: F-3245-2015
Initiated: July 31, 2015
Classification: Class I
Status: Terminated
Recalling firm: Majopa Industries Corporation
Quantity: 500 bottles

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

Firm's dietary supplements were being promoted for conditions that caused the products to be drugs under the FD&C Act.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Firm's dietary supplements were being promoted for conditions that caused the products to be drugs under the FD&C Act.

Code information

02/2020

Distribution pattern

Puerto Rico only