Product Wiki · Recalls · U.S. FDA — Food Enforcement

Recall F-3245-2015 — 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

U.S. FDA — Food Enforcement · United States · 2015-07-31 · Class I

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Agency: U.S. FDA — Food Enforcement
Recall identifier: F-3245-2015
Date of alert: 2015-07-31
Country / jurisdiction: United States
Risk level: Class I
Risk type: recall
Brand: Majopa Industries Corporation
Product category: food
Product type: Food

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

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

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