Majopa Industries recalls graviola extract supplements labeled with drug claims like cancer treatment. Products may be illegal under FDA rules. Consumers should check labels for these claims.
Firm's dietary supplements were being promoted for conditions that caused the products to be drugs under the FD&C Act.
Majopa Industries is recalling graviola extract supplements that were labeled with drug claims such as cancer treatment. These claims are illegal under the FD&C Act because they promote products as drugs instead of dietary supplements.
The product was labeled with drug claims like treating cancer, acting as an antibiotic against cancer cells, and other medical benefits. These claims are illegal under the FD&C Act because dietary supplements cannot be marketed for drug effects.
People who bought or use Majopa's graviola extract supplements labeled with drug claims. Those who have purchased products with these specific claims are most at risk.
Check labels for 'GRAVIOLA EXTRACT', '1 FL Oz (30 ml)', 'ORIGINAL FORMULA', and 'Manufactured by: Majopa Industries Corp.' The products were sold in Puerto Rico, USA starting in February 2020.
Look for drug claims such as cancer treatment, antibiotic effects, or other medical benefits on the label.
The product was labeled with drug claims like treating cancer, which is illegal under the FD&C Act because dietary supplements cannot be marketed for drug effects.
The recall record does not specify a remedy, so check the label for drug claims and contact the manufacturer if unsure.
The recall is for illegal drug claims, not safety risks. The product itself is not considered dangerous, but the labeling is against FDA rules.
We’ve drafted a message you can send Majopa to request your refund or repair — edit it as you like.
Subject: Recall F-3245-2015 — Majopa Majopa Hello, I own a Majopa that is covered by recall F-3245-2015 from Majopa. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
