Recall -- Firm Press Release
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MyNicKnaxs, LLC. Issues a Voluntary Nationwide and International Recall of All Weight Loss Formulas of Reduce Weight Fruta Planta
FOR IMMEDIATE RELEASE - February 4, 2014 - MyNicKnaxs, LLC., located in Florida is announcing a recall of Reduce Weight Fruta Planta because the products contain an undeclared active pharmaceutical ingredient: Phenolphthalein. The FDA lab analysis of the product found Reduce Weight Fruta Planta to contain 10.2 mg of Phenolphthalein. No illnesses or injuries have been reported to MyKnicKnaxs, LLC., in connection with these products.
Phenolphthalein was once an ingredient used in over-the-counter laxatives, but because of concerns of carcinogenicity is not currently approved for marketing in the United States. This undeclared ingredient makes Reduce Weight Fruta Planta an unapproved new drug for which safety and efficacy have not been established. Consumption of this product could include potentially serious gastrointestinal disturbances, irregular heartbeat, and cancer with long-term use.
All lots of the Reduce Weight Fruta Planta products are being recalled.
MyKnicKnaxs, LLC. has taken this voluntary action because it is committed to providing accurate information to all customers and is concerned for the health and safety of all users of Reduce Weight Fruta Planta. MyKnicKnaxs, LLC, is working with the FDA in the recall process. We sincerely regret any inconvenience the recall may cause customers.
Customers are advised to immediately discontinue use and Consumers with questions should contact mynicknaxs at 386-337-8142 or via e-mail at firstname.lastname@example.org Monday - Friday, 2pm - 7:00 pm, EDT.
Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.
- Online: www.fda.gov/medwatch/report.htm
- Regular Mail: use postage-paid, pre-addressed Form FDA 3500 available at: www.fda.gov/MedWatch/getforms.htm. Mail to address on the pre-addressed form.
- Fax: 1-800-FDA-0178
Photo: Product Labels
Recalled Product Photos Are Also Available on FDA's Flickr Photostream.