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Nationwide Reversitol Recall: Defective Dietary Supplement Lawyer & Lawsuit

iForce Nutrition recalling Reversitol, a product marketed as a dietary supplement containing ATD, because it does not meet FDA’s standard for dietary supplement classification.
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iForce Nutrition Issues a Nationwide Recall of Reversitol - a Product Marketed as a Dietary Supplement Containing ATD

Free Dietary Supplement Recall Case Evaluation: If you or a loved one has been injured by Reversitol, you should contact our law firm immediately. You may be entitled to compensation by filing a lawsuit and we can help.

What’s the problem?

September 20, 2010 - Tribravus Enterprises - LLC d/b/a/ iForce Nutrition - announced last week that it is conducting a nationwide recall of all Lot Codes of the company's dietary supplement product sold under the name Reversitol, which was marketed “for promoting hormonal regulation…,” and contains 6-Etioallochol-1,4-Diene-3,17-Dione, also known as ATD, an aromatase inhibitor. iForce Nutrition is conducting this recall after being informed by representatives of the Food and Drug Administration (FDA) that it is FDA’s opinion that 6-Etioallochol-1,4-Diene-3,17-Dione does not meet the definition of a dietary ingredient and therefore the product is in violation of provisions of the Food, Drug and Cosmetic Act.

Reversitol had been sold nationwide, both in retail stores and direct to consumers, but was discontinued by iForce Nutrition on December 10, 2009. The product was sold in red bottles with a white cap, containing sixty (60) capsules and was Manufactured for Distribution by Tribravus Enterprises, LLC. Although this product was discontinued nearly a year ago, it has come to the attention of iForce Nutrition that some online retailers may still have remaining inventory that they are offering for sale.

Aromatase Inhibitor Information

FDA has requested that iForce Nutrition inform consumers that adverse events associated with the use of aromatase inhibitors could include the following: decreased rate of bone maturation and growth, decreased sperm production, infertility, aggressive behavior, adrenal insufficiency, kidney failure, and liver dysfunction. Consumers with liver, kidney, adrenal, or prostate abnormalities are at higher risk for developing adverse events.

Do I have a Dietary Supplement Recall Lawsuit?

The Defective Drug & Product Liability Litigation Group at our law firm is an experienced team of trial lawyers that focus on the representation of plaintiffs in defective dietary supplement recall lawsuits. We are handling individual litigation nationwide and currently accepting new cases in all 50 states.

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