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  • Two Hydroxycut Class Actions Filed

    by Stacey E. Burke on May 29, 2009

    Hydroxycut was voluntarily recalled on May 1 after the Food and Drug Administration (FDA) identified numerous health risks posed by the drug. The Administration received 23 complaints of liver damage resulting from use of the product, ranging from jaundice to the need for a transplant.

    The drug poses other serious risks, including heart failure, seizures, and rhabdomyolysis, a muscle condition where muscle fibers break down to the point that they are released into the bloodstream. In some serious cases, this condition can lead to kidney failure.

    The Tennessee suit defines a class of anyone who purchased a Hydroxycut product. The lead plaintiffs spent varying amounts of money on Hydroxycut products before the recall was announced.  The plaintiffs in the Tennessee action experienced a number of symptoms as a result of taking the drug, including nausea, vomiting, abdominal pain, headaches, and extreme fatigue.

    The FDA said that, while liver damage is rare, those affected did not exceed the recommended dosage of the drug. The Administration has yet to determine why the drug causes such damage.

    The list of products being recalled by Iovate currently includes:

    • Hydroxycut Regular Rapid Release Caplets
    • Hydroxycut Caffeine-Free Rapid Release Caplets
    • Hydroxycut Hardcore Liquid Caplets
    • Hydroxycut Max Liquid Caplets
    • Hydroxycut Regular Drink Packets
    • Hydroxycut Caffeine-Free Drink Packets
    • Hydroxycut Hardcore Drink Packets (Ignition Stix)
    • Hydroxycut Max Drink Packets
    • Hydroxycut Liquid Shots
    • Hydroxycut Hardcore RTDs (Ready-to-Drink)
    • Hydroxycut Max Aqua Shed
    • Hydroxycut 24
    • Hydroxycut Carb Control
    • Hydroxycut Natural

    The FDA has not yet determined which ingredients, dosages, or other health-related factors may be associated with risks related to these Hydroxycut products. The products contain a variety of ingredients and herbal extracts.

    If you or a loved one has been injured or died after taking Hydroxycut, you may be eligible to receive compensation from the makers of Hydroxycut or other responsible parties and/or entitled to wrongful death damages.  Please contact SMSH at (800) 282-2122.

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