Hydroxycut Legal Resource Center


On May 1st 2009, the FDA announced a recall of 14 different Hydroxycut products in the wake of at least 23 reports of liver problems, including the death of a 19 year old. At least one patient required a liver transplant. Hydroxycut products are sold under both the “Iovate” and “Muscletech” brands. Hydroxycut is sold as a “dietary supplement” and as such, is not subject to the same level of scrutiny and testing by the FDA as prescription medicines, and does not require FDA approval to be sold. It is estimated that 9 million packages of Hydroxycut products were sold in 2008 through pharmacies, grocery stores, and supplement boutique stores.

Recalled Products

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Reported Symptoms

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Many athletes, bodybuilders, and those looking for an easier way to shed a few pounds have used Hydroxycut dietary supplements manufactured and distributed by Iovate Health Sciences and Muscletech, Inc. These supplements are marketed as “research supported” products that control hunger, increase metabolism, and boost energy, among other claims. Hydroxycut’s marketing literature proclaims, “The key ingredients in Hydroxycut® have been scientifically researched and combined to work optimally as indicated on the label.” Unfortunately, many consumers have reported suffering from serious illnesses while taking Hydroxycut supplements at their recommended dosages, including liver problems, seizures, cardiovascular disorders and rhabdomylolysis, a form of muscle damage that can cause kidney failure, and several other Hydroxycut symptoms. Shockingly, a 19 year old boy is reported to have died because of liver failure related to Hydroxycut usage. Symptoms of liver damage may include jaundice, brown urine, nausea, vomiting, excessive fatigue, weakness, stomach pain, itching and loss of appetite. Despite Iovate and Muscletech’s claims of its safety, Hydroxycut products have been implicated in an increasing number of injuries.

If you have been injured, learn more about your Hydroxycut legal options.

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