Hydroxycut® Recall

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HYDROXYCUT® products RECALLED
due to risk of serious liver injury.

Hydroxycut® dietary supplement and weight loss products were recalled this year by the manufacturer and distributor because of an association with serious liver injuries, including death due to liver failure. The Food and Drug Administration issued a warning to consumers to immediately stop use of all Hydroxycut products, and posted a letter to all Health Care Professionals, warning of a potential risk of severe liver injury from the use of these products. Reported adverse events included hyperbilirubinemia, jaundice, liver damage, liver transplant and death. None of the 23 reported cases had any risk factors or diseases associated with liver disease or injury. In some instances, discontinuation of the Hydroxycut product resulted in recovery of liver function.

Hydroxycut® is distributed by Iovate Health Sciences, Inc. of Oakville, Ontario and Iovate Health Sciences USA, Inc. of Blasdell, New York. It is reported to be the number one selling over-the-counter dietary supplement for weight loss. The list of recalled products includes:

We are actively investigating nationwide Hydroxycut side effect claims.  If you or a loved one experienced serious liver injuries due to the use of Hydroxycut, please contact the national law firm of Nadrich & Cohen at 800-718-4658.  We are reviewing Hydroxycut injury claims from coast to coast.

If you or a loved one has suffered a serious liver injury due to Hydroxycut, contact an experienced Hydroxycut Injury Lawyer at Nadrich & Cohen, LLP

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