Hydroxycut Recall
May 1st, 2009The U.S. Food and Drug Administration (FDA) is warning consumers to immediately stop using Hydroxycut products by Iovate Health Sciences Inc., of Oakville, Ontario and distributed by Iovate Health Sciences USA Inc. of Blasdell, N.Y
Hydroxycut, one of the most popular diet pills on the market is being recalled due to reports of liver damage and other health problems. Hydroxycut accounts for about 90 percent of the market for weight loss supplements, with about 1 million bottles a year being sold.
The FDA announced today that the manufacturer of Hydroxycut just launched a nationwide recall of the dietary supplement. Hydroxycut is advertised as made from natural ingredients, but dietary supplements are not tightly regulated by the government like medications are, so manufacturers don’t need FDA approval before marketing their products.
FDA Warns Consumers to Stop Using Hydroxycut Products
“The FDA has received 23 reports of serious health problems ranging from jaundice and elevated liver enzymes, an indicator of potential liver injury, to liver damage requiring liver transplant. One death due to liver failure has been reported to the FDA. Other health problems reported include seizures; cardiovascular disorders; and rhabdomyolysis, a type of muscle damage that can lead to other serious health problems such as kidney failure.”
Hydroxycut Cleanse and Hoodia products are not affected by the recall. Consumers who have any of the products involved in the recall are advised to stop using them and to return them to the place of purchase.

