Iovate Initiates Voluntary Recall Of Hydroxycut Products After FDA Warning »
May 5, 2009
After learning that the U.S. Food and Drug Administration’s warning about Hydroxycut related products, Iovate initiated a voluntary recall.
Health Canada Alerts Canadians About Hydroxycut Products »
May 5, 2009
Health Canada, the regulatory authority that oversees health products in Canada, is alerting Canadians about Hydroxycut products after the U.S. Food and Drug Administration (FDA) issued a public warning regarding certain Hydroxycut products.
Government Health Officials Warn Dieters & Body Builders - Don't Use Hydroxycut »
May 4, 2009
Government health officials warned dieters and body builders Friday to immediately stop using Hydroxycut, a widely sold supplement linked to cases of serious liver damage and at least one death.
14 Hydroxycut Products Recalled In Warning Issued By FDA »
May 1, 2009
The U.S. Food and Drug Administration is warning consumers nationwide to stop using Hydroxycut products and has issued a recall for 14 products under the name brand weight loss drug.
Iovate Health Sciences U.S.A., Inc. Recalls Additional Hydroxycut Products »
May 7, 2009
Iovate Health Sciences USA, Inc. of Blasdell, New York and Ontario, Canada announced today that it is adding the following Universal Product Codes (UPCs) to the United States Hydroxycut Products recall.
FDA Tells Consumers To Immediately Stop Using Hydroxycut Products »
May 1, 2009
Consumers should "immediately stop" using Hydroxycut weight-loss products amid concerns they may cause jaundice and liver failure, the U.S. Food and Drug Administration said Friday.
Seeger Weiss Provides Legal Information about Hydroxycut Recall »
May 4, 2009
Seeger Weiss LLP seeks to help victims to know their legal rights after the FDA announced a recall of 14 different Hydroxycut products following at least 23 reports of liver problems, including one death of a 19-year-old boy.
