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Consumers are advised to discontinue use of Hydroxycut products and consult a physician or health care professional if they are experiencing any symptoms of liver injury, which can include jaundice and brown urine, nausea, vomiting as well as unusual tiredness, unexplained itching and loss of appetite.

"Although liver damage appears to be rare, FDA feels consumers should not be exposed to unnecessary risk," said Dr. Linda Katz, interim chief medical officer at the Center for Food Safety and Applied Nutrition (CFSAN), part of the U.S. Food and Drug Administration (FDA)

The agency has received 23 reports of adverse liver effects including jaundice and liver damage severe enough to require organ transplant. Other individuals have experienced seizures, cardiovascular and other health problems. The medical literature also contains reports of liver issues in six patients taking Hydroxycut products.

The products being recalled are:

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

If you have been a victim of a Hydroxycut-related injury, speak to the experienced pharmaceutical litigation attorneys at Pollack & Flanders.