21 Day Weight Loss Kick Start Program! The FDA issued an alert in May 2009 regarding consumer technique weight loss product known as Hydroxycut. Not all Hydroxycut products were included in the recall, but the ones that were are suspected of causing serious liver damage in a few people.
The Hydroxycut recall issued by the FDA in May 2009 included a lot of the Hydroxycut line. Only Hydroxycut Cleanse and Hoodia products just weren't included. The recall came after certain things occurred. First, a law was enacted that required manufacturers of supplements to disclose serious illnesses connected to their products. The second thing that occurred was that the FDA received reports of 23 people experiencing liver damage due to use of Hydroxycut products. Consumers using one of the other 14 Hydroxycut products have been advised to halt using them immediately.
FDA dietary supplement director Vasilios Frankos stated in a Wall Street Journal article for the matter that 'it had been unclear' as to the specific Hydroxycut ingredients that are resulting in the liver damage. Additionally of note, other weight loss and energy products may contain the as-of-yet unidentified ingredients. Consumers are actually urged to evaluate with their physicians for more information about their personal risk level and then any possible drug/supplement interactions.
The following is a list of symptoms that is included with liver damage:
People with one of these symptoms are urged to find medical consultation immediately.
An FDA website article dated May 31, 2009 states there is really a correlation between genes and some liver damage due to medication. Though specific ties towards the Hydroxycut recall and this latest information have yet to be made, this information does provide hope for consumers that answers following the Hydroxycut warnings and recall may be forthcoming.
FDA Warns Consumers to Stop Using Hydroxycut Products. May 1, 2009. U.S. Department of Health & Human Services ' FDA U.S. Food and Drug Administration. News & Events ' Press Release.
FDA Warning: Stop Using Hydroxycut Products ' Liver Damage. May 2, 2009. US Recall News.
FDA Warns Consumers to Stop Taking Hydroxycut Products. Jared A. Favole. May 1, 2009. Wall Street Journal (online).
FDA and International Consortium Report New Data on Drug-Induced Liver Injury. May 31, 2009. U.S. Department of Health & Human Services ' FDA U.S. Food and Drug Administration. News & Events ' Press Release.
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