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All Press Releases for May 15, 2009 Subscribe to this News Feed    
 

Aiken & Scoptur - FDA to Dieters: Stop Using Hydroxycut

Aiken & Scoptur reports on The Food and Drug Administration warned dieters and body builders to immediately stop using Hydroxycut after the FDA received reports of liver damage and other health problems. The FDA said the maker of the popular dietary supplement has issued a voluntary nationwide recall of 14 Hydroxycut products.

Milwaukee, WI (PRWEB) May 15, 2009 -- Aiken & Scoptur, S.C. Please visit our Web site at http://plaintiffslaw.com.

The Food and Drug Administration warned dieters and body builders to immediately stop using Hydroxycut after the FDA received reports of liver damage and other health problems. The FDA said the maker of the popular dietary supplement has issued a voluntary nationwide recall of 14 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 transplants." Other reported health problems include seizures, cardiovascular disorders and a type of muscle damage that can lead to kidney failure.

The FDA said one death due to liver failure has been reported. In a statement, the agency said it is "important to note that even people who had no pre-existing medical conditions have needed liver transplants after taking Hydroxycut."

Hydroxycut products are sold for weight loss, as fat burners, energy-enhancers, low-carbohydrate diet aids and for water loss under the Iovate and MuscleTech brand names.

Iovate Health Sciences, Canadian makers of the diet and body building pills, reportedly sold over nine million packages of the pills last year.

"The FDA urges consumers to discontinue use of Hydroxycut products in order to avoid any undue risk. Adverse events are rare, but exist. Consumers should consult a physician or other health care professional if they are experiencing symptoms possibly associated with these products," said Linda Katz, M.D., interim chief medical officer of the FDA's Center for Food Safety and Applied Nutrition.

Recalled Hydroxycut products

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 any of the listed products, the FDA urges you to return it to the place of purchase.

Consumers and medical professionals are encouraged to report serious adverse side effects associated with the use of the listed Hydroxycut products.

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CONTACT INFORMATION
Tim Aiken
Aiken & Scoptur, S.C.
414-225-0260 x53226
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