First Name:
Last Name:
Have any of the following complications occurred:
Liver Failure

Heart Attack
Kidney Disease
Liver Transplant
Other Serious Injury
Please describe any complications:
Please select all products taken:
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
Other (please explain below)
Where was the Hydroxycut product purchased?
The Vitamin Store
Other (list below)

Other comments/questions:

The FDA Recalls Hydroxycut

The FDA Hydroxycut Recall AddThis Social Bookmark Button

When there's a substantial risk involved with taking a medication or supplement, the U.S. Food and Drug Administration (FDA) issues a recall to warn consumers to stop taking it.

This is exactly what happened on May 1, 2009, when the FDA learned that popular weight loss drug Hydroxycut could be linked to major medical problems. Hydroxycut manufacturer Iovate has agreed to a voluntary recall of 14 different Hydroxycut products, and the FDA is urging consumers to discontinue use of all other Hydroxycut supplements as well.

The May 1, 2009 recall of Hydroxycut came after the FDA received over 20 reports of medical complications directly relating to the supplement. The most serious and common Hydroxycut problems are associated with liver failure, and one death has already been reported after a patient took Hydroxycut. This liver damage, which may cause the patient to need a liver transplant, has affected patients who were taken the recommended dosage. Other serious medical conditions that have been reported and contributed to the FDA's decision to recall Hydroxycut include seizures, muscle damage, heart disease, and kidney failure.

Do You Have A Hydroxycut Case? » Hydroxycut drug bottle

The FDA recommends that everyone taking Hydroxycut stops using the product, as even a lower dosage could lead to medical problems. The symptoms relating to serious conditions sometimes appear as soon as the patient begins taking Hydroxycut; other times, it is several months later or they even occur after the consumer stops taking the supplement.

Based on the information the FDA has received, it is impossible to tell which ingredient in the supplement or blend of ingredients causes the problems. The first liver-related problems were reported to the FDA many years ago, but at the time, it was thought that ephedra was the cause. Ephedra, however, was removed from Hydroxycut in 2004, and problems have since been reported. Because Hydroxycut is a supplement and not a drug, though, reporting on problems is not as highly regulated, and laws governing the product are different.

If you've experienced a problem due to taking Hydroxycut, you should see a doctor right away and also file a complaint with the FDA. It is important to also talk to a Hydroxycut lawyer to learn about your rights.

Contact Our Hydroxycut Recall Lawyers Today »
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