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Hydroxycut FDA Recall

The U.S. Food and Drug Administration (FDA) has issued a formal warning to consumers to stop using certain Hydroxycut diet supplements manufactured by Iovate Health Sciences, Inc. Hydroxycut Recall Full Article. This is in response to numerous reported cases of adverse health effects caused by the recalled product, such as liver failure, seizures, heart complications, and muscle damage. There has been one reported death caused by liver failure and two reports of Hydroxycut users undergoing liver transplants.

If you are using any of the recalled Hydroxycut products, you should discontinue use and seek immediate medical attention. The recalled products are:

Hydroxycut Caffeine-Free Caplets Hydroxycut Caffeine-Free Drink Packets Hydroxycut Carb Control Hydroxycut Hardcore Drink Packet (Ignition Stix)
Hydroxycut Hardcore Liquid Capsules Hydroxycut Hardcore RTD Hydroxycut Liquid Shot Hydroxycut Max Aqua Shed Hydroxycut Max Caplets Hydroxycut Max Drink Packet Hydroxycut Natural Hydroxycut Rapid Release Regular Caplets Hydroxycut Regular Drink Packet Hydroxycut 24
If you have used the recalled Hydroxycut product and suspect that you have been injured as a result, click here for help in evaluating your situation.

Robert J. Fleming is dedicated to helping Georgia consumers.

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