September 16, 2013 — The U.S. Food and Drug Administration (FDA) and Ge Pharma, LLC have issued a recall for Creafuse Powder because it contains DMAA, an illegal stimulant drug also known as 1,3-dimethylamylamine.
Products in the Creafuse Powder recall include:
- Creafuse Powder Grape Lot# GE4568
- Creafuse Powder Fruit Punch Lot #GE4570
The products were sold nationwide via telephone and email. They are packaged in a white, 600-gram container with an expiration date of February 2015. Ge Pharma requests that customers should stop using the product, report adverse events to a doctor and the FDA, and contact the company for a refund.
According to the FDA:
“The FDA has warned that DMAA is potentially dangerous to health. Ingestion of DMAA can elevate blood pressure and lead to cardiovascular problems. A number of adverse effects associated with DMAA containing dietary supplements have been reported to the FDA.”
The FDA has been cracking down on DMAA supplements since mid-2012. The enforcement began with a series of warning letters to 10 manufacturers. Most of the manufacturers stopped selling DMAA or reformulated their products.
However, the largest manufacturer, USPLabs, argued that the stimulant was an all-natural extract of the geranium plant. The FDA disagreed. In July 2013, more than $8 million worth of Jack3D and OxyElite Pro were destroyed by USPLabs.
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