Friday, May 1, 2009

Hydroxycut Recalled

Hydroxycut is recalled after reports of liver failure, raising the question as to whether or not the FDA is adequate enough to regulate the supplement industry and protect public health.

At issue is the difference in the way the agency oversees drugs — defined as products that prevent or cure disease — and dietary supplements, which can offer general health benefits but cannot claim to treat specific diseases or symptoms.

Unlike drugs, whose manufacturers must provide safety and effectiveness data before receiving federal approval to sell the products, dietary supplements do not need prior F.D.A. sanction to go on sale. Manufacturers of dietary supplements are themselves responsible for ensuring and documenting the safety and efficacy claims of their products.

According to the law governing dietary supplements, the F.D.A. is empowered to act only in cases when it identifies a harmful or adulterated product that is already on sale. READ FULL ARTICLE

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