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December 1st, 2010

Unless otherwise noted, news announcements are presented in their entirety and authored by the issuing company.

Washington — The Senate on Tuesday passed a sweeping overhaul of the nation’s food-safety system, after recalls of tainted eggs, peanut butter and spinach that sickened thousands and led major food makers to join consumer advocates in demanding stronger government oversight.

The legislation, which passed by a vote of 73 to 25, would greatly strengthen the Food and Drug Administration, an agency that in recent decades focused more on policing medical products than ensuring the safety of foods. The bill is intended to get the government to crack down on unsafe foods before they harm people rather than after outbreaks occur.

Despite unusual bipartisan support on Capitol Hill and a strong push from the Obama administration, the bill could still die because there might not be enough time for the usual haggling between the Senate and House of Representatives, which passed its own version last year. Top House Democrats said that they would consider simply passing the Senate version to speed approval.

Both versions of the bill would grant the F.D.A. new powers to recall tainted foods, increase inspections, demand accountability from food companies and oversee farming. But neither version would consolidate overlapping functions at the Department of Agriculture and nearly a dozen other federal agencies that oversee various aspects of food safety, making coordination among the agencies a continuing challenge.

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Categories : Food
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Tainted Dietary Supplements and Foods

FDA

October 13, 2010
www.fda.gov

What are Tainted Supplements/Foods?
In recent years, FDA has identified hundreds of products marketed as dietary supplements or conventional foods with hidden drugs and chemicals. The products are typically promoted for sexual enhancement, weight loss, bodybuilding, and diabetes. FDA lab analyses have found products that have been laced with a wide variety of potentially dangerous ingredients that include:
• Approved prescription drug ingredients and their analogues
• Drugs banned by FDA for safety reasons
• Controlled substances such as anabolic steroids and stimulant diet drugs
• New active drug ingredients that are untested and unstudied

Health Risks
Tainted products place consumers at risk of injury and death, especially those consumers with underlying health conditions. These products can also interact in life threatening ways with other medications a consumer may be taking.

Know What’s in Your Products
FDA is becoming more active in pursuing criminal convictions for sellers of tainted supplements. For example, in 2010, VMG Global was convicted of a felony and fined for selling supplements laced withanabolic steroids; in recent months, FDA has brought misdemeanor charges against several persons for selling sexual enhancement supplements with hidden active pharmaceutical ingredients.

Requirements Under the Law
Anyone who sells or distributes these illegal products may be subject to:
• Criminal liability — misdemeanors and felonies
• Seizure of your products
• Injunction of the responsible party or company
• Disgorgement of profits and restitution

Retailers and distributors are responsible under the Federal Food Drug and Cosmetic Act (FFDCA) for ensuring that the products they sell are safe and properly labeled. A company cannot escape the law by relying on a manufacturer’s or supplier’s representations that the product is not tainted.

Download a PDF of this statement

Watch Out for These Red Flags

• Product Categories:
• Sexual Enhancement
• Weight Loss
• Bodybuilding
• Diabetes

• Labeling claims like:
• “Alternative to [approved drug product]”
• “Do not take if you have any medical condition, if you are taking any prescription medications,
• or if you are pregnant”
• “May cause positive result in performance enhancing drug test”

• Labels primarily in a foreign language
• Beware of mass solicitations (particularly emails) from suppliers and wholesalers offering products in the above categories.
• Directions and warnings that resemble FDA approved drug products

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