Breaking News on Supplements & Nutrition - North AmericaEU edition

On your radar > GMPs, QA & QC

FDA files permanent injunction against supplement manufacturer

3 commentsBy Stephen Daniells, 25-Nov-2011

Related topics: GMPs, QA & QC, Industry

The US Food and Drug Administration has filed for a permanent injunction against a Pennsylvania dietary supplement manufacturer as the agency turns the GMP compliance screw.

“Today’s injunction reinforces our commitment to ensuring that these supplements meet the cGMP requirements the law establishes" - Dara Corrigan, FDA.

“Today’s injunction reinforces our commitment to ensuring that these supplements meet the cGMP requirements the law establishes" - Dara Corrigan, FDA.

The injunction – the first of its kind against a dietary supplement manufacturer of this size for failure to comply with cGMP (current Good Manufacturing Practice) – would stop the defendants ATF Fitness Products Inc. from making and distributing more than 400 products for being in violation of the Federal Food, Drug, and Cosmetic Act.

“Dietary supplements have a significant role in the public’s health,” said Dara Corrigan, associate commissioner for regulatory affairs.

“Today’s injunction reinforces our commitment to ensuring that these supplements meet the cGMP requirements the law establishes.”

The injunction was filed by the US Department of Justice on behalf of the FDA against ATF Fitness Products Inc. (ATF), Manufacturing ATF Dedicated Excellence, Inc. (MADE), and James G. Vercellotti of Oakmont, Pa., owner and operator of both companies.

MADE reportedly manufactures over 400 dietary supplements, which are purchased by ATF for distribution throughout the US.

ATF received two warning letters in 2004, one for the labeling and/or promoting of a dietary supplement that contained androstenedione as an ingredient , and the second for “dietary supplement products that are labeled to contain materials that are sources of ephedrine alkaloids” .

This was followed by a seizure by US Marshals in 2006 of ATF’s Lipodrene dietary supplement were said to contain ephedrine alkaloids .

On November 23, 2011, the government filed a complaint in the US District Court for the Western District of Pennsylvania, alleging that in addition to “adulterating” and “misbranding” their final products, the manufacturer and its owner failed to report serious adverse events associated with their products.

Indeed, in one case an individual who consumed one of the products reported experiencing a spike in blood pressure, hospitalization and a subsequent mild heart attack.

3 comments (Comments are now closed)

Government involvement

I think it is sad the government has to take on such an intrusive role to prevent everyone from misusing substances, or basically being stupid. We all know whats smart to do and what effects certain supplements might have on us. Why we need to have our hands held like babies and cant even buy andro or ephedrine PERIOD is just absurd...i am a female fitness Npc competitor and i wish i didnt have beaurocrats telling me what i should do with my body. If i take too much or DIE thats my damn fault for not educating myself first.

Report abuse

Posted by Lisa butz
27 November 2011 | 22h18

Make your mind up

For so long the medics have been telling us that Vitamins are a waste of money now the FDA are saying something different. The people of america need to get the FDA disbanded

Report abuse

Posted by JB
25 November 2011 | 22h56

This is a warranted sanction

I am not often a fan of the FDA's treatment of supplement makers; however in this case it appears reasonably clear that the action was justified. Bad actors should not be defended by the industry, and legal non-discriminatory enforcement, after due process is afforded the company involved, is good for all of us.

Report abuse

Posted by James Betz
25 November 2011 | 16h25

Supplier Webinars