Judge Rules Against Hi-Tech, DMAA in FDA Litigation

The U.S. government has prevailed in a years-long lawsuit against Hi-Tech Pharmaceuticals, even though a judge determined FDA failed to meet its burden of proof that DMAA is not in the geranium plant.

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Judge Rules Against Hi-Tech, DMAA in FDA Litigation

Despite rejecting a number of FDA’s arguments in a lawsuit, a federal judge in Atlanta on Monday concluded on his own that DMAA (1, 3-dimethylamylamine) is not a dietary ingredient.

FDA has prevailed—at least for the time being—in a years-long fight to remove the controversial ingredient from the dietary supplement market.

The decision, however, is unlikely to resolve a debate between regulators and industry over the legality of substances that can be found in plants but are made synthetically for use in products like sports supplements.

Federal Judge Willis B. Hunt, Jr., acknowledged the economic benefits of chemical synthesis, and he didn’t rule out the possibility that botanicals could qualify as a dietary ingredient even if a substance like DMAA was synthetized in a lab.

But Hunt observed DMAA is only present, at best, in “miniscule amounts" and has never been extracted from geranium plants for a commercial purpose.

In using the term botanical in the Dietary Supplement Health and Education Act (DSHEA), Hunt concluded “Congress intended that there must be at least some history of the substance in question having been extracted in usable quantities from a plant or a plant-like organism…."

The judge also determined products containing DMAA don’t meet a safety standard for food, rendering them adulterated and subject to seizure.

FDA, the U.S. Department of Justice and Hi-Tech Pharmaceuticals Inc.—whose DMAA products are the subject of the case—did not immediately respond to requests for comment.

Appeal to Eleventh Circuit Likely

The summary judgment order marked a blow to Hi-Tech, a supplement manufacturer that has sold tens of millions of dollars in products containing DMAA, and its owner, Jared Wheat.

In a recent interview with INSIDER, Wheat vowed to file an appeal if his company lost in the district court in the Northern District of Georgia.

The U.S. Court of Appeals for the Eleventh Circuit is not far from Hi-Tech’s headquarters in Norcross, Georgia.

“My stance has always been: I fight," he said. “Sometimes that is a bad business decision, but it is just who Hi-Tech is and who I am as a person—I never play to lose."

For now, the decision only has “precedent in the Northern District of Georgia," said Marc Ullman, of counsel to the law firm Rivkin Radler LLP, “though it exposes what we've thought to be a real weakness in FDA's position on synthetic botanicals."

FDA Definition of Botanical: ‘Arbitrary’

In examining whether DMAA qualifies as a botanical dietary ingredient, the judge concluded FDA’s definition of a botanical was “arbitrary and not entitled to deference."

The government described a botanical as “a plant, alga, or fungus, or a physical part or secretion of a plant, alga, or fungus, such as bark, leaves or fruits." An FDA supplement official had essentially provided the same definition, as did a 2016 FDA guidance document referenced by the official.

Hunt, however, was not persuaded.

“The FDA publication merely purports to provide guidance to industry regarding the requirements of providing notice to the FDA relating to new dietary ingredients," the judge observed. “The publication does not appear to be a scientific paper and there is no indication of who wrote it. In short, the government has failed to provide an adequate basis for its interpretation of congressional intent in using the term 'botanical' in § 321(ff)" of DSHEA.

FDA Failed to Meet Burden of Proof

In his 14-page decision, Hunt determined FDA failed to meet its burden of proof that DMAA is not in geraniums. He pointed to a 2013 research paper, which examined studies that showed DMAA had been found naturally in some, but not all, extracted geranium oils and geranium plants.

“It is undisputed that at least three different studies found DMAA in geraniums, and the fact that other studies, which may well have used different methodologies, did not detect DMAA is not determinative," Hunt wrote.

The judge was “unswayed" by the government’s assertion there was no possible metabolic pathway for the plant to make DMAA. The testimony from the government’s expert in support of FDA’s position, he said, was “nowhere near as unequivocal."

Hunt also addressed FDA’s claim that the geraniums from one of the studies may have been tainted with fertilizer that contained DMAA. “The argument fails to address the fact that other studies did find DMAA," he pointed out.

Court Interprets Intent of DSHEA on Botanicals 

Hunt appeared to endorse the notion that a botanical can be synthetized in a lab and still qualify as a dietary ingredient under DSHEA. FDA has taken a contrary position in its 2016 new dietary ingredient (NDI) guidance, the same document Hunt referenced that defined a botanical.

Chemical synthesis, Hunt wrote, is frequently more economical than extracting a compound from a plant, and the judge indicated the inability to synthetize from a botanical without violating DSHEA could threaten a plant’s existence.

Still, the fact that only trace amounts of DMAA were detected in geraniums led the court to rule in favor of the government and against Hi-Tech.

“Nonetheless, it is inconceivable that in passing the DSHEA Congress intended for supplement manufacturers to take a chemical that heretofore had only been manufactured in a laboratory and to scour the globe in search of minuscule amounts of that chemical in obscure plants so that they could declare the substance a dietary ingredient under the statute," Hunt wrote.

“To hold otherwise," the judge continued, “would be to open the door to bogus claims that, for example, a given chemical had been detected in a fungus found only in a remote Tibetan river valley, and the FDA would be left to refute that claim—to prove a negative—which the instant case demonstrates is not easily done."

DMAA: Food Additive and Not GRAS

The judge concluded DMAA is not a botanical and therefore not a dietary ingredient. DMAA is a food additive that is presumed unsafe, the judge noted, unless it is generally recognized as safe (GRAS).

“This court’s conclusion after reading the various expert reports and other documents is that there is no consensus regarding the question of whether the consumption of DMAA is safe," Hunt wrote.

The judge cited the exhaustive research review in a DMAA product liability case in Texas, which found insufficient evidence that DMAA is safe. He further noted many scientists have expressed safety concerns about DMAA, including its potentially similar effects to amphetamines. While Hi-Tech provided evidence of no adverse effects, the judge said the sample sizes used in the studies submitted were too small to draw definitive conclusions.

“Hi-Tech has failed to present sufficient evidence to demonstrate that consensus, leading to the further conclusion that DMAA is not generally recognized as safe under the FDCA [Federal Food, Drug, and Cosmetic Act]," he wrote.

Hunt determined Hi-Tech’s DMAA-containing products are adulterated and subject to seizure. Finally, he rejected Hi-Tech’s claims that the government violated the FDCA, DSHEA, the Administrative Procedures Act or the U.S. Constitution’s Fifth Amendment.

Anthony Roberts, an independent journalist, first reported the court decision on Medium.

About the Author(s)

Steve Myers

Senior Editor

Steve Myers is a graduate of the English program at Arizona State University. He first entered the natural products industry and Virgo Publishing in 1997, right out of college, but escaped the searing Arizona heat by relocating to the East Coast. He left Informa Markets in 2022, after a formidable career focused on financial, regulatory and quality control issues, in addition to writing stories ranging research results to manufacturing. In his final years with the company, he spearheaded the editorial direction of Natural Products Insider.

Josh Long

Associate editorial director, Natural Products Insider, Informa Markets Health and Nutrition

Josh Long directs the online news, feature and op-ed coverage at Natural Products Insider, which targets the health and wellness industry. He has been reporting on developments in the dietary supplement industry for over a decade, with a focus on regulatory issues, including at the Food and Drug Administration.

He has moderated and/or presented at industry trade shows, including SupplySide East, SupplySide West, Natural Products Expo West, NBJ Summit and the annual Dietary Supplement Regulatory Summit.

Connect with Josh on LinkedIn and ping him with story ideas at [email protected]

Education and previous experience

Josh majored in journalism and graduated from Arizona State University the same year "Jake the Snake" Plummer led the Sun Devils to the Rose Bowl against the Ohio State Buckeyes. He also holds a J.D. from the University of Wyoming College of Law, was admitted in 2008 to practice law in the state of Colorado and spent a year clerking for a state district court judge.

Over more than a quarter century, he’s written on various topics for newspapers and business-to-business publications – from the Yavapai in Arizona and a controversial plan for a nuclear-waste incinerator in Idaho to nuanced issues, including FDA enforcement of the Dietary Supplement Health and Education Act of 1994 (DSHEA).

Since the late 1990s, his articles have been published in a variety of media, including but not limited to, the Cape Cod Times (in Massachusetts), Sedona Red Rock News (in Arizona), Denver Post (in Colorado), Casper Star-Tribune (in Wyoming), now-defunct Jackson Hole Guide (in Wyoming), Colorado Lawyer (published by the Colorado Bar Association) and Nutrition Business Journal.

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