Electronic-cigarette maker Juul has filed a lawsuit against the Food and Drug Administration (FDA) after the agency earlier this year ordered the company to remove its products from stores in the United States.
Washington, D.C.-based Juul was ordered back in June to remove its e-cigarettes off the shelves in the U.S. market after the FDA said the company’s application “lacked sufficient evidence” regarding the toxicology levels of the products.
“Less than a day after FDA’s decision, JLI served two Freedom of Information Act (‘FOIA’) requests for the scientific disciplinary reviews underlying FDA’s decision,” the lawsuit states.
“The agency invoked one of the most widely abused exemptions—the deliberative process privilege—to withhold the majority of those materials,” lawyers for the company wrote.
‘Public Deserves a Complete Picture’
“Withholding the disciplinary reviews that would answer these questions impedes JLI’s ability to seek appropriate relief from [the] FDA’s decision and is also completely at odds with the purpose of the FOIA and the transparency Congress expects from administrative agencies,” the complaint alleges.The company accused the FDA of violating the Freedom of Information Act, and asked that the court to “assume jurisdiction in this matter and maintain jurisdiction until the FDA complies with FOIA and every order of this court.”
They also asked that the court to prevent the FDA from continuing to withhold the records, and order the FDA to disclose all responsive records, including those it claims are exempt from disclosure.
“Given the FDA’s actions to publicize its decision, it should not be permitted to hide its supporting work in the shadows,” lawyers for the company wrote in the lawsuit.
“The public deserves a complete picture of the scientific facts behind one of the agency’s most controversial and closely scrutinized decisions in recent years, especially where even the FDA recognizes its order is suspect,” lawyers wrote.
‘Inequitable Treatment’
In Tuesday’s lawsuit, Juul said it submitted premarket tobacco product applications (PMTAs) to the FDA for its e-cigarette products as well as a new device with age-verification technology in July 2020.Juul said the PMTAs included “over 125,000 pages of data, information, and analysis from over 110 scientific studies to support the marketing of JUUL products.”
The company said the PMTAs aimed to show the FDA that following a “holistic analysis across multiple scientific disciplines,” its products would “reduce harm from tobacco use and that marketing them would be appropriate for the protection of public health.”
“This action will help us obtain information about the FDA review of our applications relevant to our continued appeal of the agency’s decision,” the spokesperson added.
An FDA spokesperson told The Epoch Times by email: “The FDA declines to comment on possible, pending, or ongoing litigation.”