Federal Judge Allows Collective Lawsuit Against Juul Marketing

Jun.30.2022
Federal Judge Allows Collective Lawsuit Against Juul Marketing
A US federal judge allows collective lawsuits against Juul, accusing the company of misleading marketing and demanding compensation for its purchasers.

A federal judge has permitted both adult and underage individuals who have purchased Juul e-cigarettes to file a collective lawsuit, demanding compensation from the company for deceptive marketing practices.

 

On Tuesday, U.S. District Judge William Orrick certified four groups, consisting of adults and minors both nationwide and in California, but rejected arguments made by Juul and its largest shareholder, tobacco giant Altria Group Inc., stating that the potential members of the collective were too diverse to bring a lawsuit for their claims together.

 

These class-action lawsuits do not accuse the product of causing bodily harm, but rather demand a refund of the money spent on purchasing Juul products.

 

The above is part of the multi-district litigation being handled by Orrick, which includes personal injury claims and lawsuits brought by local governments and school districts alleging that Juul fueled an epidemic of youth addiction.

 

Lawyers for plaintiffs Juul and Altria did not immediately respond to requests for comment.

 

The economic loss claims allege that Juul downplayed the addictive nature of its products and, had it not been for deceptive marketing, consumers would not have purchased these products or would have spent less money on them.

 

Juul argues that they should not be classified as a class-action lawsuit because different consumers were exposed to different advertisements, and some individuals became addicted while others did not.

 

However, Orrick believes that these differences are "largely immaterial under the legal theory being asserted.

 

Under pressure from regulators, Juul removed popular flavors such as mango and cucumber from retail stores in 2018 and closed its social media channels on Instagram and Facebook.

 

Earlier this month, the US Food and Drug Administration (FDA) ordered the removal of all Juul e-cigarettes from the market, but this decision was temporarily halted by the federal appeals court.

 

Juul has agreed to pay over $87 million to settle charges related to its marketing of products to minors with four states.

 

Source: Reuters

 

This document has been generated through artificial intelligence translation and is provided solely for the purposes of industry discourse and learning. Please note that the intellectual property rights of the content belong to the original media source or author. Owing to certain limitations in the translation process, there may be discrepancies between the translated text and the original content. We recommend referring to the original source for complete accuracy. In case of any inaccuracies, we invite you to reach out to us with corrections. If you believe any content has infringed upon your rights, please contact us immediately for its removal.

2Firsts|Sesh Advances Nicotine Pouch PMTA to Filing Stage, Experts Highlight Regulatory Threshold and Market Window
2Firsts|Sesh Advances Nicotine Pouch PMTA to Filing Stage, Experts Highlight Regulatory Threshold and Market Window
Sesh said its Premarket Tobacco Product Application (PMTA) for 64 nicotine pouch SKUs has been accepted by the U.S. Food and Drug Administration (FDA) and advanced to the Filing stage, entering substantive scientific review. Industry experts say the development signals that the application has crossed a key technical and regulatory threshold, while also highlighting growing divergence in regulatory capability and market positioning within the nicotine pouch category.
Special Report
Mar.24 by 2FIRSTS.ai
Six Years of Data Show FDA Clearing PMTA Backlog
Six Years of Data Show FDA Clearing PMTA Backlog
FDA data from FY2020 to FY2025 show how the PMTA system for e-cigarette products evolved after an early surge of submissions created prolonged front-end delays. Millions of applications accumulated at the Acceptance stage before entering substantive review. Since 2023, the number of applications pending acceptance has declined sharply, and industry participants report shorter initial decision timelines in late 2025.
Feb.06
Special Report|From Nicotine Pouches to Jelly? A China Tobacco Patent Explores Dual-Release NRT
Special Report|From Nicotine Pouches to Jelly? A China Tobacco Patent Explores Dual-Release NRT
A patent published on February 24, 2026, by China Tobacco Hubei Industrial Co., Ltd. introduces a “nicotine jelly” product designed to combine rapid and sustained nicotine delivery. By integrating both free and microencapsulated nicotine, the product aims to address key limitations of traditional nicotine replacement therapy (NRT), while also raising new regulatory and product classification questions.
Innovation
Mar.18
West Virginia House passes “Vape Safety Act of 2026,” creating licensing and product directory requirements
West Virginia House passes “Vape Safety Act of 2026,” creating licensing and product directory requirements
West Virginia’s House of Delegates passed the Vape Safety Act of 2026, a proposal to tighten oversight of vape and smoke shops through licensing, fees and enforcement. The bill would establish a state directory requiring vape products sold in West Virginia to have FDA marketing authorization or a pending application under FDA review to be listed, and only directory-listed products could be sold starting Sept. 1, 2026 if enacted.
Feb.28 by 2FIRSTS.ai
PMTA Roundtable Opens with Industry Questioning Product Characterization Standards, FDA Defends Regulatory Boundaries
PMTA Roundtable Opens with Industry Questioning Product Characterization Standards, FDA Defends Regulatory Boundaries
At the opening of FDA’s PMTA roundtable, small ENDS manufacturers warned that unclear product characterization standards are limiting their ability to invest and raise capital. FDA officials acknowledged industry concerns but said regulatory flexibility is constrained by statutory and procedural boundaries.
Feb.11
UK Tobacco and Vapes Bill Enters House of Lords Report Stage
UK Tobacco and Vapes Bill Enters House of Lords Report Stage
The Tobacco and Vapes Bill has entered the report stage in the UK House of Lords, with further examination scheduled to begin on February 24, 2026. The legislation aims to create the first “smoke-free generation” by ensuring that individuals who are 15 years old or younger in 2026 can never legally be sold tobacco.
Regulations
Feb.22