China Discloses First Criminal Case Over Counterfeit Vapes Disguised as “Medical Nebulizers” and “Zero-Nicotine” Products

Aug.04
China Discloses First Criminal Case Over Counterfeit Vapes Disguised as “Medical Nebulizers” and “Zero-Nicotine” Products
Chinese authorities have disclosed the country’s first reported criminal case involving counterfeit vapes marketed as “medical nebulizers” and “zero-nicotine” products. Authorities determined that the products involved were counterfeit vapes and pursued criminal charges for producing and selling counterfeit goods. According to the report, the case resulted in the seizure of 347,000 counterfeit vape pods and 53,700 vape devices, with physical goods valued at 22.13 million yuan.

Key Points

  • China disclosed its first reported criminal case involving “zero-nicotine” counterfeit vapes prosecuted under counterfeit goods laws.
  • Products were marketed as “medical nebulizers,” “zero-nicotine” and “additive-free” products.
  • Beijing tobacco authorities and police uncovered a cross-province illegal production and distribution network.
  • Authorities seized 347,000 counterfeit vape pods and 53,700 devices.
  • Nineteen people were criminally detained, nine arrested and two sentenced.

2Firsts

August 4, 2026

According to Beijing Daily’s “Legal Affairs in Progress” program on August 3, 2026, Beijing tobacco authorities, police and related departments disclosed a criminal case involving vape products disguised as “medical nebulizers” and “zero-nicotine” products.

Authorities determined that the products involved were counterfeit vapes and pursued criminal charges for producing and selling counterfeit goods.

The report described the case as China’s first judicial case involving the production and sale of “zero-nicotine” counterfeit vapes prosecuted under counterfeit goods laws.

The investigation uncovered a cross-province supply chain involving manufacturing, branded packaging and regional distribution.

Products Marketed as “Medical Nebulizers” and “Zero-Nicotine” Items

In late November 2024, the Shunyi District Tobacco Monopoly Bureau in Beijing received a public report alleging that a store in a shopping mall was selling vape products to minors.

Investigators found that the store sold multiple aerosol products, while product packaging and displays did not use the term “vape” or “electronic cigarette.”

Instead, products were promoted as:

  • “zero-nicotine” products;
  • “additive-free” products;
  • “medical heating nebulizers.”

The store also provided certain medical device and food-related qualifications, while its business registration did not include electronic cigarette-related activities.

According to the report, investigators examined whether aerosol products marketed under medical or food-related names could avoid vape regulation because they did not contain nicotine or used different product descriptions.

The report said that vape classification depends on product function and structure rather than nicotine content alone.

The products involved in the case were classified by authorities as counterfeit vapes.

Beijing Authorities Trace Cross-Province Illegal Supply Chain

After identifying the retail outlet, investigators traced the source of the products.

The investigation found that the operators were connected to a broader distribution network.

The supply chain reportedly involved:

  • contract manufacturing in Guangxi;
  • branded packaging in Guangdong;
  • regional distribution in Beijing;
  • concealed retail sales.

Authorities said the products were distributed through disguised names and packaging intended to avoid consumer and regulatory recognition.

In January 2025, Shunyi District Tobacco Monopoly Bureau, police and market supervision authorities conducted enforcement operations against the related locations.

Between May and June 2025, multiple departments carried out three rounds of cross-province operations.

Seizure of 347,000 Pods and Criminal Prosecution

According to the report, authorities seized:

Item

Quantity

Counterfeit vape pods

347,000

Vape devices

53,700

Physical goods value

22.13 million yuan

Case progress:

Status

Number

Criminally detained

19 people

Arrested

9 people

Sentenced

2 people

The report said the case dismantled a counterfeit vape production and distribution chain involving manufacturing outside Beijing, branded packaging and regional sales.

China’s Regulatory Approach Focuses on Product Characteristics

The case highlights China’s approach to evaluating vape products based on actual characteristics rather than product names alone.

The products involved were marketed using descriptions including:

  • “medical nebulizers”;
  • “zero-nicotine”;
  • “herbal” products.

However, according to the report, authorities considered product functions, structures and sales activities when determining regulatory classification.

For the vape industry, the case indicates that product classification may depend not only on marketing descriptions or nicotine content, but also on actual product features and intended use.

Follow 2Firsts for the latest updates on global tobacco and nicotine regulation, industry developments and market trends.

Cover Image source: Beijing Daily


Disclaimer

This article is provided solely for professional research, industry discussion, and informational purposes. Any references to brands, companies, products, technologies, or policies are made for factual reporting and analytical purposes only, and do not constitute endorsement, recommendation, promotion, or advertising by 2Firsts.

Nicotine-containing products, including but not limited to cigarettes, e-cigarettes, heated tobacco products, and nicotine pouches, carry significant health risks. Readers are responsible for complying with all applicable laws and regulations in their respective jurisdictions, including age restrictions and access limitations.

The information contained in this article should not be regarded as investment, legal, medical, regulatory, or commercial advice. While 2Firsts strives to ensure the accuracy and reliability of its content, it does not assume liability for any direct or indirect loss arising from errors, omissions, inaccuracies, or reliance on the information contained herein.

This article is not intended for individuals below the legal age for accessing tobacco or nicotine-related information in their jurisdiction.

 

Copyright Notice

This article is either original content produced by 2Firsts or content reproduced, translated, summarized, or adapted from third-party sources with attribution where applicable. The intellectual property rights of the original content remain with 2Firsts or the respective original rights holders.

No individual or organization may copy, reproduce, distribute, republish, modify, translate, or otherwise use this content without prior authorization. Any unauthorized use may result in legal action.

For copyright-related inquiries, corrections, or removal requests, please contact: info@2firsts.com.

 

AI-Assisted Translation and Editing Notice

Portions of this article may have been translated, edited, or reviewed with the assistance of artificial intelligence tools to improve efficiency and readability. Due to the limitations of AI-assisted translation and editing, discrepancies, omissions, or inaccuracies may exist when compared with the original source.

Where applicable, readers are advised to refer to the original source for the most complete and accurate information. If you identify any errors or believe that any content infringes upon your rights, please contact us at info@2firsts.com, and we will review and address the matter promptly.

Kantar Study Finds More Than 93% of Vape Products in Ukraine Fail Regulatory Requirements
Kantar Study Finds More Than 93% of Vape Products in Ukraine Fail Regulatory Requirements
According to Interfax-Ukraine, a study conducted by market research firm Kantar Ukraine at the request of major tobacco companies found that more than 93% of vape products in Ukraine did not fully comply with regulatory requirements. The research examined product categories, brand distribution and consumer purchasing channels, showing that pod systems and disposable vapes represent major segments of the market, while offline retail remains the dominant purchasing channel. The findings highlight ongoing compliance challenges in Ukraine’s vape market.
Aug.26
Philippines Customs Seizes PHP11.68 Billion($200 Million) in Illegal Tobacco and Vapes in First Seven Months of 2026
Philippines Customs Seizes PHP11.68 Billion($200 Million) in Illegal Tobacco and Vapes in First Seven Months of 2026
Philippines Customs data showed that illegal cigarettes and vape products seized during the first seven months of 2026 were valued at about PHP11.68 billion, exceeding the PHP2.516 billion recorded for the full year of 2025. The figures were disclosed by a Bureau of Customs official during a House Committee on Ways and Means hearing on tobacco excise tax reforms. Vape-related seizures were valued at about PHP1.65 billion, with most cases recorded at the Manila International Container Port. Customs officials said enforcement against illicit tobacco trade would continue.
Aug.26
FDA Authorizes JUUL2, Cites Adult Switching Amid Efforts to Speed PMTA Reviews
FDA Authorizes JUUL2, Cites Adult Switching Amid Efforts to Speed PMTA Reviews
The FDA authorized the JUUL2 device and tobacco- and menthol-flavored pods on Aug. 28, bringing the number of authorized e-cigarette products to 48. The agency highlighted complete switching among adult smokers, with six-week switching rates reaching 28.4%–49.3% for the menthol pod. The decision comes as FDA works to speed PMTA reviews, reduce application backlogs and expand authorized e-cigarette and nicotine-pouch products while maintaining enforcement priorities for unauthorized products.
Regulations
Aug.29
FDA Authorizes Four More Nicotine Pouches as Review Pilot Expands Beyond Initial Decisions
FDA Authorizes Four More Nicotine Pouches as Review Pilot Expands Beyond Initial Decisions
The FDA has authorized four additional on! nicotine pouches, bringing the U.S. total to 30. The decision marks another outcome of the agency’s nicotine pouch review pilot, whose communication and review practices are now being applied more broadly across the category. It also extends Helix’s authorized portfolio from on! PLUS to the earlier on! line. Yet all FDA-authorized nicotine pouches still come from subsidiaries of PMI or Altria, underscoring how concentrated U.S. regulatory access remains.
Aug.05
STIIIZY Redesign Fails to Escape PAX Labs Patent Import Ban as Section 337 Case Also Involves China ALD
STIIIZY Redesign Fails to Escape PAX Labs Patent Import Ban as Section 337 Case Also Involves China ALD
U.S. Customs and Border Protection ruled that STIIIZY had not shown that the redesigned cannabis-vape products covered by its latest request fall outside an ITC limited exclusion order tied to PAX Labs patents. CBP accepted some of STIIIZY’s claim-construction and non-infringement arguments, but the company did not address two additional claims in the same patent. Earlier STIIIZY redesigned cartridges and certain associated components imported with them had received separate CBP clearance.
Sep.16
As JUUL2 Wins FDA Authorization, Harm Reduction Journal Highlights the Role of Real-World Evidence in Nicotine Product Regulation
As JUUL2 Wins FDA Authorization, Harm Reduction Journal Highlights the Role of Real-World Evidence in Nicotine Product Regulation
A commentary published in the international open-access, peer-reviewed Harm Reduction Journal argues that randomized controlled trials remain central to evaluating smoking cessation efficacy but cannot alone capture real-world uptake, complete switching, longer-term use and population impact of non-combustible nicotine products such as e-cigarettes, heated tobacco and nicotine pouches. The authors frame impact as “reach × efficacy” and call for real-world evidence to complement RCTs. Three days after publication, the FDA authorized three JUUL2 products and highlighted complete switching among adult smokers in explaining its decision, providing a timely regulatory backdrop to the debate.
Sep.08