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FDA Inspection Blitz Leads to Over 180 Warning Letters to Retailers for the Sale of Unauthorized E-Cigarettes

By Azim Chowdhury & Amber Grover on June 30, 2023
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On June 22, 2023, FDA announced it had issued warning letters to 189 retailers for selling unauthorized flavored tobacco products manufactured by Elf Bar and Esco Bar brands. This enforcement action comes on the heels of earlier aggressive action by FDA in its issuance of more than 570 warning letters to firms for the manufacture, sale, or distribution of unauthorized tobacco products from January 2021 through May 2023.

In its press release, FDA highlighted two studies recently published in the CDC’s Morbidity and Mortality Weekly Report. The first study found that Elf Bar branded disposable e-cigarettes were the most popular disposable e-cigarette sold in the U.S. in 2022, and the second study showed thousands of e-cigarette exposure cases reported to U.S. poison control centers in the past year, most of which were among kids younger than five years old.

For context, according to the most recently published annual report from the National Poison Data System (NPDS) in 2021, there were 2,527,332 exposures reported to poison centers. The five products most frequently reported were analgesics (11.2%), household cleaning substances (7.49%), cosmetics/personal care products (5.88%), antidepressants (5.61%), and sedatives/hypnotics/antipsychotics (4.73%). Tobacco products (all categories) were identified in 0.51% of exposure cases, with nicotine-containing e-cigarettes representing 0.21% of all exposures. For children five years and younger, tobacco products accounted for 1.17% of exposures, with e-cigarettes representing 0.47% of all exposures.

As concerns over youth use of disposable ENDS such as Elf Bar continue to rise, the good news is that current (past-30 days) youth vaping rates appear to be falling. A group of public health experts working with Keller and Heckman recently filed a brief with the U.S. Supreme Court noting, among other things, that youth vaping has declined markedly since 2019.

To date, FDA has authorized only twenty-three tobacco-flavored e-cigarette products and devices and has either refused or denied Premarket Tobacco Product Applications (PMTAs) for over 26 million products, the vast majority of which are non-tobacco flavored. Only e-cigarettes subject to PMTA Marketing Granted Orders are authorized to be sold in the United States. Sales of unauthorized tobacco products are prohibited by the Food, Drug and Cosmetic Act and are subject to penalties, including warning letters, injunctions, product seizures, and/or civil monetary penalties. 

Photo of Azim Chowdhury Azim Chowdhury

Azim Chowdhury is a regulatory and public policy attorney with a focus on vapor, nicotine and tobacco product regulation. He is a Partner in Keller and Heckman’s nationally-ranked food and drug law practice.

Mr. Chowdhury advises domestic and foreign corporations in matters of…

Azim Chowdhury is a regulatory and public policy attorney with a focus on vapor, nicotine and tobacco product regulation. He is a Partner in Keller and Heckman’s nationally-ranked food and drug law practice.

Mr. Chowdhury advises domestic and foreign corporations in matters of Food and Drug Administration (FDA) and international regulatory compliance. In particular, he has developed expertise in tobacco and vapor product regulation relating to the implementation of the Family Smoking Prevention and Tobacco Control Act, and spearheaded the Tobacco and E-Vapor practice at Keller and Heckman. Specifically, Mr. Chowdhury has experience representing tobacco, e-cigarette and e-liquid manufacturers, distributors, retailers, suppliers and trade associations in matters of FDA, state and global regulatory compliance. He also assists corporations in establishing clearances for food and drug additives in the U.S., Canada, and European Union, with an emphasis on indirect additives used in food-contact materials.

Mr. Chowdhury has authored and edited numerous articles and publications, including Tobacco Regulation and Compliance: An Essential Resource, FDA Regulation of Tobacco: A Comprehensive Guide – An FDLI Primer and Tobacco and Nicotine Delivery: Regulation and Compliance, 2nd Edition. He is a frequent contributor to the Food and Drug Law Institute’s (FDLI) Update Magazine and has served on the Editorial Advisory Board of the Food and Drug Law Journal.  In addition, he has been interviewed in the U.S. News and World Reports Best Lawyers Edition (2016) and was named one of “10 Names to Know in the Vape World” in the October 2015 issue of Vape Magazine. Mr. Chowdhury received the 2018 National Law Review Go-To Thought Leadership Award for his consistent coverage of the emerging issues surrounding vaping and e-cigarettes on Keller and Heckman’s law blog, The Continuum of Risk.  As an industry leader, Mr. Chowdhury frequently speaks at industry conferences and events.

Mr. Chowdhury also has an active pro bono practice through Keller and Heckman’s Pro Bono Program, and has been featured in the Baltimore Sun for successfully obtaining asylum in the United States for a family who fled their home country of El Salvador because of violence they faced from an international gang.

Prior to entering private practice, he served as a judicial law clerk on the Court of Special Appeals of Maryland. Mr. Chowdhury received a B.A. and B.S. from Johns Hopkins University, a MBA from the University of Maryland Robert H. Smith School of Business, and a JD, cum laude, from the University of Maryland School of Law.

Education: Johns Hopkins University (B.A., B.S., 2003); University of Maryland Robert H. Smith School of Business (M.B.A., 2006); University of Maryland School of Law (J.D., 2006, cum laude).

Admissions: District of Columbia; Maryland

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  • Posted in:
    Food, Drug & Agriculture
  • Blog:
    The Continuum of Risk
  • Organization:
    Keller Heckman
  • Article: View Original Source

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