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Tobacco Vapor Zone was cited for selling electronic nicotine delivery system (ENDS) products without the required premarket authorization orders mandated by the Family Smoking Prevention and Tobacco Control Act. The FDA determined that the company's products, which contain nicotine from any source, qualify as tobacco products subject to FDA jurisdiction and must comply with Federal Food, Drug, and Cosmetic Act requirements, including obtaining marketing authorization for any new or modified tobacco products. The warning specifically noted that as of March 15, 2022, FDA's jurisdiction expanded to include all products containing nicotine from any source, not solely those derived from tobacco, requiring full compliance with applicable regulations.