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Dispo Mode was warned for offering electronic nicotine delivery system (ENDS) products for sale in the United States without required premarket authorization. The company's products, which contain nicotine and fall under FDA's tobacco product jurisdiction, failed to comply with section 910 of the Federal Food, Drug, and Cosmetic Act, which requires new tobacco products to obtain a marketing authorization order before being legally marketed. The warning was issued following FDA's review of the company's website (dispomode.com) and reflected the expanded FDA jurisdiction over all nicotine-containing products, including those with non-tobacco-derived nicotine, effective as of April 14, 2022.