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Shenzhen Kanger Technology Co. Ltd. d/b/a Kangertech was warned for offering electronic nicotine delivery system (ENDS) products for sale in the United States without premarket marketing authorization from the FDA. The company's products violated the Family Smoking Prevention and Tobacco Control Act by failing to obtain required authorization as "new tobacco products" and were found to be adulterated and misbranded. The FDA's jurisdiction was clarified to extend to all products containing nicotine from any source, not just tobacco-derived nicotine, following legislation signed in March 2022 that expanded regulatory authority.