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This bill amends the Federal Food, Drug, and Cosmetic Act to require the FDA to mandate a recall of all electronic nicotine delivery systems (vaping products) that have not undergone premarket review, and to eliminate exemptions that would allow such products to be marketed without FDA approval. The bill defines electronic nicotine delivery systems broadly to include e-cigarettes, vape pens, and related devices, and requires manufacturers and distributors to cease distribution and recall products within a specified timeframe, with an opportunity for an informal hearing.
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