| In August, FDA issued the first marketing denial orders (MDOs) for electronic nicotine delivery system (ENDS) products. As of now, the agency has issued a total of 295 MDOs for more than 1,089,000 flavored ENDS products. Products subject to an MDO for a premarket application may not be introduced or delivered for introduction into interstate commerce. If the product is already on the market, the product must be removed from the market or risk enforcement. Companies receiving these MDOs may have submitted premarket applications for other products (such as ENDS devices, tobacco-flavored ENDS, or menthol-flavored ENDS), and those products, if still pending, remain under review at FDA. | | | |
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