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For ENDS products that fall in these categories, due to rising concerns of youth use, FDA published an Enforcement Priorities Guidance ending the compliance policy on February 6, 2020.[14] In other words, a cartridge or pod-based ENDS that comes in flavors other than tobacco or menthol can only be marketed today if it has obtained PMTA marketing authorization

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However, it is also expected that the rates of pneumothorax and the requirement for chest catheter drainage would also increase because of the prolonged needle indwelling time