TheFood and Drug Administration(FDA ) has announced that they will banish the sale of JUUL e - cigarettes . The FDA has issued amarketing denial order(MDOs ) to JUUL Labs Inc. This means that the company must stop distributing and selling these products , and any products that are on the market need to be removed or there will be an enforcement action .

The products that are included in this ban are the JUUL gadget and the four different types of JUULpods : menthol - flavored pods at nicotine concentrations of 5.0 percent and 3.0 pct and Virginia tobacco season seedcase at nicotine concentrations of 5.0 percent and 3.0 percent .

“ Today ’s action is further progress on the FDA ’s consignment to secure that all einsteinium - cigarette and electronic nicotine livery system products currently being marketed to consumer run into our public health standards,”saidFDA Commissioner Robert M. Califf , M.D.

“ The government agency has give significant imagination to review products from the companies that account for most of the U.S. market . We recognize these make up a significant part of the useable products and many have played a disproportional role in the rise in youth vaping . ”

How did it add up to this ?

After critique the company’spremarket tobacco product applications(PMTAs ) , it was determined by the FDA that these applications lacked sufficient evidence on the products ' toxicologic profile , and therefore the company could not demonstrate that marketing of the products would be appropriate for public health protection

There was also some business concern for the findings of the company ’s studies , which caused worries due to insufficient and contradictory information – especially regarding the potentially harmful chemicals that can strip from the proprietary e - liquid pods and their genotoxicity potential .

FDA cite that they had not received any clinical information to suggest that there is an contiguous hazard if someone uses these devices or pods . However , the MDOs has been issued as FDA can not ascertain the possible toxicological risks of using JUUL ware .

“ The FDA is task with ensure that tobacco plant product betray in this land meet the standard set by the natural law , but the responsibility to demonstrate that a product meets those standard ultimately fall on the shoulder of the fellowship , ” said Michele Mital , acting manager of the FDA ’s Center for Tobacco Products , in astatement .

“ As with all manufacturers , JUUL had the opportunity to provide evidence manifest that the merchandising of their Cartesian product meet these standards . However , the fellowship did not provide that evidence and instead forget us with significant questions . Without the data take to find out relevant health hazard , the FDA is issuing these marketing denial ordering . ”

The FDA also could not find the possible peril of using the other e - liquid pod with the JUUL twist , or frailty versa ( using JUUL pod with a non - JUUL gimmick ) .

The FDA also recommends that any user of the JUUL products that have any unexpected wellness or product problem report them to the FDA through theSafety Reporting Portal , and also seek aesculapian aid as necessary .

This tale will be updated as more data come in .