SOURCE: FDA

January 29, 2021

Today FDA released an additional 9 warning letters to companies making and selling unauthorized electronic nicotine delivery system (ENDS) products without having submitted corresponding PMTA’s by the September 9, 2020 deadline. FDA informed these manufacturers that the making and selling of these products without premarket authorization is illegal and these products must be pulled from market immediately. The warning letters issued today follow a series of warning letters that were distributed earlier this month, signaling the start of FDA enforcement of PMTA regulation for the ENDS industry. With this newest series of letters, the total number of warning letters issued to date has now reached 20.

CLICK HERE for the full list of current warning letters from the FDA