A House subcommittee on Wednesday will question the Food and Drug Administration’s (FDA) tobacco center director over the status of the Trump administration’s pledge to ban flavored e-cigarette products amid a growing epidemic of young users.
Mitch Zeller, the director of the FDA’s Center for Tobacco Products, is set to appear as a witness during the hearing.
The hearing follows subcommittee Chairman Rep. Raja Krishnamoorthi’s (D-Ill.) November letter to the White House and FDA in which he demanded to know the status of the proposed vaping-flavor guidance.
His letter followed numerous reports that Trump had backed off his pledge after pushback from the vaping industry and political advisers.
In September Trump and Health and Human Services Secretary Alex Azar announced that the FDA intended to finalize a guidance that would require all non-tobacco flavored vaping products to be removed from the market.
At the time of the announcement, Azar said 8 million adults and 5 million minors are using e-cigarettes. The Centers for Disease Control reported 2,290 cases of e-cigarette or vaping-associated lung injury and 47 confirmed deaths as of Nov. 20.
The White House Office of Management and Budget completed regulatory review of a proposed rule about “electronic nicotine delivery systems” on Nov. 4, and canceled meetings with public health advocates as well as pro-vaping groups, but the rule was never published.
Senators similarly pressed Zeller last month for information on the administration’s efforts to remove the products from the market, but he said he could not give them a timeline and directed questions on the announcement to the White House.
A White House spokesperson was not immediately available for comment.