The FDA’s strategy on vaping is going up in smoke — now Americans are put at risk

Published



The Food and Drug Administration is hoping to take a page out of John Kerry’s flip-flopping playbook. While running for president in 2004, Kerry tried to explain his blatant inconsistency on a spending bill by saying he was for it before he was against it. Kerry’s attempt at rhetorical origami didn’t work then, and it won’t work for the FDA now.

Under federal law, tobacco and vaping products are not to be sold until they have been reviewed and authorized by the FDA. That requirement isn’t unreasonable, especially since Congress directed — not asked — the FDA to act on applications within 180 days. But during the Biden administration, the FDA essentially stopped reviewing tobacco and vape products, ballooning the average review to nearly 1,000 days from the date an application is submitted. The Trump administration inherited that backlog, and the president is trying to fix it.

Full midterm coverage.Deeper analysis.

Get unlimited access to Washington Examiner's reporting, expert analysis, and coverage of the midterm elections.

Get Unlimited Access

Cancel anytime.