Nonpartisan civic infrastructure
AllCiv·Legis1
·

H.R. 8202

BillFederalHouseIntroduced
To amend the Federal Food, Drug, and Cosmetic Act to require a recall of electronic nicotine delivery systems that have not been subject to premarket review, and for other purposes.
About This Bill
Introduced
Congress
117th (2021–2023)
Introduced
June 23, 2022
Cosponsors (0)
None
View PDF ↗

Summary

Highlight any text to annotate
Preventing Vape Use Act This bill requires electronic nicotine delivery systems (e.g., e-cigarettes and vape pens) to successfully undergo Food and Drug Administration (FDA) premarket review before being introduced into interstate commerce for commercial distribution. It also requires the FDA to order a mandatory recall of any such systems that have not successfully undergone premarket review.

Take Action

Your position
Add a comment
to comment on this bill.
Annotate the text
Highlight any passage on the Summary or Full Text tab to attach a note. Annotations appear on the Annotations tab.