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.
Analysis under review: This bill has generated analysis that may be too generic or incomplete. Clause-level evidence remains available below.
Summary
What This Bill Does
This bill, 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., changes federal law or congressional policy affecting importers, exporters, and commercial firms. The main policy domain is Trade, Healthcare, Environment.
Who Benefits and How
importers, exporters, and commercial firms may benefit from new authority, funding, eligibility, regulatory clarity, or reduced risk created by the bill.
Who Bears the Burden and How
federal implementing agencies, importers, exporters, and commercial firms may take on implementation duties, reporting obligations, compliance costs, or oversight responsibilities.
Key Provisions
- Section HC91E84C239AF47DAB324EAD111BB0394: 1. Short title This Act may be cited as the Preventing Vape Use Act.
- Section HA38CC1A5B42A41E8AC03B6CA00D871D7: 2. Inclusion of ENDS in definition of tobacco product Section 201(rr)(1) of the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 321(rr)(1)) is amended by...
- Section H8FAE2578DFA84061AC419C8274793ADF: 3. Mandatory recall of ENDS pending premarket review Section 908(c) of the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 387h(c)) is amended by adding at the...
- Section H4C1FEFC063664A62BFEF4E963806BC2A: 4. No exemptions allowed for ENDS Section 910(a) of the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 387j(a)) is amended— in paragraph (2), by adding at the...
Evidence Chain:
This summary is generated from the full bill text using AI analysis. Expand "Detailed Analysis" below for identified beneficiaries/burden bearers with clause-level evidence links.
At a Glance
What This Bill Does
This bill, 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., changes federal law or congressional policy affecting importers, exporters, and commercial firms.
Key Policy Areas
Trade, Healthcare, Environment
Primary Purpose
This bill, 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., changes federal law or congressional policy affecting importers, exporters, and commercial firms.
Policy Domains
Whole bill
Identified Gains
- importers, exporters, and commercial firms
Identified Costs
- federal implementing agencies
- importers, exporters, and commercial firms
Legislative Progress
IntroducedMr. DeSaulnier introduced the following bill; which was referred to …
Impact analysis is available but no clear stakeholder effects identified. View clause-level analysis →
Bill Structure & Actor Mappings
Who is "The Secretary" in each section?
- "the_secretary"
- → The Secretary identified in the operative section
We use a combination of our own taxonomy and classification in addition to large language models to assess meaning and potential beneficiaries. High confidence means strong textual evidence. Always verify with the original bill text.
Learn more about our methodology