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Mandatory Recall of Vapes Without Prior Government Approval

New regulations mandate the immediate recall of all electronic nicotine delivery systems (ENDS) that have not undergone prior government review before being placed on the market. This means many currently available vape products may be removed from shelves, and manufacturers will need to obtain specific authorizations to sell them again. The aim is to enhance the safety of electronically delivered nicotine products.
Key points
All vape products that have not received premarket authorization must be recalled from the market within 60 days of the act's enactment.
Electronic nicotine delivery systems (ENDS) are now officially included in the definition of tobacco products, subjecting them to stricter regulations.
Manufacturers, importers, distributors, and retailers are required to immediately cease distribution and recall affected products.
Simplified premarket review exemptions based on substantial equivalence to existing products will no longer apply to ENDS.
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Expired
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Additional Information
Print number: 117_HR_8202
Sponsor: Rep. DeSaulnier, Mark [D-CA-11]
Process start date: 2022-06-23
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Summarized by: gemini-2.5-flash
Source data: api.congress.gov
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OFFICIAL LEGAL TITLE

Preventing Vape Use Act

FREQUENTLY ASKED QUESTIONS

What is the official ID of this bill?

The official print number for this legislation is 117_HR_8202.

Which chamber initiated this legislation?

This legislation was initiated in the House of Representatives.

When did the legislative process begin?

The process officially started on 2022-06-23.

What are the main provisions?

Key points include:

  • All vape products that have not received premarket authorization must be recalled from the market within 60 days of the act's enactment.
  • Electronic nicotine delivery systems (ENDS) are now officially included in the definition of tobacco products, subjecting them to stricter regulations.
  • Manufacturers, importers, distributors, and retailers are required to immediately cease distribution and recall affected products.
  • Simplified premarket review exemptions based on substantial equivalence to existing products will no longer apply to ENDS.
What is the specific legal status?

The current status is Expired.

Where can I read the full text of this legislation?

The full official text is available at: View full text

Who is the primary sponsor?

The primary sponsor is Rep. DeSaulnier, Mark [D-CA-11].

What is the latest detailed status?

The latest detailed status is: Referred to the House Committee on Energy and Commerce.

Is this summary verified?

Yes. This content was analyzed by AI and verified by the Lustra Judge System on 2026-01-02.

CATEGORIES

Health