CTA! Call to Action

The vaping industry needs your help to educate and get active in doing so. 

Most importantly, when we ask you to email and call your representatives - DO IT! They need to hear from YOU - the tax payer, the people involved when considering public health. Don't just assume others will do it. Please, make the time, tens of millions of lives rely on your efforts. It takes a village!


Anytime there is a Call to Action (CTA), CASAA already has a message tailored to each of the receipients. BONUS: There's a bigger impact if you share your testimony or your loved ones testimony in these messages.

We have the CTA headers in red. There may be more than one going on. We will post CTA's that concern Minnesota, North Dakota, Wisconsin, and the entire nation as a whole.

It takes less than 2 minutes
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Scroll down to read more on these call to actions!

National Call To Action – Light Up The White House Switchboard

On Wednesday, September 11, 2019, Donald Trump, along with HHS secretary Alex Azaar, announced that the administration would be banning all flavored vapor products from the market. In spite of an incredible 28% decline in youth smoking–according to early data from the National Youth Tobacco Survey (NYTS)–the administration is citing a 25% increase in vaping among young people as justification for taking such an extreme action.

The White House needs to hear from adult vapers and anyone who loves a vaper! A flavor ban won’t protect our children, but it will kill their parents.

We need to
Light Up The Switchboard
At The Whitehouse!
Ph: 202-456-1414

On your call:

  • The operator will likely ask where they can direct your call
  • Simply tell them that flavored vapor products saved your life; and,
  • tell them “We Vape, We Vote.

Be polite, be brief, and say thank you.


Do you want timely alerts about this issue and information about how you can do more?



Vaping Prohibition is On the Table in Congress!

In July, a US District Court judge, Paul Grimm, produced a remedy order that requires the FDA to enforce the premarket tobacco application (PMTA) requirement starting in May of 2020. This effectively moves up this particular compliance deadline by more than a year. While a small handful of companies might be in a position to attempt compliance with this new deadline, the rest of the vapor industry is not.

Strict enforcement of this deadline will force most US manufacturers to shut down. Even though the FDA will retain enforcement discretion with regard to certain compliance deadlines on a case-by-case basis, it is not clear how (or even if) the agency will apply it. In other words, there is no guarantee that companies will be allowed to keep their products on the market.

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At the same time, several bills are active in Congress that would undermine FDA’s authority over new tobacco products. These bills propose to raise taxes, ban flavors, limit online sales, and one bill even goes as far as requiring vapor products to be approved for market only as medical drugs/devices.

CASAA is asking our members to take action by sending a message to your federal lawmakers urging them to reject this legislation and prevent a massive underground market from taking the place of our current legal, regulated marketplace. We will start delivering your messages one week from now to coincide with a lobby day organized by the Vapor Technology Association.

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The long version:

By way of background, In July, Judge Paul Grimm, US District Court District of Maryland, ruled that the FDA has until May 2020 to enforce the premarket tobacco application (PMTA) requirement for new tobacco and vapor products.

The initial compliance deadline for PMTA was August 8, 2018. But in July 2017, the FDA delayed the PMTA deadline to 2022–for non-combustible products–citing a need to give vapor manufacturers more time to prepare and submit meaningful applications that would be more likely to be accepted by the agency.

Within a year, the FDA changed course after reviewing national survey data showing a sharp uptick in youth use of vapor products. The updated guidance would require applications to market vapor products in flavors other than tobacco to be submitted and accepted by the FDA by August of 2021. Although never finalized, the draft guidance would have also limited sales of flavored vapor products to adult-only specialty vapor/tobacco stores.

In 2018, the American Academy of Pediatricians (AAP) sued the FDA with the goal of reinstating the original August 8, 2018 PMTA compliance deadline. Following an exchange of proposed remedy briefs by both parties, Judge Grimm ruled that FDA’s suggestion of no less than ten months from the date of the court’s decision would be necessary for companies to finalize and submit acceptable applications. Judge Grimm granted FDA’s request.

The ten-month deadline is one of four points detailed in Judge Grimm’s remedy order. The remaining provisions of the order are as follows:

  • New products for which applications have not been filed within this period shall be subject to FDA enforcement actions, in the FDA’s discretion;
  • New products for which applications have been timely filed may remain on the market without being subject to FDA enforcement actions for a period not to exceed one year from the date of application while FDA considers the application;
  • The FDA shall have the ability to exempt New Products from filing requirements for good cause on a case-by-case basis.

While the one-year “grace period” for a manufacturer to keep a product on the market during FDA’s review of their application is nothing new, the points regarding the agency’s enforcement discretion and ability to exempt new products from the filing requirements are significant.

It may be hard to believe, but FDA specifically asked the court to preserve the agency’s enforcement discretion citing negative consequences of a mass exodus from the vapor market and an extreme and sudden decrease in access to safer alternatives to smoking. The FDA expressed strong concern that such an event would cause thousands of people who vape to return to smoking.

Preserving FDA’s enforcement discretion is not a free pass for the vapor industry and consumers should be very concerned about what this remedy order means for our access to vapor shops, vapor products, and other resources. The FDA and Congress are still facing tremendous pressure from anti-nicotine activists to ban flavors, enact taxes on vapor products, ban online sales, and raise the purchase age to 21. Additionally, we are monitoring a budding movement by local governments in California to take matters into their own hands by requiring that a vapor company has a marketing order from the FDA in order to sell their product in their city.

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If you aren't already, become a member of CASAA! It's free, although, donations towards the endless things they do to help the ease of getting you, the consumer, involced is appreciated. JOIN THE FIGHT. JOIN CASAA

The Consumer Advocates for Smoke-free Alternatives Association (CASAA) is a non-profit 501(c)(4) organization with an all-volunteer board and a grassroots membership of more than two hundred thousand individuals from all walks of life, and we are growing daily.  We are a consumer organization, not a trade association.  We are dedicated to ensuring the availability of reduced harm alternatives to smoking and to providing smokers and non-smokers alike with honest information about those alternatives so that they can make informed choices.