President Trump tries to save vaping
Health Care Newsletter
President Trump tries to save vaping
by Nathaniel Weixel and Joseph Choi - 05/06/26 6:17 PM ET
Link copied
by Nathaniel Weixel and Joseph Choi - 05/06/26 6:17 PM ET
Link copied
96
- Click in for more news from The Hill
{beacon}
Health Care
Health Care
 
The Big Story
President Trump tries to save vaping
The Trump administration handed e-cigarette companies a win this week when it authorized the sale of blueberry and mango flavored nicotine vaping pods, as well as two menthol flavored products. It was the first time the agency has greenlit a fruit-flavored electronic cigarette product.
© Greg Nash
The announcement came just hours after it was reported that President Trump pressured Food and Drug Administration Commissioner Marty Makary to make the move. In the runup to the 2024 election, Trump vowed to “save” vaping.
It marks a significant shift for the FDA, which had previously turned away applications for more than 1 million fruit, candy and dessert-flavored products. The agency to date has authorized only a few dozen flavored vaping products, and all except one have been tobacco flavored, which is not widely used by young people.
Some public health experts and anti-smoking groups worry that fruity flavors will entice children; they point to the Juul-fueled vaping crisis, driven by the product’s fruity flavors when it first came on the market.
But youth vaping rates have significantly declined in recent years, and the legal age to purchase tobacco is now 21. And there is research showing vaping can help smokers transition away from traditional cigarettes, though e-cigarettes are not without health risks.
In its announcement, the FDA reasoned that the products manufactured by Glas Inc. will prevent young people from accessing the vapes while also helping adults quit cigarettes.
The company’s age gate technology requires Bluetooth connection to a smartphone as well as age verification with an uploaded government ID. The device won’t work unless it is close to the phone it’s paired with.
“By helping to prevent youth use, device access restrictions are a potential game changer,” Bret Koplow, acting director of the FDA’s Center for Tobacco Products, said in a statement.
“This technology is also an indication of the role innovation may serve in the effort to protect young people from threats posed by nicotine use and addiction while helping to enable availability of an expanded array of flavored options for adults who smoke who may use these products to completely switch away from regular cigarettes.
 
Welcome to The Hill’s Health Care newsletter, we’re Nathaniel Weixel and Joseph Choi — every week we follow the latest moves on how Washington impacts your health.
 
Did someone forward you this newsletter? Subscribe here.
 
Essential Reads
How policy will be impacting the health care sector this week and beyond:
 
New surgeon general pick in deleted posts criticized Trump, RFK Jr. policies
President Trump’s nominee for surgeon general, Nicole Saphier, previously criticized healthcare guidance and recommendations from the administration in now-deleted social media posts unearthed by CNN. Saphier, a former Fox News contributor and radiologist, seemed less than impressed in archived posts on the social platform X when it came to some aspects of how the White House was handling infectious disease and medical …
Full Story
 FDA stopped publication of studies showing COVID, shingles vaccines were safe
The Food and Drug Administration (FDA) in recent months stopped publication of studies about the safety of COVID-19 and shingles vaccines, a spokesperson for the Department of Health and Human Services confirmed. “The studies were withdrawn because the authors drew broad conclusions that were not supported by the underlying data,” spokesperson Andrew Nixon said. “The FDA acted to protect the integrity of …
Full Story
 UnitedHealthcare to eliminate prior authorization for 30 percent of services
(NewsNation) — UnitedHealthcare plans to eliminate prior authorization for 30 percent of services that require insurer approval, reducing delays and paperwork for patients and doctors. The company said, by the end of 2026, it will remove prior authorization requirements for certain outpatient surgeries, diagnostic tests such as echocardiograms, and some outpatient therapies and chiropractic care. Prior authorization is a process …
Full Story
 
 
In Other News
Branch out with a different read:
FDA approves some flavored vapes after reports of Trump pressure
The Food and Drug Administration (FDA) on Tuesday approved marketing for four flavored vapes made by the company Glas Inc. in what the agency says is an effort to tamp down on underage use of these products. The FDA said the prod