Criticism as Brian King Named Director of FDA Center for Tobacco Products

News
May.20.2022
Criticism as Brian King Named Director of FDA Center for Tobacco Products

Brian King, currently a higher-up at the Centers for Disease Control and Prevention (CDC) in Atlanta, will become the new director of the Food and Drug Administration’s Center for Tobacco Products (CTP), the FDA announced on May 20.

 

An epidemiologist, King has spent more than a decade at the CDC, most recently as the deputy director for research translation at the Office on Smoking and Health (OSH). He will assume his new role on July 3, 2022. His predecessor as permanent director, Mitch Zeller, retired in the spring after a contentious career; the CTP has since been headed by Michele Mital on an interim basis.

 

The news comes at a time when CTP still has to sort through many of the premarket tobacco product applications (PMTAs) from the largest vape manufacturers, and as the office has been under recent fire for poor public health communication about the relative risks of e-cigarettes and safer nicotine alternatives. The reaction among consumer advocates was mixed at best: Some expressed cautious optimism that an epidemiologist might understand the issues better than a lawyer like Zeller, while others feared this might be just a status-quo move—or worse.

 

Many observers have pointed to King’s botching, in his CDC role, of the lung illnesses—misleadingly dubbed “e-cigarette or vaping use-associated lung injury,” or EVALI—that cropped up in the summer of 2019. Three years later, the CDC has still failed to be explicit that the cases were only tied to vaping illicitly manufactured, adulterated THC cartridges—and not nicotine, as the agency originally implied.

 

“Brian King’s long history of obfuscation around the issue of tobacco harm reduction is hard to ignore.”

 

Criticism has also been levied at King’s past comments on e-cigarettes. He’s accused of having overemphasized the harms of vaping products among youth at the expense of their harm reduction role for adult smokers, and of fear-mongering—through claims that e-cigarettes could be modified to contain “heroin, methamphetamines, powdered cocaine, and bath salts.”

 

“While there is always value in optimism, Brian King’s long history of obfuscation around the issue of tobacco harm reduction is hard to ignore,” Greg Conley, the president of the American Vaping Association (AVA), told Filter. “In his role at the Office on Smoking and Health, King has ignored or downplayed CDC’s own surveys showing several million adult ex-smokers using vaping as a total alternative for smoking, while leaping at opportunities to make absurd claims about the impacts of youth vaping. We are hopeful the FDA’s hiring of an ideologue to act as a supposedly neutral regulator will lead to renewed interest in this issue by members of Congress.”

 

“Brian King is among the worst choices for CTP that exists,” an industry insider, who requested anonymity so as not to affect his company’s PMTAs, told Filter. “He has no understanding of tobacco harm reduction or the continuum of risk, and has demonstrated a fundamental misunderstanding of what an e-cigarette even is. I expect his reign to be plagued by litigation [and that he] never accomplishes any of his stated goals for the regulation of the industry.”

 

In a letter circulated to FDA staff, Robert Califf, the agency’s commissioner, lauded King on his expertise, writing that “he has an extensive and nuanced understanding of, and appreciation for the 2009 Family Smoking and Prevention Act, detailed knowledge of premarket review pathways, premarket tobacco product applications, substantial equivalence, and modified risk tobacco products, as well as experience in the interagency scientific review of regulatory documents related to tobacco product standards, testing and reporting of ingredients, and health information.”

 

King, for his part, is anxious to get started.

 

“There’s critical work to be done to further prevent people from starting to use tobacco products, encourage tobacco users to quit and reduce the harm caused by tobacco use,” King said in a press statement. “During my time at CDC, I’ve had the great privilege to work with the staff at the FDA’s Center for Tobacco Products on a number of important tobacco issues, and I’m excited to lead CTP to advance these efforts.”

 

Source:filtermag

Vuse Alto Adds New U.S. Price Tier as BAT Pushes Deeper Into Mass-Market Vaping
Vuse Alto Adds New U.S. Price Tier as BAT Pushes Deeper Into Mass-Market Vaping
British American Tobacco (BAT) subsidiary Vuse Alto has recently adjusted its price tiers in U.S. convenience store channels, leveraging low-cost device kits and pod promotions to reinforce its positioning in the mid-priced closed-system e-cigarette market.
Jun.17
Seita’s Julia Neumaier Says France Should Target Vape Access, Not Plain Packaging
Seita’s Julia Neumaier Says France Should Target Vape Access, Not Plain Packaging
Julia Neumaier, general manager of Seita, Imperial Brands’ French subsidiary, said France should focus vaping regulation on access control, age verification, online sales and distribution channels, rather than applying tobacco-style plain packaging to vaping products.
Jul.15
China’s Jiangsu Tobacco Monopoly Bureau and Drug Regulator Target Illegal Vape Sales Disguised as Medical Devices, Define Six Violations
China’s Jiangsu Tobacco Monopoly Bureau and Drug Regulator Target Illegal Vape Sales Disguised as Medical Devices, Define Six Violations
China’s Jiangsu Tobacco Monopoly Bureau and Jiangsu Provincial Medical Products Administration have issued a joint notice targeting illegal production and sales of vape products disguised as medical devices. The notice identifies six categories of violations, including obtaining medical licenses through false materials, misusing medical device credentials, expanding production beyond approved scopes, and using medical device-related online platforms to promote or sell vape products. The action is based on China’s tobacco and medical device regulations and aims to strengthen vape oversight and consumer protection.
Aug.04
Data|China’s January-May Vape Exports: U.S. Shipments Fall 13.8% as Japan Posts Fastest Growth
Data|China’s January-May Vape Exports: U.S. Shipments Fall 13.8% as Japan Posts Fastest Growth
According to China Customs export data analyzed by 2Firsts, the United States remained China’s largest destination for vape-related exports during January-May 2026 despite a 13.82% year-on-year decline in export value. Meanwhile, exports to Japan, Russia, Indonesia and the United Arab Emirates recorded strong growth, highlighting continued diversification across China’s export markets.
Special Report
Jun.29
Tobacco Companies Are Redesigning Nicotine Products. BAT Wins Three Red Dot Awards
Tobacco Companies Are Redesigning Nicotine Products. BAT Wins Three Red Dot Awards
According to BAT and the Red Dot Design Award website, BAT’s glo Hilo Plus, Vuse Pro One Box and Vuse Ultra x McLaren F1 Team Limited Edition received Red Dot recognition in the Product Design 2026 competition.BAT said the awards reflect not only the design quality of the individual products but also the development of design as a core internal capability across industrial design, user experience and sustainability. Red Dot’s product pages describe glo Hilo Plus as a two-part tobacco heater with a pen and charging case, plus a touch-sensitive AMOLED display. Vuse Pro One Box is described as a rechargeable e-cigarette with replaceable pods, USB-C charging and a switchable VapourBoost mode. Vuse Ultra x McLaren F1 Team Limited Edition brings motorsport-inspired design elements into a compact e-cigarette device and includes exchangeable batteries.
Jul.17
Indiana’s Foreign-Made Vape Ban Takes Effect, Forcing Brands and Retailers to Adjust Supply Chains
Indiana’s Foreign-Made Vape Ban Takes Effect, Forcing Brands and Retailers to Adjust Supply Chains
A new Indiana law restricting the sale of foreign-made vape products has taken effect, requiring retailers to adjust inventory and sourcing practices. According to The Sun, WDRB and other reports, some local vape shops are reviewing product origins and supplier information to comply with the new requirements. The measure represents a broader shift in U.S. vape regulation, with oversight expanding beyond product authorization and sales rules toward manufacturing origin and supply-chain management.
Jul.24