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More and more cases of e-cigarettes exploding without warning. The latest, a Phoenix-area man is severely burned when the vape device in his pocket blows up.
Below is a list of all the companies and products included in the 17 warning letters: Update: In response to receiving the FDA and FTC letters, every product on the list was removed from the market.
all 17 manufacturers, distributors and retailers that were warned by the agency in May, have stopped selling the nicotine-containing e-liquids used in e-cigarettes with labeling or advertising resembling kid-friendly food products, such as juice boxes, ca
The purpose of this notice is to provide information to organisations, businesses and members of the public concerned with tobacco and related products, regarding changes to the regulation of such products in the unlikely event that the UK leaves the Eur
The Tobacco Action Coalition of the Fingers Lakes partnered with Wayne County Public Health to hold a tenant meeting in the beginning stages of the process, providing information, listening to tenants’ concerns and answering questions.
“The Real Cost” has resulted in savings of more than $31 billion for youth, their families and society at large by reducing smoking-related costs like early loss of life, costly medical care, lost wages, lower productivity and increased disability – that
“We’re committing to provide additional information about the FDA’s science-based review decisions to manufacturers who’ve received a decision from the FDA that their product has not met the standards for authorization under the agency’s pathway for demon
Retailers that mix and prepare e-liquids or create or modify vaporizers may be regulated as both retailers and manufacturers. Importers of tobacco products must ensure that the tobacco products they import are in compliance with the law.
This guidance document is intended to assist any person who manufactures, packages, sells, offers to sell, distributes, or imports cigars or pipe tobacco with respect to the labeling requirements in sections 903(a)(2) and 920(a) of the Federal Food, Dr
This guidance represents the current thinking of the Food and Drug Administration (FDA or Agency) on this topic. It does not establish any rights for any person and is not binding on FDA or the public. You can use an alternative approach if it satisfies
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