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FDA Rejects Bidi Vapor's Bidi Stick Classic Market Application, Again

Regulations by 2FIRSTS.ai
Jan.23.2024
FDA Rejects Bidi Vapor's Bidi Stick Classic Market Application, Again
US FDA rejects Bidi Vapor LLC's application for marketing Bidi Stick Classic e-cigarette, prohibiting its sale or distribution in the US.

According to a report by journalnow on January 22, the US Food and Drug Administration (FDA) has rejected Bidi Vapor LLC's market application for the Bidi Stick Classic e-cigarette.

 

After the FDA issued a marketing denial order, Bidi vapour company has been prohibited from selling or distributing its product in the US market, otherwise it will face enforcement actions from the FDA. However, Bidi vapour company has the right to submit a new marketing application to the FDA.

 

According to the FDA's requirements, e-cigarette manufacturers must prove that their products not only serve as a reduced-risk alternative for adult smokers but also ensure that the transition to their products does not result in the illegal use of these products by individuals under the age of 21. However, the FDA believes that Bidi Vapor Company has failed to meet these evidentiary requirements.

 

References:
[1] FDA denies Bidi Vapor application for marketing approval
Also Read:
[1] Bidi Proposes Scan Data to Identify Non-compliant E-cigarette Companies
[2] FDA Issues MDO for Suorin and blu PLUS+ E-cigarettes
[3] VTA: FDA CTP's Actions Undermine Public Health
[4] US Senator Pushes FDA to Protect Children from E-cigarette Harm
[5] Appeal Filed Against FDA's Marketing Denial Order on SMOK Products
[6] FDA Issues Marketing Denial Order for 22 SMOK E-cigarette Products
#North America#United States#Legislation#Open system e-cigarettes#FDA#E-cigarette Market

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