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WARNING LETTER
•Vapor Rage LLC•October 26, 2021

Vapor Rage LLC – FDA Warning Letter, Oct 26, 2021

Record Details

The FDA issued a Warning Letter to Alexander Assa and Nick Mullen of Vapor Rage on October 15, 2021, following a review of their website, vapor-rage.com. The FDA determined that e-liquid products, specifically "Nancy’s Blend" and "Wicked Brew," were being manufactured and sold in the U.S. These products are classified as tobacco products under section 201(rr) of the FD&C Act and are subject to FDA jurisdiction.

The core violation is that these e-liquid products are "new tobacco products" as they were not commercially marketed in the U.S. as of February 15, 2007, and lack the required premarket authorization order under section 910(c)(1)(A)(i) of the FD&C Act. Consequently, these products are deemed adulterated under section 902(6)(A) and misbranded under section 903(a)(6) of the FD&C Act.

Vapor Rage is a registered manufacturer with over 1,800 products listed with the FDA. A Premarket Tobacco Product Application (PMTA) (STN PM0001115) submitted on September 5, 2020, resulted in a Refuse to Accept determination for 29 products on July 6, 2021, and a Marketing Denial Order

Company
Vapor Rage LLC
Inspection date
October 26, 2021
Product type
Tobacco
Office
Center for Tobacco Products
Person
  • Ann Simoneau (Director)
View Company Profile

ID · a4587b85-e39e-4825-9ed3-d890ca88cc44

Violation Codes10
21 U.S.C. 321(rr)21 U.S.C. 387a(b)21 CFR 1100.121 U.S.C. 387j(a)21 U.S.C. 387j(c)(1)(A)(i)21 U.S.C. 387e(j)21 U.S.C. 387e(j)(1)(A)(ii)21 U.S.C. 387e(j)(3)FD&C Act 902(6)(A)FD&C Act 903(a)(6)

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Other documents for Vapor Rage LLC
  • WARNING_LETTER - 2023-11-17November 17, 2023

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