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WARNING LETTER
•Vape4Less•May 1, 2024

Vape4Less – FDA Warning Letter, May 1, 2024

Record Details

On April 30, 2024, the FDA issued a Warning Letter to Bishoy Gerges of Vape4less.com, following a review of their website which revealed the sale and distribution of electronic nicotine delivery system (ENDS) products to U.S. customers. These products are classified as tobacco products under section 201(rr) of the FD&C Act, including those containing nicotine from any source, as amended by the Consolidated Appropriations Act, 2022.

The primary violation identified is the marketing of "new tobacco products" without the required premarket authorization order, as mandated by section 910(a) of the FD&C Act. Specifically, the products Lost Mary OS5000 – Cherry Banana Duo Ice, Funky Republic Ti7000 – Cantaloupe Apple, and Elf Bar – EB Design BC5000 – Watermelon Ice 13mL were cited. These products were not commercially marketed in the U.S. as of February 15, 2007, and lack FDA marketing authorization. Consequently, they are deemed adulterated under section 902(6)(A) and misbranded under section 903(a)(6) of the FD&C Act due to the absence of required notices or information.

Vape4less.com is required to submit a written response within 15 working days detailing actions taken to address

Company
Vape4Less
Inspection date
May 1, 2024
Product type
Tobacco
Office
Center for Tobacco Products
Person
  • Jill Atencio (Acting Director)
View Company Profile

ID · 5e3a2584-2f6a-440c-b3a1-4f728af117a0

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)21 U.S.C. 387b(6)(A)21 U.S.C. 387c(a)(6)

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