PriceTracker GLP-1

What FDA’s record states

FDA record for the warning letter to Deluxe IV Aesthetics PLLC dba Deluxe IV and Aesthetics
FieldWhat FDA’s record statesSource
RecipientDeluxe IV Aesthetics PLLC dba Deluxe IV and AestheticsFDA letter
LocationLas Vegas, NVFDA letter
Letter dateFeb 20, 2026FDA letter
Posted by FDAMar 3, 2026FDA index
Issuing officeCenter for Drug Evaluation and Research (CDER)FDA letter
SubjectFalse & Misleading Claims/Misbranded (Telehealth)FDA letter
MARCS-CMS number721447FDA letter
GLP-1 drugs namedSemaglutide, TirzepatideFDA letter
Response letterNot published by FDAFDA letter
Closeout letterNot published by FDAFDA letter
“Las Vegas , NV 89179 United States admin@deluxeivaesthetics.com Issuing Office: Center for Drug Evaluation and Research (CDER) United States WARNING LETTER February 20, 2026 Deluxe IV and Aesthetics: This letter is to advise you that the United States Food and Drug Administration (FDA) reviewed your website content at the internet address https://deluxeivaesthetics.com, in December 2025, and has observed that your website offers compounded drug products, including semaglutide and tirzepatide drug products.”FDA warning letter to Deluxe IV Aesthetics PLLC dba Deluxe IV and Aesthetics, Feb 20, 2026 · read the full letter on fda.gov ↗

What this is and is not.A warning letter is FDA’s statement of what it considers significant violations. It is an allegation, not a court finding, and the firm can respond. A closeout letter is posted when FDA confirms the violations were corrected.

Other GLP-1 letters FDA issued that week

And 17 more in the full list.

Source

Every field above is copied from FDA’s page for this letter, read Oct 3, 2026. The letter on fda.gov ↗ · All 161 GLP-1 warning letters