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WARNING LETTER
•Trinity HealthCare Supply, LLC dba altRx•May 1, 2026

Trinity HealthCare Supply, LLC dba altRx – FDA Warning Letter, May 1, 2026

Record Details

In June 2026, the FDA issued a warning letter to Trinity HealthCare Supply, LLC, doing business as altRx, following an evaluation of the company’s website in May 2026. The review focused on the sale of compounded semaglutide and tirzepatide products used for weight loss. The FDA identified significant violations of the Federal Food, Drug, and Cosmetic Act, primarily involving the misbranding of these medications. Specifically, altRx displayed labels suggesting it was the manufacturer when it was not, and made claims that the products were "clinically proven." These statements misleadingly imply the drugs have undergone rigorous FDA approval or safety evaluations, which compounded medications do not receive. Under the regulatory framework of the FD&C Act, advertising and labeling must be truthful and not misleading. To achieve compliance, altRx must submit a written response within 15 business days outlining its corrective actions. This includes identifying the actual manufacturers of the products, providing accurate labeling samples, and removing all false or misleading claims from its website. The FDA warns that failure to rectify these issues promptly could lead to legal consequences such as product seizures or injunctions.

Company
Trinity HealthCare Supply, LLC dba altRx
Inspection date
May 1, 2026
Product type
drugs
Office
Center for Drug Evaluation and Research
Person
  • Matthew J. Lash (Acting Director)
View Company Profile

ID · 68d0ca2c-39a6-46f6-8167-0732d83545db

Violation Codes10
FD&C Act 502(a)FD&C Act 502(bb)21 U.S.C. 352(a)21 U.S.C. 352(bb)FD&C Act 301(a)21 U.S.C. 331FD&C Act 301(c)21 U.S.C. 331(c)FD&C Act 503AFD&C Act 503B

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