Research & Policy Notes
Compounded semaglutide and tirzepatide are prepared by licensed pharmacies for individual patients but are not FDA‑approved products. Remedy’s safety pages note that the FDA has not evaluated these formulations for safety, quality, or efficacy.
On September 9, 2025, the U.S. Food and Drug Administration issued a warning letter to Remedy Meds alleging false or misleading claims about compounded GLP‑1s. While a warning letter is not a recall, it often requires changes to site content, labeling, or marketing.
Public reputation is mixed: Trustpilot shows strong satisfaction with responsive support, while the Better Business Bureau profile reflects a C‑ rating and complaint volume typical of high‑growth telehealth.
Operational guidance includes no additional shipping fees per help center materials, email tracking, and typical delivery within seven business days, with cold‑pack handling and no Friday–Sunday shipments for safety. Terms reserve the right to add shipping/handling fees.
- FDA warning letter to Remedy Meds (Sep 9, 2025)
- Compounded GLP‑1s are not FDA‑approved
- Labs included; typical delivery within 7 business days





