Record status
Active safety communication
- Agency
- U.S. Food and Drug Administration
- Action
- Compounding risk alert
- Stage
- Safety communication
- Last verified
- Jul 10, 2026
FDA · Safety alert
FDA reported adverse events, including some requiring hospitalization, associated with dosing errors involving compounded injectable semaglutide and described risks tied to varying concentrations, vial-and-syringe measurement, and unit conversion.
Record status
Editorial boundary: Peptide Report summarizes the public source and preserves its procedural stage. This page does not convert an allegation, proposal, advisory discussion, or warning into a final legal conclusion.