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In September 2025, the FDA reported instances of compounded GLP-1 products containing unapproved foreign substances and companies selling drugs to consumers that were falsely labeled for research purposes. A 2024 report also found that many active pharmaceutical ingredients for compounded GLP-1s were imported from unregistered foreign suppliers, raising questions about supply chain oversight
4,5 Given the popularity of semaglutides and related drugs, Emergency Medical Services (EMS) need to be aware of the potential emergencies that may be encountered
15, 2025) as a domestic inspection since the Genzyme facility is located in New York State, not in France
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