An endotoxin is a toxic component of the outer cell wall of certain bacteria, released when the bacteria break down. When it contaminates an injectable product, it can cause fever, chills, low blood pressure, and other serious reactions, even if the product no longer contains live bacteria.
Controlling endotoxin levels is a routine part of regulated sterile drug manufacturing. It is a documented risk with unregulated or grey-market peptides and injectables made without that oversight: when researchers test-bought semaglutide from illegal online pharmacies, endotoxin turned up in all three vials that arrived (Ashraf et al., Journal of Medical Internet Research, 2024 (external link)). That is one reason the source and quality controls of an injected product matter. See research peptides and GLP-1 medications.