What is indicated by a product being classified as 'adulterated'?

A product classified as 'adulterated' signifies that it has been manufactured under unsanitary conditions, which compromises its quality and safety. The term implies that the product may contain harmful or unapproved substances that can pose health risks to consumers.

In the context of pharmaceuticals, adherence to strict guidelines regarding manufacturing conditions is critical to ensure that products are safe for patient use. Adulteration can occur during various stages, including the sourcing of raw materials, production processes, and storage. Identifying a product as adulterated raises significant concerns regarding its integrity and the potential risks to health, leading to regulatory actions to address those issues.

Other classifications, such as false labeling or being FDA approved, relate more to misrepresentation and compliance rather than the actual manufacturing conditions impacting product safety and efficacy.