Which classification is given to products that are incorrectly labeled?

The classification given to products that are incorrectly labeled is "misbranded." This term specifically refers to situations where the labeling of a product is misleading, incorrect, or fails to provide required information as mandated by regulatory agencies, particularly the Food and Drug Administration (FDA) in the United States. Misbranding can include a variety of labeling issues, such as false or misleading statements about the product, failure to include necessary warnings, or not disclosing essential information that consumers need to make informed decisions.

In the context of regulatory affairs, identifying a product as misbranded is significant because it implies that the product does not meet the legal requirements for labeling, potentially leading to consumer harm or confusion. This classification is crucial in maintaining public health and safety, as well as ensuring that consumers receive accurate and truthful information about the products they use.

Other classifications such as non-compliant, adverse, and defective do pertain to regulatory concerns but are used in different contexts. Non-compliance refers more broadly to not adhering to regulations, adverse is often associated with negative effects or reactions stemming from a product, and defective pertains to physical flaws or flaws in design or manufacturing, rather than labeling issues. Thus, "misbranded" is the precise term for incorrectly labeled products.