How are recalls classified based on severity of risk?

Recalls are classified into three categories based on the severity of risk they pose to public health. Class I recalls involve situations where there is a reasonable probability that the use of, or exposure to, a product will cause serious adverse health consequences or death. Class II recalls pertain to products that may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote. Class III recalls involve products that are not likely to cause any adverse health consequences but that violate FDA labeling or manufacturing regulations.

Understanding this classification system is essential for ensuring proper communication about the risks associated with recalled products, facilitating appropriate responses from health professionals, and protecting consumer safety. The structured classification supports manufacturers and regulatory bodies in managing the recalls effectively based on the potential risk to the public.