Which procedure should drug distributors establish to manage recalls of RX drugs?

Establishing a procedure for handling recalls due to FDA or manufacturer actions is essential for drug distributors to ensure the safety and effectiveness of pharmaceuticals in the market. This procedure outlines the steps to take when a product needs to be removed from distribution due to safety concerns, quality defects, or labeling issues. By having such a procedure in place, distributors can swiftly communicate with retailers and healthcare providers, manage inventory effectively, and minimize potential harm to patients. This proactive approach not only adheres to regulatory requirements but also demonstrates the distributor's commitment to public health and safety.

Other options, while important, do not specifically address the critical element of managing recalls. Labeling drugs with expiry dates is a necessary practice for ensuring drug efficacy but does not directly deal with the process of recall management. Safe disposal of outdated drugs is crucial to avoid environmental contamination and ensure public safety but is not focused on how to handle the complexities involved in recalls. Lastly, auditing drug distributors annually is important for maintaining compliance and quality assurance, but it does not specifically relate to the recall procedure needed to respond to actions taken by regulatory agencies or manufacturers related to specific products.