What is one of the purposes of drug recalls?

One of the primary purposes of drug recalls is to remove misbranded or adulterated products from the market. When a drug is determined to be unsafe, ineffective, or not manufactured according to regulatory standards, a recall is initiated to protect public health. This action ensures that consumers do not have access to drugs that may pose a risk due to contamination, labeling errors, or other safety concerns.

In this context, misbranding refers to products with misleading or false labeling that may deceive consumers, while adulteration involves drugs that have been contaminated or do not meet quality standards. By conducting recalls, regulatory agencies, such as the FDA, act to safeguard patients by ensuring that only safe and effective medications are available in the marketplace. This is an essential function of public health and safety oversight in the pharmaceutical industry, demonstrating a commitment to consumer protection.

The other options do not align with the fundamental objectives of drug recalls, which focus solely on the safety and effectiveness of medications rather than marketing strategies or production increases.