The U.S. Food and Drug Administration (FDA) has the job of preserving the public health of all U.S. consumers through the regulation of a myriad of potential health risks; this includes human and veterinary drugs, biological products, medical devices, food, cosmetics, and products that emit radiation.
While the FDA’s mission is to protect consumers, many previously-approved items have resulted in recalls, long-term injuries, and lawsuits, calling into question the efficacy of their approval process.
Drugs alone have averaged 1,284 recalls per year since 2012. The continued frequency of FDA recalls has sparked both skepticism and scrutiny from the public. This comprehensive study will take a more granular look at FDA recall process since 2012 up until now.
We cover which firms experience the most recalls, how the FDA’s adverse events reporting system relates to drug recalls, and how you as a consumer can report injuries from the medical treatment you’ve been given.
Link to FDA Study