
According to the Food and Drug Administration (FDA), “A drug recall is the most effective way to protect the public from a defective or potentially harmful product. A recall is a voluntary action taken by a company at any time to remove a defective drug product from the market.”
The FDA has three classes of recalls:
- Class I: A dangerous or defective product that could cause serious health problems or death.
- Class II: A dangerous product that might cause temporary health problems or pose a slight threat of a serious nature.
- Class III: A product that is unlikely to cause any adverse health reaction but that violates FDA labeling or manufactures laws.
If you or a loved one has been harmed due to a defective prescription drug, please seek legal assistance from Elmiron attorneys at Colson Hicks Eidson.








