C-Qur Mesh Lawsuit
Since the entry of the C-Qur hernia mesh to the marketplace, there have been several reported instances of defects. Atrium first introduced C-Qur Mesh in 2005 through the 510(k) FDA approval system. This allowed medical devices to be introduced without rigorous premarket research and studies, which deemed controversial.
Financial compensation may be available for those who have experienced problems including infections, allergic reactions, abdominal pain, bowel adhesions, ulcers or organ perforation, mesh failure and/or revision surgery.
These issues are the responsibility of the medical device manufacturers and the parent companies. The parent companies ensure that their products are safe before advertising them to the public. Failure to do so is deemed negligent and grounds for litigation. Those who are injured as a result of a product defect may be eligible to receive personal injury compensation from any negligent parties.
Contact an experienced defective product lawyer to get additional information regarding your rights.