Every year, 1 million procedures in the US involve the use of hernia mesh to support the tissue that has been injured. The mesh is applied over the region containing the hernia and secured by the surgeon with sutures, staples, or adhesive. Tissue can grow inside the device because to pores in the mesh.
The U.S. Food and Drug Administration claims that employing hernia mesh may enhance a patient’s prognosis since the procedure and recuperation time may be quicker than with other types of therapy. However, the organisation attributes several instances of hernia mesh problems to recalled meshes.
Have you had any health issues since having surgery for an abdominal hernia? Have you had a further operation to treat a reoccurring hernia?
Adhesion, intestinal blockage or perforation, infection, rejection, and migration are all risks associated with hernia mesh. Patients who had hernia mesh implants have reported hernia recurrence and persistent discomfort as signs of mesh failure. The FDA deems the mesh used to treat hernias to be safe, but problems can occasionally happen.
According to one research, complications from hernia surgery affect over one-third of patients, with severe discomfort being the most common complaint.
The American Food and Drug Administration keeps note of any reported hernia mesh issues. According to the FDA, the intestinal perforation and blockage that occurred in those patients was “primarily caused” by the recalled mesh. Some of the worst side effects of hernia mesh include bowel perforation and blockage.
COMPLICATIONS WITH HERNIA MESH INCLUDE:
- Adhesion
- Intestine Blockage
- A Perforated Bowel
- Infection Rejection
- Migration Recurrence
- Continual Pain
You could be entitled to money damages if Mesh caused harm to you or someone you care about. It’s possible that a lawsuit may develop with significant financial settlements from claims.
