Complications with HERNIA MESH?

Experiencing complications due to a hernia mesh implant or procedure? Victims are starting to speak up and filing claims against their injuries. It’s time to do something for yourself or your loved one. You may be entitled to financial compensation. Get the Answers you deserve.


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Return of the Hernia

Implantable fabric meshes revolutionized hernia surgery and are being manufactured by multiple companies. Your surgeon can choose to repair a hernia by using hernia mesh surgery to bridge the opening without creating any tension. The benefits of hernia meshes come with some risks of complications. Hernia recurrence is the most common of hernia operations, including those in which mesh is used. The causes are improper surgical technique, shrinkage of the mesh, and movement or migration of the mesh. Second and subsequent hernia operations at the same site are more challenging and prone to failure than first attempts.


Are you suffering?

Did you know that each year, surgeons perform about one million hernia repairs? Surgeons consider Mesh Hernia the “gold standard” of care and when done properly, it is successful. Some of these surgeries are complicated with the following symptoms that can potentially lead to further surgeries. This is largely associated with recalled hernia mesh products that are no longer on the market.

  • Infections
  • Hernia recurrence
  • Autoimmune reactions
  • Migration in the body causing organ or tissue damage
  • Adhesions to the intestines
  • Fistulas
  • Bowel perforation
  • Documents that are coming to light conclude that patients of mesh hernia surgery have had to have a second or third surgery to remove the hernia mesh. Hernia Mesh lawsuits claim that manufacturers already knew of the potential risks AND never adequately warned patients or doctors of the potential problems. Some argue that companies were aware of problems and continued to make or sell faulty hernia mesh.

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    Cases are appearing…

    Mesh Hernia lawsuits accuse device makers of several counts of negligence, including:
  • Manufacturing a defective product
  • Failing to adequately test hernia mesh
  • Failing to warn the public about the risks of mesh
  • Intentionally, knowingly and recklessly concealing information about the defective mesh
  • Intentionally misrepresenting the quality and safety of hernia mesh
  • Negligently designing and marketing unsafe hernia mesh
  • In 2016, the FDA analyzed their reports that concerned Mesh Hernia complications and what the side effects were. The FDA found recalled surgical mesh has been responsible for some of the most serious hernia mesh complications. According to their website, “Many complications related to hernia repair with surgical mesh that have been reported to the FDA have been associated with recalled mesh products that are no longer on the market. Pain, infection, recurrence, adhesion, obstruction, and perforation are the most common complications associated with recalled mesh. In the FDA’s analysis of medical adverse event reports to the FDA, recalled mesh products were the main cause of bowel perforation and obstruction complications.” More and more people are speaking up and the awareness is spreading about the malpractices from some of these procedures and defective mesh hernia products. See some of the lawsuits that relate to hernia mesh.

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