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Hernia Mesh Lawsuits

Hernia mesh is a surgical product used for hernia repair, chest wall reconstruction, and the treatment of traumatic or surgical wounds. A variety of products produced by major medical device manufacturers have been used in thousands of procedures across the United States. Now, certain models are facing increased scrutiny after a growing number of complaints from patients suffering serious complications and side effects.

If you or a loved one underwent hernia repair, wound treatment, or chest wall reconstruction and suffered infection, an allergic reaction, surgical mesh failure, or internal organ damage, you may be entitled to compensation. Crumley Roberts wants to help. Our attorneys have more than 25 years of experience helping injury victims, and we have the knowledge and resources to take on medical device companies. Call 866-336-4547 or complete our free online form to get help now.

Hernia Mesh May Put Patients at Risk of Complications

Injuries linked to certain models of hernia mesh include:

  • Infections
  • Allergic reactions
  • Mesh erosion or failure
  • Abdominal pain
  • Ulcers
  • Organ perforation
  • Bowel obstruction
  • Intestinal fistulas
  • Renal failure

If you or a loved one had a surgery involving the use of hernia mesh and suffered side effects, contact Crumley Roberts today.

Hernia Mesh Products Linked to Injuries

Surgeons use a variety of mesh products to repair hernias, but patient data indicates certain types of hernia mesh may pose an increased risk of injury to patients. These models include:

  • Atrium C-Qur™
    Production of Atrium’s coated C-Qur mesh was permanently halted on February 4, 2015, after the U.S. Food and Drug Administration (FDA) issued an injunction stopping the manufacture of the product at Atrium’s Hudson facility.
  • Bard Ventralex™ ST
    Ventralex ST, a plastic polyproprylene hernia mesh produced by C.R. Bard, Inc., has been linked to severe allergic reactions and side effects. Unlike transvaginal mesh, which is made of the same substance, there are no FDA warnings about use of Ventralex ST mesh for hernia repair.
  • Ethicon Physiomesh®
    Ethicon issued a voluntary recall of its Physiomesh hernia mesh after studies showed a higher than normal rate of hernia recurrence requiring surgery to correct.

Contact Our Hernia Mesh Lawyers

At Crumley Roberts, our attorneys are ready to help you get the compensation you deserve for your hernia mesh injury. We know you’ve suffered due to a medical device manufacturer’s negligence, and we want to hold the responsible parties accountable for the harm they’ve caused. Dial 866-336-4547 or complete our free initial consultation form to talk to a member of our 24/7 legal team.

C-Qur™ is a trademark of Atrium Medical Corporation and is used here only to identify the product in question. Ventralex™ is a registered trademark of C.R. Bard, Inc., and is used here only to identify the product in question. Physiomesh® is a registered trademark of Ethicon, Inc., and is used here only to identify the product in question.

This law firm is not associated with, sponsored by, or affiliated with Atrium Medical Corporation; C.R. Bard, Inc.; Ethicon, Inc.; or the U.S. Food and Drug Administration.

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