Hernia Mesh

Individuals who have had revision surgery related to hernia mesh or repair and suffer from complications related to surgical mesh may be able to take action against the manufacturers of the products used. There have been recalls of certain types of hernia mesh in the last few years, including different models of Kugel mesh, manufactured by C.R. Bard. Additionally, in 2016, the Physiomesh device was taken off the market by the manufacturer, Ethicon.

The attorneys of Goldenberg Heller & Antognoli have more than 30 years of legal experience and our team is prepared to help our clients hold responsible parties accountable for the pain and discomfort they have caused.

Our Approach to Hernia Mesh Claims

Many different brands of hernia mesh have caused problems that lead to revisions of the mesh that we are investigating. Those products include:

  • Physiomesh
  • Ethicon Proceed
  • C-Qur/Atrium
  • Bard Kugel Mesh & Hernia Patch

These hernia mesh models have been linked to serious side effects, including allergic reactions, mesh erosion or failure, bowel obstruction, ulcers, organ perforation and more. Symptoms include constipation, fatigue, fever, irritable bowel, severe pain and urinary issues. If you or a loved one experiences any of these symptoms, contact your treating physician immediately.

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Free Hernia Mesh Claims Consultation

We assist Hernia Mesh clients in Illinois, Missouri and across the country. We are ready to discuss your specific legal needs and help you get the compensation you deserve.

“Your knowledge, patience, and comfortable approach made this experience much easier for me.”

-T.C.

“Your firm is so professional. They make me feel like family more than anything else. Everyone is very kind and courteous. They go to no limits to get the job done.”

-A.S.

“I get answers to all my questions the day I call, that alone is wonderful. I am very happy to have Goldenberg Heller & Antognoli representing me.”

-D.J.

2017

Notable Settlements & Verdicts

Obtained over $1 million in settlements for individuals injured by a pharmaceutical drug that increased the risk of cancer.

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about your case.

800.782.8492

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