Ethicon Physiomesh™ is a large pore, flexible composite mesh made of non-absorbable polypropylene and used in minimally invasive ventral hernia repair and other fascial deficiencies. In May 2016, Ethicon removed many of their Physiomesh™ products from the market. Patients using the Ethicon Physiomesh™ are at a higher risk of revision surgeries and hernia recurrence based on an analysis of hernia repair reports. A direct cause of why the product is failing has not been determined according to Ethicon.

If you or someone you love suffered from complications due to Ethicon Physiomesh™, you may be entitled to compensation. Our law firm has years of experience helping patients harmed by defective medical devices, and we’re ready to help you too.


Physiomesh™ and Hernia Mesh Complications

According to the U.S. Food and Drug Administration (FDA), the most common adverse events reported for hernia repair surgery include:

  • Pain
  • Infection
  • Hernia recurrence
  • Adhesion
  • Intestinal blockage
  • Bleeding
  • Perforation (holes in organs or neighboring tissue)


Don’t Wait to Get the Help You Need

If you or someone you love suffered a hospital infection after surgery, you must act quickly to get the compensation you deserve. Contact our law firm today, and we’ll get started on your case immediately. There’s no cost or obligation, and you won’t pay us anything unless you recover compensation.

This law firm is not associated with, sponsored by, or affiliated with the FDA. Cases may be referred to associated law firms.

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