Ethicon Hernia Mesh Lawsuits

Recalled hernia mesh causes pain, discomfort and the need for more surgeries

In May 2016, Johnson & Johnson recalled Ethicon Physiomesh Flexible Composite hernia mesh after studies showed the product had a higher rate of revision surgeries than other mesh products on the market.

Patients who received the product during open or laparoscopic surgery have reported the following complications:

  • daily pain
  • swelling
  • adhesions
  • obstructions
  • mesh migration
  • hernia recurrence
  • additional repair surgeries

If you or a loved one has suffered from complications due to hernia mesh that was implanted between 2010 and May 2016, it is important that you understand your legal rights. Our firm represents people nationwide who have been injured by defective hernia mesh products. Please contact us if we can be of assistance and read on for more important information about hernia mesh, hernia mesh lawsuits and your rights.

Start Your Free Case Review

    Give Us A Call


    Our Experienced Lawyers

    How can we help? Fill out the form for a free case review.

      Contact Us

      Case Types

      Related Posts