Johnson & Johnson Mesh Slings Cause Erosion, Pain, Incontinence

July 13th, 2016

transvaginal mesh

Hundreds of lawsuits have been filed against Johnson & Johnson due to complications caused by their transvaginal mesh slings. The mesh slings, or Mentor ObTape sling, is used to treat stress urinary incontinence (SUI) and pelvic organ prolapse (POP) in women. This mesh was originally used to treat hernia repairs in the 1950’s. In the 1970’s doctors began using the mesh abdominally to treat SUI and POP. Physicians cut a piece of mesh into the desired shape and surgically implanted it in the abdomen.

The Food and Drug Administration did not approve the use of transvaginal mesh until the year 1996. The FDA did not require studies of the drug on humans before they approved it. These transvaginal mesh slings have been found to cause major complications in women. The mesh can erode through the tissue of the vagina and cause bleeding and painful intercourse. In some cases, the erosion goes into the bowel and can lead to infection. Some women experience incontinence, pain, and discharge. Often women undergo revision surgeries only to discover that the mesh has become absorbed into the tissue of the vagina and cannot be easily removed.

Physicians and consumers were not warned of these possible complications until it was too late for many women. Pharmaceutical manufacturer Johnson & Johnson has agreed to settle over 100 lawsuits regarding their mesh sling product, awarding some women over a million dollars.

What you can do

If you or someone you know has used mesh slings and suffered any of the above injuries contact us today. We will evaluate your case to determine if transvaginal mesh is to blame for your complications. These types of injuries can take a heavy toll on people both physically and financially. We know how difficult this can be for you and your family. Contact the Garmon Law Firm today to get the compensation you deserve.

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