Transvaginal Mesh Injury Lawyers in Frisco, Texas

The new media is focusing on reporting on events concerning recent lawsuits filed on behalf of women who have undergone the transvaginal mesh procedures. One woman after another is coming forward with stories about how they’ve suffered since having the transvaginal mesh procedure performed.

Ethicon, a subsidiary of Johnson & Johnson, along with Boston Scientific have been named in these suits, but there are almost 30 companies that have sold the device.  It was first touted as a solution for those with pelvic organ prolapse (POP) and incontinence due to weakened pelvic and vaginal walls. Though it was designed to support this tissue, it has had many problems, such as mesh erosion through the vagina and bowel.  Victims may need to have numerous corrective surgeries.

This procedure was designed to be a permanent solution, so doctors have had very little success in removing transvaginal mesh. The current lawsuits illuminate some startling facts. Victims believe that the companies who manufacture these products failed to perform the required FDA testing and that they failed to warn the public about the dangers. In one case filed against Ethicon, the company was ordered to pay a little over $3 million in damages.

Many speculate that a number of victims have not come forward because of the sensitive nature of this issue and its ongoing intimate implications. If you or someone you know has had this surgery and are experiencing complications, then you should seek the advice of a skilled and informed Frisco attorney.

To date, thousands of transvaginal mesh lawsuits have been filed, but there are still victims out there who are reluctant to come forward in spite of their pain and suffering. Many experts believe that the manufacturers of the transvaginal mesh skirted the U.S. FDA’s guidelines using loopholes in the system. Some allege that these companies are more interested in seeing who can get their product to the market first instead of the safety of consumers.

Victims are understandably upset and searching for answers. Though the FDA has now ordered over 30 of these manufacturers to perform post-market safety tests, it is simply too late for those who have already undergone the procedure. These victims may never be able to be totally free of all pain and suffering and enjoy a healthy quality of life again.