Vaginal Mesh Complications

Vaginal Mesh Complications prompt multiple FDA warnings.

Between 2008 to 2010, the FDA collected more than 2,800 reports of vaginal mesh complications. This prompted an FDA warning in 2011 regarding the high incidence of complications associated with vaginal mesh when used to treat Pelvic Organ Prolapse.

Transvaginal mesh is a surgical mesh used to treat medical conditions including pelvic organ prolapse (“POP”) and stress urinary incontinence (“SUI”). Initially, this surgical material was used in hernia repair procedures. In the 1970s, gynecological surgeons began using it to reinforce the tissues in the vagina during a POP repair procedure. The FDA approved the use of the mesh for SUI in 1996 and for POP in 2002. However, there are now reports of vaginal mesh complications and vaginal mesh lawyers are coming forward to help affected parties pursue legal action against manufacturers of these products.

What Are Vaginal Mesh Complications?

This mesh generally comes in four types of materials: animal tissue, absorbable synthetics, non-absorbable polypropylene or polyester, and a combination of these. Polypropylene or polyester are most commonly used in female urology and gynecological surgeries. While as many as 50 percent of women may experience POP, only a small percentage require surgery. Approximately 24 percent of women experience SUI and surgery is one treatment for the condition.

As of 2011, there have been more than 4,000 adverse event reports regarding the mesh used in these surgeries. With POP repair, complications included infections in the mesh area, urinary tract issues, pain, mesh site bleeding, and local organ damage. The most common complication was erosion of the mesh. In one of the largest studies, which involved 12,000 women, approximately ten percent of women who had the mesh inserted experienced mesh erosion within only one year following their surgeries.

Size of the mesh implant, low levels of estrogen, advanced age, and certain surgical techniques were also shown to increase risk. Most problems became apparent after a month or more following surgery. Erosion timeframe varied by surgery, with an average of 4.1 months for vaginal incision and 15.6 months for an abdominal incision. As these complications were revealed, transvaginal mesh lawyers came forward to help patients deal with the situation.

Brands Causing Vaginal Mesh Complications

The U.S. Food and Drug Administration published a safety warning regarding transvaginal mesh in July 2011. The agency recommended that patients and doctors consider alternative treatments for relevant medical conditions. It also revealed plans to establish an advisory panel that would determine whether this mesh should be taken off the market. Extensive safety testing was recommended and this was later supported by the Obstetrics and Gynecology Devices Advisory Panel.

The FDA advisory included multiple vaginal mesh brands and models of this vaginal mesh. Transvaginal mesh lawyers subsequently released their own lists of mesh products that could potentially cause severe complications. On these lists were major brands like American Medical Systems, Boston Scientific, Coloplast, C.R. Bard, and Ethicon, Inc., which is a Johnson & Johnson company.

Since transvaginal mesh lawyers have a complete understanding of the issues involved, they are able to provide assistance from a legal standpoint and have made many patients feel more secure. Those who received this mesh as treatment for medical conditions, like SUI and POP, know that they have legal recourse should they experience complications. With professional legal guidance at their disposal, going down this road will be less complicated if such action becomes necessary.

Victims of Vaginal Mesh Complications Should Consult Their Doctor

If you or a loved one suffered mesh complications following transvaginal mesh surgery, it is important that you consult your doctor immediately and seek legal counsel. Be sure to keep records of your medical appointments, procedures, and expenses, as your transvaginal mesh lawyer will need this information should you choose to seek compensation for your injuries.

If you would like additional information regarding your avenues for legal recourse, we urge you to contact Bernstein Liebhard LLP as soon as possible. Our experienced transvaginal mesh lawyers will thoroughly evaluate your case, and file an individual lawsuit on your behalf if you have a valid claim. To speak with one of our transvaginal mesh lawyers, please call 1-(888)-217-3033 or fill out our Free Case Evaluation form, and someone from our legal staff will contact you immediately.

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