What is Transvaginal Mesh? Transvaginal mesh is a type of medical implant that is used to treat conditions like pelvic organ prolapse (POP) and stress urinary incontinence (SUI). The mesh is implanted through the vagina and is used to support structures such as the bladder, urethra, uterus, rectum, vagina, or small bowel. What Problems Are…
Vaginal Mesh Lawsuit Guidelines
Doctors use transvaginal mesh to treat medical conditions like stress urinary incontinence, or SUI, and pelvic organ prolapse or POP. The mesh’s original use was to repair hernias, but during the 1970s, surgeons began using the product to support vaginal tissue. In 1996, the Federal Drug Administration, or FDA, officially approved its use for SUI. Later, in 2002, vaginal mesh was authorized for POP. Unfortunately, women started suffering from complications after the surgery. Women who are having postsurgical trouble from the product may consider filing a vaginal mesh lawsuit since manufacturers of the surgical material did not warn surgeons or patients about the risks. Women who file a lawsuit may obtain compensation for medical expenses, pain and suffering.
Surgery Details and Potential Complications
Surgeons can perform a POP surgery through a woman’s vagina or abdomen. The procedure involves the use of stitches or surgical mesh to reinforce the patient’s pelvic organs. After people began reporting problems, the FDA investigated and issued a statement confirming that women who select a surgical mesh treatment may face a higher risk of developing complications than they would if they chose another type of treatment. The agency also asserts that the product does not offer advantages to other treatment options. If a woman begins to experience medical problems after a mesh procedure, then she should consider filing a vaginal mesh lawsuit.
Mesh manufacturers form the surgical product from animal tissue, non-absorbable polypropylene, absorbable synthetic materials or polyester. Some producers make the product from a combination of the materials. Women who have filed a vaginal mesh lawsuit typically have the polypropylene or polyester mesh product as they are the most common materials used by the medical community. According to research, an estimated 50 percent of women will face POP, but only a few of them will need surgery to treat the problem. About 24 percent of women suffer from SUI, and surgery is just one way to treat the ailment.
Common vaginal mesh complications include bleeding, mesh erosion, urinary troubles and infection along with pain during intercourse, scarring and tearing in the bladder, bowel or blood vessels. Research confirms that as of 2011, more than 4,000 adverse events have occurred from the surgical product. The most frequent complication was mesh erosion. A study involving 12,000 patients verified that about 10 percent of them experienced erosion within one year of the procedure. Some patients reported problems within a month, but the average erosion timeframe was 4.1 months for women who had the vaginal procedure. The average erosion timeframe for women who opted for the abdominal surgery was 15.6 months. Vaginal mesh lawsuits have been filed to help people deal with the painful problems associated with the surgical treatment option.
FDA Involvement and Vaginal Mesh Brands that Frequently Fail
During July 2011, the FDA released a warning about transvaginal mesh products. Specifically, the agency advised people to review other options when applicable medical conditions arise. Furthermore, the FDA intends to review the product in detail to determine whether surgeons should continue using it.
The FDA also released a list of brands that have been causing problems for women. The list includes brands like American Medical Systems, C.R. Bard and Boston Scientific as well as Ethicon, Inc., which is a division of Johnson & Johnson.
Due to the recent FDA warnings, women who are suffering from complications after a mesh procedure may consider filing a vaginal mesh lawsuit or joining an ongoing one. In most cases, there is a time limit to file a mesh lawsuit, so be sure to contact us right away for legal help.
Know your legal rights. Contact a lawyer about filing an Ethicon Gynecare transvaginal mesh lawsuit. Our lawyers are currently meeting with women that have experienced a vaginal mesh complication. We offer compassion and confidentiality as well as no legal fees to pay unless you win your case. Women across the country have already been rewarded with millions of dollars for their suffering through individual Ethicon Gynecare vaginal mesh lawsuits and class action lawsuits are also being filed at this time as well. Please contact our 24 hour hotline at 1-800-732-3070 or fill in a form on the side of this page.
Further Vaginal Mesh Lawsuit Info
Ethicon Gynecare is one of the leading companies that manufacturer surgical mesh devices used to treat pelvic organ prolapse in women. However, these products are currently under legal scrutiny for the irreversible damage that they can cause. Lawyers across the country are currently meeting with women that have experienced a vaginal mesh complication to discuss…
America Medical Systems is one of the leading manufacturers of surgical mesh and vaginal mesh products that are under legal scrutiny for the complications they can cause women. Lawyers are currently meeting with women that have suffered vaginal mesh complications to discuss their legal rights to file an American Medical Systems surgical mesh lawsuit. Surgical…
Vaginal mesh products, including the Coloplast Vaginal Mesh and Bladder Sling are designed to provide relief from urinary continence and pelvic organ prolapse. When the pelvic floor muscles begin to fail this can result in the pelvic organs protruding out of the body and the ability to hold in urine can become impossible. This is…
There are several different companies that are under investigation and that could be faced with a vaginal mesh lawsuit after failing to warn patients about the side effects of their product including Boston Scientific. Boston Scientific is a trusted name in the medical industry and thus many doctors and patients believed that they were telling…