FREE CASE EVALUATION: 1-800-632-1404
If you are reading this page, you are likely suffering from pain after a prior surgery implanting a transvaginal mesh device / TVT / TVM system and sling.You may have been diagnosed with stress urinary incontinence or pelvic organ prolapse. Whatever the reason, you are likely in pain today, and we believe we can help you. If you would like to speak to a TVT lawyer, TVM lawyer or transvaginal mesh lawyer, please call us today for a free case evaluation.
A recent report reveals that complications from transvaginal mesh procedures are far from rare. Serious complications associated with the transvaginal placement of surgical mesh to repair pelvic organ prolapse (POP) are not rare, says the Food and Drug Administration in an updated safety warning to healthcare providers and patients. The most frequently reported complications (not associated with any particular brand of mesh) include mesh erosion through the vagina, pain, infection, bleeding, pain during sexual intercourse, organ perforation and urinary problems. The agency has also identified mesh contraction, or shrinkage, as a “previously unidentified risk” associated with transvaginal placement.
Surgical mesh is a medical device that is generally used to repair weakened or damaged tissue. It is made from porous absorbable or non-absorbable synthetic material or absorbable biologic material. In urogynecologic procedures, surgical mesh is permanently implanted to reinforce the weakened vaginal wall to repair pelvic organ prolapse or to support the urethra to treat urinary incontinence.
Pelvic organ prolapse (POP) occurs when the tissues that hold the pelvic organs in place become weak or stretched. Thirty to fifty percent of women may experience POP in their lifetime with 2 percent developing symptoms. When POP happens, the organs bulge (prolapse) into the vagina and sometimes prolapse past the vaginal opening. More than one pelvic organ can prolapse at the same time. Organs that can be involved in POP include the bladder, the uterus, the rectum, the top of the vagina (vaginal apex) after a hysterectomy, and the bowel.
BREAKING NEWS: Federal regulators are warning that women who receive vaginal mesh to treat pelvic organ prolapse face a serious risk of complications and health problems, and the devices appear to provide no benefits over other methods of treating the pelvic organ prolapse. The FDA issued a vaginal mesh safety communication on July 13, indicating that surgical mesh placed in the vagina to treat pelvic organ prolapse (POP) can erode through the vaginal tissue causing pain, infection, bleeding, pain during intercourse and urinary problems. There is also a risk of organ perforation during the surgical procedure to install a vaginal mesh, the agency stated. PLEASE READ THE FSA WARNING HERE.
The FDA first issued a warning about vaginal mesh complications in October 2008, indicating that, at that time, more than 1,000 people had reported experiencing problems with products made by at least nine different manufacturers. In addition, a study published earlier this year found a high risk of problems with all vaginal mesh implants.
The warning comes after a number of vaginal mesh lawsuits have been filed against several manufacturers by women who claim to have been injured by pelvic support systems. Our Firm represents women across the country who have received and been injured by TVM devices.
In our opinion, the FDA is already making clear statements that it is doubtful that the benefits of vaginal mesh implants outweigh the risks. FDA warned that transvaginal placement of surgical mesh carried the highest risk. There are other surgical techniques to address pelvic organ prolapse that do not involve the use of a surgical mesh or involve placement of the mesh in another part of the abdomen.
You may have experienced mesh erosion, bleeding, urinary infections, vaginal scarring, pain during sexual intercourse, failure to conduct sexual intercourse and more. A physician may have tried to remove the mesh and been unable to do so. You may be in excruciating pain, and need help. We are offering free case evaluations to the general public across the United States and Canada. Manufacturers we consider include American Medical Systems, Bard, Boston Scientific, Ethicon, Gynecare, and Johnson & Johnson.
If you received a transvaginal mesh / sling and have been injured, you may be entitled to monetary compensation. Problems include pain, inability to have intercourse, bleeding, mesh growth into the body, mesh erosion, and more. Problems could be irreversible. Please fill out the form to the right or call us so that we can provide you with forms to evaluate your potential case immediately.
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