Transvaginal mesh or vaginal mesh and bladder slings have caused serious medical complications for hundreds of women who suffer from vaginal prolapse, also known as pelvic organ prolapse. Transvaginal mesh patches used in the procedures are manufactured by Bard, Tyco, Mentor, Johnson & Johnson(Ethicon), AMS and Boston Scientific. Symptoms range from infections, bleeding, urine leakage, pain and bladder obstruction. If you have a transvaginal mesh patch or bladder sling and feel that you may have one of these complications, please feel free to contact us immediately by clicking on the phone to the right, entering your number in the space provided and clicking again; your phone will usually ring within one minute. You may be eligible to be a part of the vaginal mesh lawsuit
Since 2008, the FDA has received 2874 adverse event reports of complications following surgery. Of the 2974 reports, 1503 adverse event reports were associated with transvaginal implants used in Pelvic Organ Prolapse repair, and 1371 of the reports were associated with stress urinary incontinence repair. TransVaginal mesh was designed to help women who were suffering from Pelvic Organ Prolapse and Stress Urinary Incontinence, but instead it has shown to cause serious complications which have resulted in the vaginal mesh lawsuit. Studies have shown that due to the nature of this surgery, surgeons placing Transvaginal mesh devices need more specialized training on using and implanting the device. Since there are serious complications and infections that can arise during the surgery and implantation of the device, transvaginal mesh can do more harm than good for many women. Due to the complications of vaginal mesh surgery the transvaginal mesh lawsuit is proceeding forward to assist those women who have been injured from the use of vaginal mesh.