Lawyer Central is warning women who have been implanted with the Avaulta Solo, Avaulta Plus or Avaulta Biosynthetic of their risk for serious surgical mesh side effects. The Avaulta vaginal sling systems have been linked to a number of surgical mesh complications including infections, vaginal scarring and mesh erosions. If you or a loved one has suffered from Avaulta mesh complications, visit http://productliability.lawyercentral.com/Avaulta-Vaginal-Mesh-Complications--Defective-Medical-Device-Examples--10-41896-38.html and complete the Free Case Evaluation form to find out if you can recover compensation for the damages incurred as a result of your vaginal mesh side effects.
Women who have been implanted with an Avaulta vaginal mesh system may be at risk for erosion or extrusion of the mesh. This Avaulta mesh side effect may cause consistent pain and infection and may require the need for additional surgeries to remove the system. Other
Avaulta mesh complications can include the following: inflammation; pelvic pain; pain during sex; permanent nerve damage; vaginal and rectal problems; and scarring and deformation of the vaginal tissues. Problems with vaginal mesh systems were first brought to the public’s attention when the FDA released a warning in 2008 detailing the serious problems with transvaginal mesh systems. This
surgical mesh warning was issued after the FDA received more than 1000 reports of vaginal mesh complications from several companies, including C.R. Bard, manufacturer of the Avaulta systems.
Due to the serious side effects of the Avaulta mesh, recipients of the system may be able to file a
transvaginal mesh lawsuit for any resulting injuries. To find out if you can recover compensation for medical bills, pain and suffering and other damages related to your Avaulta mesh complications, visit LawyerCentral.com and complete the Free Case Evaluation form. The surgical mesh lawyers working with Lawyer Central are providing this online case review at no cost and are dedicated to defending the rights of patients who experienced problems with the Avaulta mesh or other defective medical devices.
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