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TransVaginal Mesh Lawsuit Filed on Behalf of a Georgia Woman Seriously Injured Allegedly Due to Defective TransVaginal Mesh Implants, Reports Wright & Schulte
Date:4/4/2013

s-mount-as-wright-schulte-llc-files-new-vaginal-mesh-lawsuit-in-american-medical-systems-litigation/1363" title="transvaginal-mesh-lawsuits-mount-as-wright-schulte-llc-files-new-vaginal-mesh-lawsuit-in-american-medical-systems-litigation/1363" onclick="linkClick(this.href)">transvaginal mesh lawsuit attorneys by visiting yourlegalhelp.com or by calling 1-800-399-0795.

Serious Vaginal Mesh Injuries
The complaint explains that the plaintiff underwent surgery to have the Lynx™ Suprapubic Mid-Urethral Sling System featuring Advantage™ Mesh implanted in December 2007 to treat her pelvic organ prolapse (POP) and her stress urinary incontinence (SUI). However, following implantation, the plaintiff developed severely painful complications that allegedly impaired her quality of life by causing permanent injuries. [http://www.bostonscientific.com/templatedata/imports
/collateral/Gynecology/broc_Lynx_01_ug_us.pdf]

Some of the severe injuries reportedly associated with the Lynx™ Suprapubic Mid-Urethral Sling System are pelvic and urinary pain, dyspareunia (pain during sexual intercourse), vaginal scaring, mesh erosion through the vaginal lining, an increased risk of infection, puncturing of the blood vessels/bowels/bladder and recurrence of SUI.
[http://www.fda.gov/downloads/MedicalDevices/Safety/AlertsandNotices/UCM262760.pdf

FDA Warning Concerning Vaginal Mesh Risks
After reviewing more than 100 studies focused on bladder mesh devices, in 2011, the Food and Drug Administration (FDA) released a public warning announcing that transvaginal mesh complications more common than manufacturers had let on and that, in some cases, implantation of vaginal mesh devices was no more effective than traditional
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