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Bladder Mesh Sling Lawsuit Filed by Wright & Schulte on Behalf of an Iowa Woman Who Sustained Serious Injuries Allegedly Due to Defective Vaginal Mesh Implants
Date:5/1/2013

nd medical devices. Our skilled vaginal mesh attorneys are experienced at successfully going up against large corporations. We encourage those who believe they have been injured due to use of Ethicon’s or any company's vaginal slings to speak with our knowledgeable transvaginal mesh lawsuit lawyers 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 Gynecare Gynemesh™ PS with Non-absorbable Prolene™ Soft Mesh and transvaginal tape (TVT) [ethicon360emea.com/products/gynecare-gynemesh-ps] implanted in January 2008 to treat her pelvic organ prolapse (POP) and her stress urinary incontinence (SUI). After having this bladder mesh sling implanted, however, the plaintiff developed severely painful complications that allegedly impaired her quality of life by causing her to sustain permanent injuries.

Among the serious complications and injuries reportedly associated with the Gynecare Gynemesh™ PS and TVT 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. [fda.gov/downloads/MedicalDevices/Safety/AlertsandNotices/UCM262760.pdf]

FDA Warning Concerning Vaginal Mesh Risks
In 2011, the Food and Drug Administration (FDA) issued an alarming warning that transvaginal mesh complications more common than manufacturers had disclosed to the public and that, in some cases, implantation of vaginal mesh devices was no more effective than traditional surgeries.

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