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Multiple Vaginal Mesh Lawsuits Filed Against Ethicon, Inc. on Behalf of Women Seriously Injured Allegedly Due to Vaginal Mesh Sling Defects, Reports Wright & Schulte
Date:4/26/2013

lic About Serious Vaginal Mesh Complications
The FDA issued a vaginal mesh injuries warning in 2011, alerting the public that transvaginal mesh complications are more common than manufacturers had previously disclosed and that, in some cases, implantation of vaginal mesh devices was no more effective than traditional surgeries. Specifically, after reviewing more than 100 bladder mesh sling studies, the FDA found that about 10 percent women with these devices have developed or would develop serious injuries that require revision surgery and possibly vaginal mesh removal within one year of implantation. In some of the worst cases, women reportedly needed multiple revision surgeries to repair the damage caused by bladder mesh slings.

Other significant points included in the 2011 FDA public warning were that vaginal mesh devices had greater risks of complications than traditional surgery for treating POP and SUI and that vaginal mesh may not even be sufficient at alleviating the symptoms of prolapse. [fda.gov/downloads/MedicalDevices/Safety/AlertsandNotices/UCM262760.pdf]

About Wright & Schulte LLC
Wright & Schulte LLC, an experienced personal injury firm, is dedicated to the belief that America’s legal system should work for the people. Every day, the attorneys of Wright & Schulte LLC stand up for the rights of people who have been injured or wronged and fight tirelessly to ensure that even the world’s most powerful corporations take responsibility for their actions. If you’re looking for a law firm that will guarantee the aggressive and personal representation you deserve, please do not hesitate to contact Wright & Schulte LLC today. Free case evaluations are available through yourlegalhelp.com or by calling 1-800-399-0795.

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Wright & Schulte LLC
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1-800-399-0795

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