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San Diego Product Liability Firm Provides Commentary on the Latest Developments in Transvaginal Mesh Litigation
Date:7/31/2014

he FDA and complications described in the scientific literature, the FDA identified surgical mesh for transvaginal repair of POP as an area of continuing serious concern,” the FDA said in the 2011 update. “The FDA is issuing this update to inform you that serious complications associated with surgical mesh for transvaginal repair of POP are not rare.”*

According to the FDA’s safety communication, the agency received more than 1,000 reports of adverse events involving transvaginal mesh from 2005 to 2007 and another 2,874 reports of complications from Jan. 1, 2008 to Dec.31, 2010. The most commonly reported problems, according to the FDA, include mesh erosion, organ perforation, pain, infection, bleeding and urinary problems.

“Even though the FDA recognized possible problems with transvaginal mesh products, they continue to be used,” said Helbock. “We are keeping a close watch on the litigation and are happy with the Endo settlement.”

For more information or to speak with a San Diego personal injury lawyer about a possible transvaginal mesh claim, contact The Law Office of Melinda J. Helbock, A.P.C.

Sources:
*http://www.fda.gov/MedicalDevices/Safety/AlertsandNotices/ucm262435.htm

Read the full story at http://www.prweb.com/releases/transvaginal-mesh/case-reviews/prweb12046969.htm.


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