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(USGovernment-News.Com, February 25, 2014 ) New York, NY -- ClassAction.org is informing women who suffered complications following vaginal mesh surgery that they may still have time to file a claim. More than 30,000 lawsuits have been filed against makers of transvaginal mesh products alleging that the products are defective and dangerous. According to these lawsuits, the transvaginal mesh (TVM) implants can erode or shrink, causing women who have been implanted with the devices to suffer from pain, infection, bleeding and urinary problems. Manufacturers including C.R. Bard, Boston Scientific Corp and Ethicon are all defendants in a growing litigation that alleges these companies failed to adequately warn patients and physicians about the side effects associated with their products. If you were injured after being treated for pelvic organ prolapse (POP) or stress urinary incontinence (SUI) with a vaginal mesh implant, you may still have time to file a lawsuit against the product’s manufacturer. For more information, visit http://www.classaction.org/transvaginal-mesh-lawsuit.
In 2008, the FDA published a safety communication after reviewing more than 1,000 complaints of adverse events in women who received a transvaginal mesh (TVM) implant to treat pelvic organ prolapse (POP) or stress urinary incontinence (SUI). According to the agency, the most frequent complications with these implants included erosion of the mesh, infection, pain, urinary problems and recurrence of prolapse and/or incontinence. The FDA updated its safety communication three years later, after nearly 3,000 additional adverse event reports were submitted to the agency. In its update, the FDA announced that TVM implants have not been shown to provide any added benefits over traditional surgery without mesh. Furthermore, the agency said that “serious complications associated with surgical mesh for transvaginal repair of POP are not rare,” which was a change from what the agency previously reported.
Following the FDA’s warnings, thousands of lawsuits were filed alleging that TVM implants are defective and dangerous. According to the lawsuits, the mesh material can contract or shrink and cause inflammatory reactions in patients, with some side effects requiring surgical intervention. These lawsuits were recently consolidated to the Southern District of West Virginia in a procedure known as multidistrict litigation (MDL). This means that one judge, Judge Joseph R. Goodwin, will be overseeing all federally-filed lawsuits involving transvaginal mesh products made by several manufacturers. Although an MDL has been formed, women who were injured by vaginal mesh implants may still have time to file a lawsuit and seek compensation for their injuries.
Were you implanted with a transvaginal mesh device? If so, you may be eligible to collect compensation for past and future medical bills, pain and suffering and loss of marital relations. For more information, please click here.
About ClassAction.org
Class Action.org is dedicated to protecting consumers and investors in class actions and complex litigation throughout the United States. Class Action.org keeps consumers informed about product alerts, recalls, and emerging litigation and helps them take action against the manufacturers of defective products, drugs, and medical devices. Information about consumer fraud issues and environmental hazards is also available on the site. Visit ClassAction.org today for a no cost, no obligation case evaluation and information about your consumer rights.
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