Vaginal Mesh Lawsuits Updates, New News From Vaginal Mesh Lawyers

Vaginal Mesh Helpline is keeping women informed with a mesh update on the all the new  vaginal mesh lawsuits. All vaginal mesh lawyers suggest filing your mesh lawsuit  right away. We do not want any women to be left out.

A 47-year-old former nurse, Gross testified that Ethicon’s Prolift vaginal mesh implant has rendered her unable to work, have sex with her husband, or sit comfortably for more than 20 minutes. (Gross v. Gynecare Inc., Atl-L-6966-10, Superior Court of Atlantic County, New Jersey.) Gross also said that, as a result of the Prolift mesh, she takes up to 20 medications a day and has undergone more than 400 medical encounters, including physical therapy sessions, doctor visits, and many surgeries.

The Charleston woman claims that she suffered serious complications after AMS surgery, when she was implanted with the Elevate transvaginal mesh back in January 2011. The lawsuit alleges that she suffered substantial physical pain and suffering, emotional distress, and economic loss due to medical expenses. These damages, according to the suit, were the direct result of the AMS transvaginal mesh manufacturer’s negligent and wrongful actions. Further, the defendants, AMS, allegedly knew about the risks involved with its transvaginal mesh product but failed to warn the plaintiff.

A Georgia women’s  doctor suggested the mesh when she mentioned that she had bladder leakage when she laughed or coughed. Shortly after the surgery, it felt like razors were slicing her organs and a sharp edge of the mesh cut her boyfriend during sex, she said. Even though she eventually had it removed, the 55-year-old west Georgia woman still has pain she believes is caused by the mesh.

According to court documents, on January 7th, 2013 a Minnesota woman filed a lawsuit in Minnesota District Court (case no. 0:2013cv00060) alleging she suffered serious complications from her Transvaginal Mesh. Transvaginal surgical mesh is used to treat pelvic organ prolapse (POP) and Stress Urinary Incontinence (SUI). Defendant is Boston Scientific and in the lawsuit, plaintiff claims that after surgical implantation with defendant’s Lynx sling she suffered complications.

Vaginal mesh Bell Weather Case Updates

The  first bellwether trials in the Transvaginal Mesh MDLs have been scheduled to start in December 2013. Defendants in the first three bellwether trials are American Medical Systems (AMS), Boston Scientific and Ethicon. (American Medical Systems is referred to as MDL 2325).

 

FDA Adverse Incident Reports On the Vaginal Mesh

The FDA received more than 1,000 complaints associated with trans vaginal mesh between 2005 and 2007. That number almost tripled between 2008 and 2010.

The Vaginal Mesh stories of suffering go on and on with more women filing lawsuits every day. The Vaginal Mesh Helpline has a mission, We must locate all women suffering from these Prolene mesh implants after 2001 and get them to a mesh lawyer to file their transvaginal mesh lawsuit today.

Be aware that all these devices have fancy names but they are all mesh. If you have a Prolene product implanted in you for prolapse or urinary incontinence call the Vaginal Mesh Helpline today. It is most likely one of these mesh devices that women are  filing vaginal mesh lawsuits for nationwide. Be aware you must move quickly. Statute of limitations for states are running close. If you have a current mesh lawyer call today and get and update. Find out who has your vaginal mesh file. Many lawyers may have referred your case out. Find out if your lawsuit was filed. Since the mesh is now a consolidated MDL it is extremely easy for lawyers to file the lawsuits. The Bellwether trials will begin soon…Do not be left out. Stay on top of things. if you need help or have questions call the Vaginal Mesh Helpline today. If you have received a rejection letter from a law firm do not give up hope. call us about your vaginal mesh lawsuit today. We will make every attempt to locate a vaginal mesh lawyer for you to take your case. But, these must be mesh implanted after 2001, closer to 2002.