Sandy Liebhard

Vaginal mesh complications have prompted thousands of lawsuits that continue to progress in federal multidistrict litigations currently underway in the U.S. District Court, Southern District of West Virginia. In March, the judge overseeing these proceedings issued an Order that designated four Avaulta mesh implant lawsuits for the first trials to be heard in the litigation established for the C.R.

Providing information for woman who have received vaginal mesh implants and have experienced serious vaginal mesh complications. The FDA has expressed growing concern about the dangers associated with transvaginal mesh and demand for a possible vaginal mesh recall continues to grow. To find out if you qualify to file a vaginal mesh lawsuit, contact a vaginal mesh lawyer at Bernstein Liebhard LLP for a free and confidential case evaluation.

Suffering from vaginal mesh complication and you need Legal Help for Injury to File a vaginal mesh lawsuit Injury.

Suffering from vaginal mesh complication and you need Legal Help for Injury to File a vaginal mesh lawsuit Injury. Our vaginal mesh lawyer helps you .call 888-364-6688 or visit us to arrange a free case review

Providing information for woman who have received vaginal mesh implants and have experienced serious vaginal mesh complications.

Providing information for woman who have received vaginal mesh implants and have experienced serious vaginal mesh complications. The FDA has expressed growing concern about the dangers associated with transvaginal mesh and demand for a possible vaginal mesh recall continues to grow.

Suffering from Vaginal mesh complications arranges a free case

Suffering from Vaginal mesh complications arranges a free case Providing information for woman who have received vaginal mesh implants and have experienced serious vaginal mesh complications.

Providing information for woman who have received vaginal mesh implants and have experienced serious vaginal mesh complications. The FDA has expressed growing concern about the dangers associated with transvaginal mesh and demand for a possible vaginal mesh recall continues to grow.

A leader in litigating cases involving defective medical devices, dangerous drugs and consumer products, Bernstein Liebhard LLP is a New York-based law firm that has been exclusively representing injured persons in complex individual and class action lawsuits nationwide since 1993.

Thousands of women who allegedly suffer from serious and painful vaginal mesh complications following procedures to treat pelvic organ prolapse (POP) and stress urinary incontinence (SUI) are now seeking legal recourse via vaginal mesh lawsuits. These women allege the devices are defective and put recipients at increased risk for serious injuries. Yet despite mounting legal claims and reports of significant injuries associated with the mesh, most device manufacturers have yet to implement a vaginal mesh recall.

Thousands of women who allegedly suffer from serious and painful vaginal mesh complications following procedures to treat pelvic organ prolapse (POP) and stress urinary incontinence (SUI) are now seeking legal recourse via vaginal mesh lawsuits.

Thousands of women who allegedly suffer from serious and painful vaginal mesh complications following procedures to treat pelvic organ prolapse (POP) and stress urinary incontinence (SUI) are now seeking legal recourse via vaginal mesh lawsuits. These women allege the devices are defective and put recipients at increased risk for serious injuries. Yet despite mounting legal claims and reports of significant injuries associated with the mesh, most device manufacturers have yet to implement a vaginal mesh recall.

Thousands of women who allegedly suffer from serious and painful vaginal mesh complications following procedures to treat pelvic organ prolapse (POP) and stress urinary incontinence (SUI) are now seeking legal recourse via vaginal mesh lawsuits. These women allege the devices are defective and put recipients at increased risk for serious injuries. Yet despite mounting legal claims and reports of significant injuries associated with the mesh, most device manufacturers have yet to implement a vaginal mesh recall.

Thousands of women who allegedly suffer from serious and painful vaginal mesh complications following procedures to treat pelvic organ prolapse (POP) and stress urinary incontinence (SUI) are now seeking legal recourse via vaginal mesh lawsuits. These women allege the devices are defective and put recipients at increased risk for serious injuries. Yet despite mounting legal claims and reports of significant injuries associated with the mesh, most device manufacturers have yet to implement a vaginal mesh recall.

A Public Broadcasting Service (PBS) "Need to Know" series recently discussed vaginal mesh complications, which have affected thousands of women implanted with the controversial medical devices. PBS correspondent, Dr. Emily Senay, spoke with Linda Gross of South Dakota who experienced serious and devastating vaginal mesh complications she says have changed her family, her life, and her career.

A Public Broadcasting Service (PBS) "Need to Know" series recently discussed vaginal mesh complications, which have affected thousands of women implanted with the controversial medical devices. PBS correspondent, Dr. Emily Senay, spoke with Linda Gross of South Dakota who experienced serious and devastating vaginal mesh complications she says have changed her family, her life, and her career.

A Public Broadcasting Service (PBS) "Need to Know" series recently discussed vaginal mesh complications, which have affected thousands of women implanted with the controversial medical devices. PBS correspondent, Dr. Emily Senay, spoke with Linda Gross of South Dakota who experienced serious and devastating vaginal mesh complications she says have changed her family, her life, and her career. With the help of experienced vaginal mesh lawyers, Gross was able to obtain compensation for her injuries. But thousands of women still await their day in court.

Our firm regularly hears from women who suffered significant vaginal mesh complications, allegedly due to pelvic mesh devices manufactured by C.R. Bard and other manufacturers, so of course we are looking forward to these trials" says Bernstein Liebhard LLP, a nationwide law firm representing victims of defective drugs and medical devices.

Vaginal mesh lawyers continue to file lawsuits over alleged injuries caused by products manufactured by C.R. Bard, Inc. in New Jersey’s Atlantic County Superior Court, Bernstein Liebhard LLP reports. The litigation’s first bellwether trials are scheduled to begin on September 23, 2013, according to an April 25th Court Order.

Bernstein Liebhard LLP represents a number of women who have brought vaginal mesh lawsuits after suffering from serious vaginal mesh complications similar to those described in this study.

Bernstein Liebhard LLP represents a number of women who have brought vaginal mesh lawsuits after suffering from serious vaginal mesh complications similar to those described in this study.

Vaginal mesh lawyers at Bernstein Liebhard LLP report that an emerging study, recently presented at the Annual Congress of the European Association of Urology, revealed risk factors that may help determine which women are the likeliest to suffer from vaginal mesh complications, says Bernstein Liebhard LLP. The study looked at 677 women who had undergone pelvic organ prolapse (POP) repair with a trocar-guided transvaginal mesh device.

Vaginal mesh lawyers at Bernstein Liebhard LLP report that an emerging study, recently presented at the Annual Congress of the European Association of Urology, revealed risk factors that may help determine which women are the likeliest to suffer from vaginal mesh complications, says Bernstein Liebhard LLP. The study looked at 677 women who had undergone pelvic organ prolapse (POP) repair with a trocar-guided transvaginal mesh device. The research revealed an increased risk for injury in younger women, women diagnosed with less prominent prolapse, or women who had undergone a concomitant hysterectomy (hysterectomy with another procedure, likely the POP repair). Study participants suffered from significant injuries that included mesh erosion and shrinkage; pain during sexual intercourse; pelvic abscesses; and pelvic, vaginal, and perineal hematomas

Vaginal mesh implants emerged as a popular surgical treatment for Woman suffering from Pelvic Organ Prolapse ("POP") and Stress Urinary Incontinence ("SUI"). For many woman, multiple surgeries are often required to remove the mesh and even after corrective surgeries, a full recovery may not be possible.

Women who received vaginal mesh implants and have experienced complications following surgery with transvaginal mesh may qualify to file a vaginal mesh lawsuit seeking compensation for pain and suffering, medical bills, lost wages, and other damages. By filing a vaginal mesh lawsuit you will not be suing your doctor, but rather the manufacturers that defectively designed the mesh device as well as the companies that marketed the products and failed to warn about the serious risks. To date, litigation is currently pending against multiple vaginal mesh manufacturers including: American Medical Systems, Boston Scientific, Coloplast, C.R. Bard, and Johnson & Johnson.

Vaginal mesh complications can be extremely serious, painful, and even life threatening. Women who were implanted with vaginal mesh following surgical procedures for the treatment of stress urinary incontinence and pelvic organ prolapse have reported experiencing severe pain, infections, organ perforation, scarring, and erosion of the mesh. Often vaginal mesh complications require the need for multiple revision surgeries to remove the defective devices. To date, the FDA has received close to 3,800 reports of adverse events related to vaginal mesh