Transvaginal Mesh Litigation

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Transvaginal Mesh Lawsuit

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Transvaginal Mesh?

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Transvaginal Mesh Lawsuits

Complications that have been reported by transvaginal mesh patients include pain, bleeding, infection, organ perforation, erosion through the vagina and urinary problems. Mesh erosion is the most common problem associated with transvaginal mesh, and in some cases cannot be fixed. Some women might also experience pain during intercourse and emotional problems.

The FDA also noted that many cases of POP can be treated without using surgical mesh, and that surgeons should carefully weigh the risks and the benefits for each individual patient.

Women with POP, who have been treated with surgical mesh, might be eligible to file a transvaginal mesh lawsuit if they have suffered serious complications following surgery. Our attorneys are reviewing potential lawsuits for women nationwide and would like to help you.

We believe that you should be compensated for your pain, suffering and debilitating injuries. If you would like to speak with a lawyer in a free and confidential consultation, please contact us today. We will listen to your story and let you know how we can help you.

Call today to schedule a free review of your case.

Transvaginal Mesh Complications

Transvaginal mesh has been linked to serious injuries and complications in a number of patients. In fact, the public advocacy group Public Citizen urged the U.S. Food and Drug Administration (FDA) to ban the use of all transvaginal mesh products that are used to treat pelvic organ prolapse (POP) on Aug. 25, 2011.

POP is a condition that occurs in approximately 30 to 50 percent of women after childbirth. The stress of childbirth can weaken the muscles and tissue that surround organs such as the uterus, bladder, bowel and top of the vagina.

When the supporting tissue and muscles are weakened, the organs can bulge or prolapse into the vagina or in some cases, beyond the wall of the vagina. POP has been treated surgically for years. In 2002, the FDA approved the use of surgical mesh to reinforce the tissue after surgically reinforcing the organs back into place.

The FDA issued a safety communication on July 13, 2011 to notify health care providers that the serious complications associated with surgical mesh to treat POP are "not rare." According to the agency, it has received 1,503 reports of complications with surgical mesh in POP patients from Jan. 1, 2008 to Dec. 31, 2010.

Top News

Boston Scientific Faces Thousands of Vaginal Mesh Lawsuits

December 19th, 2013

As transvaginal mesh lawsuits against device maker Boston Scientific Corp. begin to move forward, the company has been directed to bring... read more

J&J Accused of Destroying Vaginal Mesh Documents

December 10th, 2013

As Johnson & Johnson gears up for the first federal vaginal mesh trial, the company faces allegations of destroying or misplacing... read more

Transvaginal Mesh Lawsuit against Boston Scientific to Begin in January 2015

December 4th, 2013

According to reports, a transvaginal mesh lawsuit filed on behalf of a woman who alleges injuries following surgery to correct pelvic... read more

Last Bellwether C.R. Bard Transvaginal Mesh Lawsuit Scheduled for Today

December 3rd, 2013

The latest C.R. Bard transvaginal mesh lawsuit is scheduled for today in the U.S. District Court in West Virginia. This lawsuit... read more

FDA Discusses Risk of Using of Surgical Mesh for POP

August 29th, 2011

The U.S. Food and Drug Administration (FDA) discusses the risks associated with use of transvaginal mesh.

"There are clear risks associated with... read more

Some Doctors Avoid Transvaginal Mesh to Treat POP

August 25th, 2011

In recent years, surgeons have used a device called surgical mesh to support the organs of a woman's pelvis that have... read more

Problems with POP Mesh Surgery Cause Clinical Trial to End Early

August 2nd, 2011

Complications with a medical device used to reinforce the vaginal wall for pelvic organ prolapse (POP) forced researchers to end a... read more