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Bard Avaulta Mesh Complications

bard avaulta

Bard Avaulta Transvaginal Mesh Complications Lawsuit

Bard Avaulta Transvaginal Mesh Complications, Side Effects, Lawsuit | Transvaginal Mesh, Pelvic Mesh, Surgical Mesh, Pelvic Sling | Lawsuits, Lawyer, Attorney | Side Effects: Bleeding, Pelvic Pain, Infection, Surgical Mesh Infection, Vaginal Epithelium Erosion, Erosion of Vaginal Tissue, Mesh Erosion, Pain, Incontinence, Urinary Problems, Prolapse, Bowel Perforation, Bladder Perforation, Blood Vessel Perforation, Pressure or “fullness” in the lower abdomen, Dyspareunia, Painful Sexual Intercourse, Vaginal bleeding Vaginal infections, Vaginal pain not related to intercourse, Vaginal Scarring, Neuropathic Numbness Or Weakness | Impaired Healing, Complications, Revision Surgery For Pelvic Organ Prolapse (POP) or Stress Urinary Incontinence (SUI)

If you received the C.R. Bard Avaulta mesh system during surgery to repair pelvic prolapse or treat urinary incontinence, you may be at risk for erosion, extrusion, hardening and shrinkage of the mesh materials. This can cause severe and persistent pain, infection and the need for additional surgical procedures to remove the Bard Avaulta mesh.

A growing number of lawsuits over the Bard Avaulta vaginal mesh have been filed in courts throughout the US. These lawsuits allege that C.R. Bard was negligent in the product’s design and in failing to warn patients of possible complications with Bard Avaulta mesh. Some doctors have also been named in these lawsuits, which also claim that the Bard Avaulta mesh was improperly and negligently implanted in patients.

It is believed that the Bard Avaulta surgical mesh design inhibits surrounding tissue from receiving nutrients and oxygen, causing impaired healing. This can lead to complications that may require further surgery.

Possible Bard Avaulta Complications and Injuries:

  • Erosion of the mesh through the vaginal tissue
  • Exposure or extrusion of mesh, which can require multiple surgeries
  • Feeling a lump in the vaginal opening or something protruding from vagina
  • Painful sexual intercourse
  • Perforation or puncture of the bladder, intestines and bowels, as well as blood vessels around the vaginal wall
  • Recurrent Pelvic Organ Prolapse (POP)
  • Recurrent Stress Urinary Incontinence (SUI)
  • Urinary problems
  • Vaginal bleeding
  • Vaginal chronic drainage, discharge and infections
  • Vaginal pain
  • Vaginal scarring and shortening

Complete Bard Avaulta mesh removal often requires multiple surgical procedures and results in scarring of pelvic tissue and muscles. Unfortunately, complications from the implantation of a Bard Avaulta mesh can lead to a serious decline in the patient's quality of life.

C.R. Bard Avaulta MultiDistrict Litigation (MDL)

In October 2010, the U.S. Judicial Panel on Multidistrict Litigation consolidated all federal lawsuits involving C.R. Bard's Avaulta Biosynthetic, Avaulta Plus and Avaulta Solo transvaginal mesh products in a multidistrict litigation (MDL), the Avaulta Pelvic Support Systems Product Liability Litigation (MDL 2187). The C.R. Bard Avaulta MDL is currently pending in U.S. District Court, Southern District of West Virginia before the Honorable Joseph R. Goodwin. Plaintiffs with lawsuits pending in the C.R. Bard Avaulta MDL allege that these surgical mesh devices were defectively designed and caused them to sustain serious injuries, including erosion, extrusion, dyspareunia, and pain. Plaintiffs further allege the defendants failed to warn of the extent and types of injuries, or that the discomfort caused by transvaginal mesh complications could be permanent, even after multiple corrective surgeries.

An MDL allows lawsuits associated with a particular product to be coordinated under one judge for pretrial litigation to avoid duplicative discovery, inconsistent rulings and to conserve the resources of the parties, witnesses and the court. When lawsuits are consolidated as a multidistrict litigation, each retains its own identity. If lawsuits in the C.R. Bard Avaulta MDL are not resolved, they will be transferred back to the court where they originated for trial.

Legal Help For Victims Affected By Bard Avaulta Mesh Complications

If you are among the women suffering because of the Bard Avaulta mesh, we can help. For a free legal consultation with one of our defective medical device attorneys, please fill out our online form or call 1-800-YOURLAWYER (1-800-968-7529).


Bard Avaulta Mesh ComplicationsRSS Feed

Bard Request to Exclude Internal Memos From Avaulta Vaginal Mesh Injury Trial Denied

Jan 16, 2014
A federal judge has ruled that device maker, C.R. Bard, must include internal memos concerning its now-recalled Avaulta pelvic mesh product in a bellwether product liability trial. C.R. Bard asked Judge Joseph Goodwin of the U.S. District Court for Southern Western Virginia to exclude six internal memos authored by Bobby Or, head of Bard's Advanced Surgical Concepts division, according to The memos were written in 2008 and 2009 and involved a number of choices and materials...

Tennessee Woman Says that Transvaginal Mesh Manufactured by C.R. Bard, Boston Scientific Caused Injuries; Lawsuit Alleges that the Pelvic Devices are Defective

Sep 18, 2012 | Parker Waichman LLP
Download FDA Update on the Serious Complications Associated with TVM Parker Waichman LLP, a national law firm dedicated to protecting the rights of victims injured by defective medical devices, has filed a lawsuit on behalf of a woman who suffered a serious injury, allegedly due to two transvaginal mesh products manufactured by Defendants C.R. Bard, Inc. and Boston Scientific Corporation. The suit was filed on July 12th in the U.S. District Court for the Southern District of West...

Kentucky Woman Implanted with C. R. Bard's Transvaginal Mesh Alleges that the Pelvic Devices Caused Painful, Permanent Injuries

Sep 12, 2012 | Parker Waichman LLP
Parker Waichman LLP, a national law firm dedicated to protecting the rights of victims injured by defective medical devices, has filed a lawsuit naming C.R. Bard, Inc. as Defendants. The suit alleges that two transvaginal mesh implants manufactured by the company caused serious injuries to a Kentucky woman. Parker Waichman filed the suit on July 12th in the U.S. District Court for the Southern District of West Virginia, Charleston Division (Case No. 2:12-cv-03106) where it is one of many...

Bard Avaulta Mesh Lawsuits Set for First Bellwether Trial

May 3, 2012 | Parker Waichman LLP
Litigation over C.R. Bard's Avaulta transvaginal mesh devices is moving ahead.  According to a report from Bloomberg News, the federal judge overseeing the Bard Avaulta transvaginal mesh multidistrict litigation has scheduled the first bellwether trial for February 3, 2013.About 600 Bard Avaulta transvaginal mesh lawsuits are pending in the multidistrict litigation before U.S. District Judge Joseph R. Goodwin.  Judge Goodwin is also overseeing multidistrict litigations involving other...

Transvaginal Mesh for POP Repair Should be Classified "High Risk," FDA Panel Says

Sep 9, 2011 | Parker Waichman LLP
An advisory panel for the U.S. Food & Drug Administration (FDA) voiced support for an agency proposal to reclassify transvaginal mesh devices used to repair pelvic organ prolapse (POP)  as high risk, or Class III.  If the FDA does go forward with the change, manufacturers of  would be required to conduct premarket clinical trials of transvaginal mesh devices before they could be marketed for POP surgery.Currently, transvaginal mesh devices are marketed as moderate risk, or...

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