Bard Avaulta Mesh Side Effects

Bard Avaulta Mesh may carry side effects of infection, mesh erosion, or pelvic organ prolapse and attorneys are filing lawsuits on behalf of injured patients in the US.  Contact a Bard Avaulta Mesh attorney if you have been affected to discuss your legal options.

According to recent FDA warnings, Bard Avaulta surgical mesh devices may be linked to the development of significant side effects among patients, including surgical mesh infection, erosion, and recurrence of pelvic organ prolapse (POP) or stress urinary incontinence (SUI). Product manufacturing company, C.R. Bard, developed Bard Avaulta mesh as an alternative treatment for women suffering from POP and SUI, two debilitating conditions caused by weakened pelvic muscles. Unfortunately, Bard Avaulta side effect information has indicated that the surgical mesh product may be associated with side effects so severe they may significantly outweigh any possible benefits of the treatment. In fact, over the past three years, the FDA has received over 1,000 reports from nine surgical mesh manufacturers of complications that were associated with surgical mesh devices used to repair POP and SUI. If you have received a Bard Avaulta mesh implant and have since developed one or more side major effects, contact a Bard Avaulta mesh attorney to discuss your legal options.

Surgical Mesh Erosion

One of the most dangerous and frequently occurring side effects of surgical mesh devices is erosion of the mesh into the vagina. When this side effect occurs, it can lead to discomfort and serious pain for the patient, including pain during sexual intercourse. In order to treat this side effect, some patients require additional surgery to remove the defective device. Unfortunately, removal of surgical mesh can be extremely dangerous, since surgical mesh products like Bard Avaulta allow for tissue infiltration.

Surgical Mesh Infection

Once surgical mesh erodes into the vagina, urethra or bladder, the affected patient may also suffer from surgical mesh infection. This side effect is often accompanied by symptoms like pain with intercourse, vaginal pain and bleeding, malodorous vaginal discharge, generalized pain, and chronic bladder infections. If a surgical mesh infection occurs, the affected patient may require removal of the mesh, which can lead to severe complications like hemorrhage, scarring of the pelvic tissues and muscles, and permanent disfigurement.

Recurrence of Prolapse or Incontinence

In some cases, women who receive a transvaginal surgical mesh implant may suffer from recurrence of prolapse or incontinence, the two conditions the device is meant to treat. Pelvic organ prolapse (POP) occurs when a pelvic organ like the bladder drops from its normal position and pushes against the walls of the vagina. POP is most often caused by weakened muscles that hold the pelvic organs in place, which can result from childbirth or surgery. Stress urinary incontinence (SUI) is a type of incontinence caused by leakage of urine during moments of physical stress. According to the FDA, it is not clear that transvaginal POP repair with mesh is more effective than traditional non-mesh repair, and it may result in recurrence of the original problem.

FDA Warnings for Bard Avaulta Mesh Side Effects

In 2008, the FDA issued a safety announcement warning patients and physicians about the potential side effects of surgical mesh products like Bard Avaulta mesh. According to the FDA warning, the most frequent surgical mesh side effects included surgical mesh infection, erosion of the mesh into the vagina, recurrence of prolapse or incontinence, pain during sexual intercourse, and bladder, bowel and blood vessel perforation caused by the surgical tools used in the mesh placement procedure. According to the FDA, some instances of erosion and scarring of the vagina may lead to discomfort and pain, sometimes requiring additional surgery to remove the eroded mesh. In July 2011, the FDA issued an additional warning to the medical community, notifying patients and healthcare providers that serious complications associated with surgical mesh products like Bard Avaulta mesh are not rare, and that it is not clear that transvaginal POP repair with mesh is more effective than traditional non-mesh repair.

Bard Avaulta Mesh Attorneys for Side Effects

The side effects that may be linked to the transvaginal placement of surgical mesh are serious and can lead to severe pain and suffering for affected patients. If you or a loved one has suffered from an alleged Bard Avaulta mesh side effect, contact an experienced Bard Avaulta mesh attorney to discuss your options for legal recourse. You may have grounds to file a Bard Avaulta mesh lawsuit against C.R. Bard in order to seek financial compensation for your injuries, medical expenses, and pain and suffering. Medical device manufacturers like C.R. Bard are responsible for the safety and effectiveness of their products, and should be held accountable for any adverse side effects sustained by consumers of their products. Unfortunately, this isn't always the case. By hiring a qualified Bard Avaulta mesh lawyer, victims of potential Bard Avaulta mesh side effects can collect the compensation they deserve, and hold the allegedly negligent manufacturing company liable for its dangerous product.






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