Bard Avaulta Mesh and Recurrence of POP and/or SUI Side Effects

Bard Avaulta mesh may be linked to a recurrence of Pelvic Organ Prolapse, POP, and Stress Urinary Incontinence, SUI in patients and Bard Avaulta Mesh lawsuits may be filed by attorneys across the US.  Contact an attorney if you have been adversely affected by Bard Avulta mesh.

The medical device called Bard Avaulta mesh, used to repair conditions like pelvic organ prolapse (POP) and stress urinary incontinence (SUI) in women, may be linked to severe side effects, including recurrence of POP and/or SUI. Bard Avaulta mesh is currently produced by manufacturing company C.R. Bard Inc., and is commonly used to treat POP and SUI in women. Unfortunately, recent research has suggested that Bard Avaulta mesh and other surgical mesh devices may be associated with serious side effects which may cause devastating and irreparable harm in patients. If you received a Bard Avaulta mesh implant and have since suffered from recurrence of prolapse and/or incontinence, contact a Bard Avaulta attorney to discuss your options for legal recourse.

Recurrence of Prolapse and/or Incontinence

Pelvic organ prolapse occurs when the tissues that hold the pelvic organs in place become weak or stretched, often after childbirth or surgery. When this happens, one or more pelvic organs may slip out of place and put pressure on the vagina, resulting in pain and sometimes incontinence. Stress urinary incontinence is a leakage of urine during moments of physical activity, including exercising, laughing, coughing or sneezing. Despite the fact that surgical mesh products like Bard Avaulta mesh were designed to repair POP and SUI, women who receive a transvaginal surgical mesh implant to treat these conditions may actually suffer from recurrence of prolapse and/or incontinence, in addition to other severe side effects.

Recurrence of POP and/or SUI Treatment and Prognosis

The side effects associated with surgical mesh devices, including recurrences of POP and/or SUI, may be significant enough to require removal of the defective mesh. Unfortunately, surgical mesh products like Bard Avaulta mesh are designed to allow for tissue infiltration, which makes it extremely dangerous to remove the mesh. Some women who undergo surgery to remove faulty mesh may experience life-altering side effects like permanent disfigurement, hemorrhage, and scarring of the pelvic muscles and tissues.

FDA Warnings Regarding Bard Avaulta Mesh Side Effects

The FDA issued a public health advisory in 2008 warning patients and healthcare professionals about the complications associated with transvaginal placement of surgical mesh to treat POP and SUI. According to the FDA warning, the previous three years had resulted in over 1,000 reports from nine surgical mesh manufacturers of complications associated with surgical mesh devices like Bard Avaulta mesh. The most frequent complication, the FDA reported, included surgical mesh erosion, surgical mesh infection, urinary problems, pain, and recurrence of prolapse and/or incontinence. In July 2011, the FDA issued an updated warning, notifying the public that serious complications associated with surgical mesh for transvaginal repair of POP are not rare. Furthermore, the agency declares that it is not clear that transvaginal POP repair with mesh is more effective than traditional non-mesh repair in all patients with POP, and may actually expose patients to greater risk.

Bard Avaulta Attorneys for Side Effects

Women suffering from pelvic organ prolapse or stress urinary incontinence depend on medical devices like Bard Avaulta mesh to effectively treat their condition without causing them any unnecessary harm. Unfortunately, the side effects potentially linked to Bard Avaulta mesh and other surgical mesh products are severe enough to possibly outweigh any benefits of the devices. If you or a loved one has suffered from POP and/or SUI recurrence, and you believe Bard Avaulta mesh to be the cause, contact an experienced Bard Avaulta mesh attorney to discuss your legal options. You may have grounds to file a Bard Avaulta mesh lawsuit against C.R. Bard Inc. in order to seek financial compensation for your injuries, medical expenses, and pain and suffering. You are not at fault for any injuries caused by a defective medical device. By hiring a qualified Bard Avaulta mesh lawyer to represent your case, you can collect the compensation you deserve and protect yourself and your family from further harm.






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