An estimated 75,000 women have undergone surgery for bladder leakage and pelvic organ prolapse (POP) using various vaginal mesh products that are now under federal scrutiny for causing serious complications.

A woman who has had vaginal mesh implanted during surgery and who experiences the following symptoms should see her doctor right away:

  • Fever
  • Bleeding
  • Pelvic pain
  • Vaginal discharge
  • Vaginal pain
  • Painful sexual intercourse
  • Recurrence of prolapse or incontinence
  • New onset of urinary incontinence

Bladder Leaks and Pelvic Organ Prolapse (POP)

Bladder leakage called Stress Urinary Incontinence (SUI) occurs when there is an involuntary loss of urine during physical activity such as, laughing, coughing, sneezing or exercising. Common causes of this condition include: childbirth, getting older, persistent cough or obesity. Stress urinary incontinence affects up to 40 percent of American women and is expected to increase as the U.S. population ages

POP occurs when the ligaments and muscles that hold the pelvic organs in place become so stretched and weakened that they cannot hold the pelvic organs in place and descend into the vagina. The most common organ to prolapse, or descend, is the bladder, but sometimes the rectum or uterus will prolapse into the vagina.

In 2010, approximately 300,000 women in the U.S. had surgery to repair POP, according to the FDA.

History of Problems

On July 13, the FDA issued an urgent public notice on the medical devices after receiving thousands of reports about painful complications. The agency reported it had received over 2,800 reports of complications between January 2008 and December 2010. It said serious complications associated with surgical mesh for transvaginal repair of POP are not rare. It advised healthcare providers that in most cases, POP can be treated successfully without mesh surgery.


Concerns Cross all Product Lines

Nine companies manufacture transvaginal mesh products, including Boston Scientific, Johnson & Johnson, C.R. Bard, Tyco Covidian and AMS.

Concerns are not limited to any single vaginal mesh product. Products currently on the market include the following:

  • Advantage™ Sling System
  • Lynx™ Suprapubic Mid-Urethral Sling System
  • Obtryx® Curved Single
  • Obtryx® Mesh Sling
  • Prefyx Mid U™ Mesh Sling System
  • Prefyx PPS™ System

Legal Help for Victims of Defective Vaginal Mesh Products

If you or a loved one underwent surgery to implant a vaginal mesh product and later developed serious complications, you have the right to hold manufacturers legally responsible. Although a lawsuit won’t ease suffering or permanent disability, it can help pay medical expenses, improve the chances for quality of life or compensate for income or other losses. An experienced vaginal mesh attorney with Janet, Jenner & Suggs can review your situation and advise you. All consultations are free of charge. You can contact us online or call us toll-free 1-877-my-advocates (1-877-692-3862) to discuss your case with one of our vaginal mesh injury lawyers today.




Rob Jenner

Robert Jenner brings to the My Advocates medical and legal team more than 26 years experience representing injured consumers nation-wide against the manufacturers of dangerous prescription drugs, defective medical devices, tainted blood products, and other unsafe products. Mr. Jenner has been honored by his peers for inclusion in “The Best Lawyers in America” and “Maryland’s Super Lawyers”(named in Top 50). READ FULL BIO

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