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Mentor ObTape Vaginal Sling

ObTape

Mentor ObTape Vaginal Sling Side Effects May Result In Vaginal Extrusion Lawsuits

Mentor ObTape Vaginal Sling | Lawsuits, Lawyers | Side Effects: Impaired Healing, Vaginal Extrusion, Urinary Tract Erosion | Design Blocked Oxygen, Faulty Design, Defective Medical Device

The Mentor ObTape Vaginal Sling is a medical device manufactured to surgically treat female stress urinary incontinence.  Stress urinary incontinence affects about 13 million people, mostly women.  The embarrassing loss of bladder control caused by this condition can have a huge impact on a patient’s quality of life.

The Mentor ObTape Vaginal Sling transobturator device is an artificial structure that is designed to replace eroded or weakened muscles in the urethra. A vaginal sling is essentially a hammock for the vaginal wall, which is secured under the bladder to help support it. The intention is to reinforce the muscles that control the flow of urine from the body.The vaginal sling technique has been around for about 100 years, and is considered the gold standard” in stress urinary incontinence treatment. Generally, the minimally invasive treatment can be done on an outpatient basis.

But the Mentor ObTape Vaginal Sling did not work as intended.  Many women have had adverse reactions to the device including impaired healing, vaginal extrusion and urinary tract erosion that manifested itself in extreme vaginal pain, vaginal discharge, and infections.   The non woven design of the Mentor ObTape Vaginal Sling blocked much needed oxygen and nutrients while woven vaginal slings produced by other companies allow oxygen and nutrients to pass through.

ObTape Vaginal Sling Removed from Market

Not long after it was introduced, patients with the Mentor ObTape began to exhibit serious complications, including vaginal extrusion and urinary tract erosion, extreme vaginal pain, vaginal discharge, and infections. A study published in the October 2006 Journal of Urology discussed the widespread nature of the injuries caused by the Mentor ObTape Vaginal Sling. The study involved 67 women who had been implanted with the Mentor ObTape Vaginal Sling. Of those, more than 13 percent developed vaginal extrusions. Another eight developed a chronic vaginal discharge, and one patient developed an abscess of the left thigh that tracked to the incision site.  The study compared these patients to 56 others who had received another brand of vaginal sling.  None of those patients experienced the complications seen with the Mentor ObTape Vaginal Sling.

Within 3 years of the Mentor ObTape Vaginal Sling going on the market in 2003 the defective medical device was removed. The impact the OB Tape Vaginal Sling had on the lives of those women who were experienced complications was devastating as many experienced crippling pain and permanent scarring (vaginal erosion) damage from the procedures involved in the insertion and necessary removal of the device. The device failed to treat the female urinary stress incontinence in many women that it was implanted in.

Legal Help For Victims Affected By Mentor ObTape Vaginal Sling

If you or a loved one has had the Mentor ObTape Vaginal Sling implanted and had complication you may be entitled to compensation.  Please contact our experienced defective medical device attorneys for a free Mentor ObTape Vaginal Sling lawsuit case review by calling 1-800-YOURLAWYER or by filling out the form to the right.



 

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Vaginal Mesh Complications Halt Clinical Trial

Oct 25, 2010 | Parker Waichman LLP
Vaginal mesh may not be the best choice for repairing pelvic organ prolapse, according to an article published in the journal Obstetrics & Gynecology. According to the article, a clinical trial involving vaginal mesh was halted early because women who received the mesh had a far higher rate of complications compared to those who underwent a more traditional procedure called colpopexy. In October 2008, the US Food & Drug Administration (FDA) warned that the use of vaginal mesh to...

Mentor ObTape Lawsuits Proceeding

Apr 7, 2010 | Parker Waichman LLP
Legal action on behalf of women injured by the Mentor ObTape Vaginal Sling is proceeding with four cases scheduled for trial in California. In an order dated March 30, 2010, the California Superior Court denied Mentor Corporation’s motions to dismiss in four of the lawsuits, refusing to dismiss two of the cases on statute of limitations grounds. Johnson and Johnson now own Mentor. The Mentor ObTape is a transobturator vaginal sling used in thousands of women between 2003 and 2006 to...

Mentor ObTape Fast-Track Approval Questioned

May 5, 2009 | Parker Waichman LLP
A new report is raising questions about the fast-track approval of the Mentor ObTape.  According to The New York Times, the device has become the subject of numerous lawsuits since Mentor Corporation removed it from the market in 2006.The Mentor ObTape, used to treat stress urinary incontinence, is designed to replace eroded or weakened muscles in the urethra and is essentially a hammock for the vaginal wall. The vaginal sling technique has been around for about 100 years and is considered...

FDA Warns of Complications with Surgical Mesh

Jan 9, 2009 | Parker Waichman LLP
Download FDA Update on the Serious Complications Associated with TVM The Food & Drug Administration (FDA) recently warned that surgical mesh used in gynecologic surgery to treat pelvic organ prolapse and stress urinary incontinence had been linked to serious complications.  As we've reported previously, one such type of surgical mesh, the Mentor ObTape Vaginal Sling, was withdrawn from the market in 2006 because of a high rate of serious complications.According to the FDA, in the...

Transvaginal Placement of Surgical Mesh Linked to Painful Complications

Oct 22, 2008 | Parker Waichman LLP
Download FDA Update on the Serious Complications Associated with TVM Transvaginal placement of surgical mesh has caused serious complications, the Food & Drug Administration (FDA) warned yesterday.  According to the agency, treatment of these complications can be painful and require further surgery (some for mesh removal), intravenous therapy, blood transfusion, or hematoma/abscess drainage.  The FDA has advised that clinicians should receive specialized training for the...

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