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Victims Who’ve Suffered From Transvaginal Mesh Implant Failures That Have Required Revision Or Replacement May Be Able To Seek Both Justice And Compensation

Victims Who’ve Suffered From Transvaginal Mesh Implant Failures That Have Required Revision Or Replacement May Be Able To Seek Both Justice And Compensation

Those Affected Who Meet The Following Guidelines May Qualify For A Free Case Evaluation And Compensation:

  • Transvaginal Mesh To Have Been Implanted Between 2008 - 2016
  • Implant Failure, Injury, Or Complication THAT REQUIRED Revision Or Replacement Surgery
  • Those Who Have NOT Previously SETTLED A Transvaginal Mesh Claim
  • Those Who Do NOT Currently Have An OPEN Case With An Attorney

Limited Time To File A Claim. Check Eligibility Today.


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How Faulty Transvaginal Mesh Implanting Leads To Serious Complications And Conditions


Transvaginal mesh is a synthetic net-like substance–typically constructed from polypropylene plastic–that is inserted to provide support to repair a damaged vaginal wall, support the urethra, fix pelvic organ prolapse (POP), or fix stress urinary incontinence (SUI).

Doctors deem the mesh to be “transvaginal” because the implant procedure goes through the vagina in what can often be a complicated, lengthy surgery–the procedure is also one that has the potential for serious problems if done improperly or if the mesh material itself is faulty.

A few of the more serious conditions linked to transvaginal mesh implants may include:

  • Pain and bleeding
  • Infections and scarring
  • Bowel, bladder, or blood vessel perforation
  • Lower back pain 
  • Chronic vaginal drainage
  • Additional reparatory surgeries

According to a Yale Medicine report “The Food and Drug Administration (FDA) recently halted sales of surgical mesh devices used for transvaginal repair of pelvic organ prolapse (POP).

“The FDA said that the manufacturers of the devices used for this type of pelvic organ prolapse repair had not demonstrated a reasonable assurance of their safety or effectiveness by the FDA deadline.

Reports and Studies Link Faulty Transvaginal Mesh Implant Cases On The Rise


According to a Mayo Clinic website report “Each use of mesh carries its own risks and benefits.

“Use of surgical mesh through the vagina to treat POP has been associated with higher rates of mesh-related complications, including mesh poking through the vaginal skin, pelvic pain, and pain with intercourse.

“In 2019, the FDA ordered manufacturers of surgical mesh for the transvaginal repair of POP to stop selling and distributing their products in the U.S.

“If you've had transvaginal mesh placed for the surgical repair of POP, continue with your routine care. If you have complications or symptoms, talk to your doctor.”

Complications reported in lawsuits against the manufacturers—which have resulted in nearly $8 billion in settlements to 100,000 women—include:

  • Bleeding;
  • Pain;
  • Inflammation; and,
  • Infections.

The Shield Legal Online team believes that victims of faulty transvaginal mesh implants should be able to address the doctors and institutions that were allegedly the source of the faulty surgeries and get compensation and justice.

Our network of attorneys have a track record of success.


Answer a brief, private online questionnaire that asks for key details of the experience


Have the case evaluated by a legal team free of charge without any obligation to file


Contact us right away to set up a free and confidential case review. 

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