Transvaginal Mesh (TVT / TVM) Attorneys

FREE NATIONWIDE CASE EVALUATIONS: CALL 1-800-632-1404

WARNING: There have been more than 1,000 suspected injuries as a result of defective design, manufacturing and testing of transvaginal mesh / TVM / TVT devices. To speak to an attorney today, please call us or fill out the form to the right.

About The Lawsuit

On October 20, 2008 the U.S. Food & Drug Administration (FDA) issued an urgent public health notification to physicians and patients regarding serious complications associated with transvaginal placement of surgical mesh in repair of Pelvic Organ Prolapse (POP) and Stress Urinary Incontinence (SUI). Incredibly, over at least the last three years, the FDA has received over 1,000 reports from at least nine surgical mesh manufacturers regarding serious complications related to the placement and use of transvaginal mesh products. We are here to try and help you after you have likely endured pain and suffering from these medical products.

Injuries

There are a variety of injuries associated with the transvaginal mesh, TVM and TVT device.  Some recipients experience pain almost immediately, but others develop pain over time, including a different pain that develops after the initial pain of surgery begins to wear off.  Some of our clients have reported the following symptoms and injuries:

  • Erosion of vaginal tissue
  • Infection
  • Pain
  • Urinary problems
  • Recurrence of Pelvic Organ Prolapse (POP) and Stress Urinary Incontinence (SUI)
  • Perforations of the bowel, bladder or blood vessels
  • Vaginal scarring
  • Mesh erosion

Many times, sexual intercourse is impossible, and daily chores such as walking up stairs can seem impossible.  You could be losing time away from work, or time away from your family and friends. You also may have experienced numerous revision or repair surgeries, some of which resulted in there being mesh left inside of you.  We have clients who have suffered from these very problems. You are not alone, and we would encourage you to call us for help.

Reports of Transvaginal Mesh Complications

Since 2005, more than 1,000 patients have suffered from serious complications from the placement of a transvaginal mesh device. The transvaginal mesh is a type of medical device used to treat Pelvic Organ Prolapse (POP) and Stress Urinary Incontinence (SUI), conditions that may occur after childbirth and pregnancy. If you or someone you loved has been injured, you have the legal right to pursue monetary compensation in a court of law.

In October 2008, the FDA issued a public health notification alerting healthcare providers and the public to the increasing number of serious health issues associated with the transvaginal mesh. Complications reported to the FDA include meshes from nine different manufacturers. Transvaginal meshes are implanted through surgery. According to the FDA, contributing factors to complications potentially include the patient’s health, mesh material, the size and shape of the mesh, surgical procedures and estrogen levels.

You can read the FDA Notice by clicking [HERE].

FDA Video

Manufacturers

Defective transvaginal mesh products are designed and manufactured by a number of companies under a wide array of trade names.  Manufacturers of transvaginal mesh products include:

  • American Medical Systems
  • Bard
  • Boston Scientific
  • Ethicon
  • Gynecare
  • Johnson & Johnson

After calling our office, we will assist with obtaining the necessary records required for investigating a claim against one of these device manuacturers.

No Recovery, No Fee

We take transvaginal mesh / TVM and TVT litigation cases on a contingency basis. That means that there is no cost to you unless we and our co-counsel are able to recover a settlement or judgment on your behalf. So, unless your case is resolved by trial, arbitration, settlement, or other resolution, you do not have to pay any attorney fees to us, or pay any costs. Litigation costs include filing fees, court reporter fees for deposition, copying costs, experts, and travel. Litigation costs are paid by our firm so you don’t have to have cash to pursue justice against medical device corporations.

About us

Ed Wallis is one attorney in our firm that has been retained by clients across the country as to allegedly defective transvaginal mesh, TVM and TVT devices.  Along with Tim Edwards, Mr. Wallis is representing patients around the globe for the allegedly defective Advanced Bionics HiRes90k cochlear implant device.  They are honored to represent clients from multiple countries including in Europe, North America and South America.

As transvaginal mesh attorneys, TVM attorneys and TVT attorneys, we will investigate your claim and with our co-counsel we stand ready to push your case ahead.

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Please read our DISCLAIMER

CLICK THE REPORT ABOVE FOR A FREE REPORT: TEN THINGS EVERY PERSON WITH AN ADVANCED BIONICS COCHLEAR IMPLANT FAILURE SHOULD KNOW




CLICK EACH AREA FOR MORE INFORMATION.

Business Litigation

Probate Litigation

Qui Tam and Whistleblower Litigation

Pharmaceutical Litigation

Medical Device Litigation

Cochlear Implant Litigation

ASR DePuy Hip Implant System Recall Help

Wellbutrin Heart Defect and Birth Defect

Transvaginal Mesh Injuries

Fosamax Femur Fractures



ADVANCED BIONICS COCHLEAR IMPLANT RECALL

If you were the recipient of an Advanced Bionics Model HiRes90k cochlear implant and have sustained physical or emotional injuries as a result of the recall of this medical device, please call our team of lawyers today at 1-800-632-1404 or send us an E-MAIL today. You can also visit the COCHLEAR IMPLANT LITIGATION PAGE for more information on the HiRes90k recall.



WELLBUTRIN HEART DEFECTS AND BIRTH DEFECTS

A recent study published in the American Journal of Obstetrics and Gynecology suggests that women who take Wellbutrin during early pregnancy may run a greater risk for having a child born with a heart birth defect, including left outflow heart defects. If you took Bupropion hydrochloride, Wellbutrin®, Wellbutrin XL®, and Wellbutrin XR® and your child was born with a birth defect, please call Tim Edwards or Ed Wallis at 1-800-632-1404 or send us an E-MAIL today. You can also visit the WELLBUTRIN HEART DEFECT INFORMATION PAGE for more information.



QUI TAM AND WHISTLEBLOWER LITIGATION

American workers view improper and illegal acts at their jobs daily. The federal government has enacted laws to encourage workers to come forward and help disclose improper actions via qui tam and whistleblower claims, including via the False Claims Act and the Medicare False Claims Act. If you have knowledge of improper business practices and are willing to serve as a representative for the government, you are entitled to a share of any proceeds that are received by the government. We are willing to be your voice in helping you. Please call our team of False Claims Act attorneys at 1-800-632-1404 or send us an E-MAIL today. You can also visit the Qui Tam and Whistleblower Litigation Page for more information.

Super Lawyer

Mid South Trial Lawyer Tim Edwards is a Super Lawyer. Call him today at (800) 632-1404.

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