FAQ: Do I Need A Transvaginal Mesh Attorney To File a Case?

Our Transvaginal Mesh attorney at TruLaw is dedicated to supporting clients throughout the process of filing a product liability lawsuit.

With proven success in handling similar cases, Jessica Paluch-Hoerman provides personalized guidance and advocacy to clients affected by transvaginal mesh complications.

Our team combines legal expertise with genuine care for each client’s unique situation.

We understand the physical and emotional challenges that transvaginal mesh complications bring to your life, which is why we focus on simplifying the legal process of seeking the compensation you deserve.

Meet the Lead Transvaginal Mesh Attorney at TruLaw

Meet our lead Transvaginal Mesh attorney:

• Jessica Paluch-Hoerman: With years of experience representing clients in product liability cases, Jessica specializes in simplifying the legal process of recovering damages for medical expenses, pain and suffering, and various other forms of damages. Her dedication to holding negligent parties accountable for their actions has led to over $3 Billion in compensation for her clients nationwide through verdicts and negotiated settlements.

How much does it cost to hire a Transvaginal Mesh lawyer from TruLaw?

At TruLaw, we believe financial concerns should never stand in the way of justice.

That’s why we operate on a contingency fee basis—with this approach, you won’t face any upfront costs for your legal representation.

Our fee is only collected if we are successful in securing compensation on your behalf.

This arrangement not only removes the financial risk of pursuing your case, it allows us to focus our resources on achieving a positive outcome in your case by:

• Court Filings and Legal Documentation: Handling all necessary paperwork, including filing fees and procedural documents, to ensure your case proceeds smoothly through the legal system.
• Research/Data Analysis: Dedicating resources to thoroughly investigate your case and gather the best possible evidence.
• Expert Testimony: Consulting with leading experts in the field to support your case and demonstrate the strength of your case to the court.
• Negotiations and Trial Preparation: Allocating resources to negotiate potential settlements and, if needed, preparing comprehensive trial strategies to present your case in court effectively.

Our investment in representing you demonstrates our unwavering commitment to seeking the compensation you deserve.

If you or a loved one experienced serious complications from transvaginal mesh, you may be eligible to seek compensation.

Contact TruLaw using the chat on this page to receive an instant case evaluation and determine whether you qualify to join others in filing a Transvaginal Mesh lawsuit today.

Vaginal mesh lawsuits have been filed nationwide by thousands of women who suffered severe health complications from these implant devices.

To date, settlements total approximately $8 billion for claimants across 48 states.

While most cases have been resolved, new claims continue to be filed in 2025 by women experiencing ongoing complications from surgical mesh procedures.

The Transvaginal Mesh Litigation Crisis Explained

The Transvaginal Mesh Litigation encompasses lawsuits filed against transvaginal mesh manufacturers for injuries, pain and suffering, and financial costs related to complications from these medical devices.

Surgical mesh, also known as pelvic mesh or vaginal mesh, is a medical device surgically implanted to treat pelvic organ prolapse (POP) or stress urinary incontinence (SUI) in women.

These conditions often develop after childbirth, menopause, or hysterectomy when pelvic floor muscles weaken.

The use of transvaginal mesh has been highly controversial in the medical community.

While initially touted as an effective treatment for urinary incontinence, thousands of women have reported serious complications and injuries after transvaginal mesh surgery, resulting in extensive litigation against manufacturers.

Following years of complaints and growing safety concerns, the US Food and Drug Administration (FDA) banned sales of all transvaginal mesh products for pelvic organ prolapse in April 2019.

The Evolution of Transvaginal Mesh Devices and Regulatory Oversight

Transvaginal mesh products were introduced to the market in the 1990s.

In 1996, these devices became eligible for FDA approval through the expedited 510(k) process, which permits approval without rigorous clinical trials if a device is deemed similar to previously approved products.

This regulatory pathway allowed numerous mesh products to enter the market without comprehensive safety testing.

The FDA timeline regarding surgical mesh for pelvic organ prolapse POP and stress urinary incontinence SUI includes:

• 2008: First Public Health Notification warning healthcare providers about potential risks
• 2011: FDA identified transvaginal mesh for POP as high-risk
• 2012: FDA ordered manufacturers to conduct post-market surveillance studies
• 2016: FDA reclassified transvaginal mesh for POP as class III (high risk)
• 2019: FDA ordered all manufacturers to stop selling mesh for transvaginal POP repair

Major Defendants in Transvaginal Mesh Litigation

Multiple medical device transvaginal mesh manufacturers have faced lawsuits over their products.

The primary defendants include:

• Ethicon (Johnson & Johnson): Manufacturer of Gynecare TVT, Gynecare Prolift, and other mesh products
• C.R. Bard, Inc.: Producer of Avaulta, Pelvilace, and other mesh systems
• American Medical Systems (Endo International): Creator of Perigee, Apogee, and Elevate systems
• Boston Scientific Corp.: Manufacturer of Pinnacle, Advantage Fit, and other mesh devices
• Coloplast Corp.: Producer of Restorelle, Novasilk, and other mesh products
• Cook Medical, Inc.: Manufacturer of Surgisis Biodesign products
• Neomedic: Producer of various mesh implant devices

Despite the completion of Multidistrict Litigation (MDL) proceedings for many transvaginal mesh cases, attorneys continue to investigate and file vaginal mesh lawsuits on behalf of injured clients.

While most plaintiffs have received compensation through the MDL process, new lawsuits are still being filed in state courts nationwide.

History of Transvaginal Mesh MDL Cases

By 2012, due to the surge in lawsuits, the Judicial Panel on Multidistrict Litigation (JPML) consolidated transvaginal mesh cases into separate MDLs based on the manufacturer.

This streamlined the judicial process for thousands of similar claims.

MDL is a legal procedure that consolidates multiple similar cases from different jurisdictions into one court to improve efficiency.

Unlike class actions, where all plaintiffs receive similar compensation, MDL settlements are individualized based on each plaintiff’s specific damages.

The most recent MDL for transvaginal mesh injuries was centralized in the US District Court for the Southern District of West Virginia under Judge Joseph Goodwin.

This MDL was closed in November 2022, with the remaining cases remanded back to their original state courts.

Since litigation began, manufacturers have paid over $8 billion in settlements and jury verdicts to women injured by defective transvaginal mesh devices.

Transvaginal Mesh Settlement Values Explained

Settlement amounts in vaginal mesh lawsuits vary widely depending on the individual’s specific injuries, complications, number of revision surgeries, and overall impact on quality of life.

Compensation is determined based on tangible and intangible losses (damages).

Affected women may receive compensation for:

• Medical expenses (past and future)
• Revision surgeries
• Lost wages and earning capacity
• Pain and suffering
• Emotional distress
• Loss of consortium
• Diminished quality of life
• Other severe complications

The average projected settlement value for transvaginal mesh lawsuits ranges between $150,000 and $400,000, though individual cases may result in significantly higher or lower amounts depending on specific circumstances.

If you or a loved one experienced serious complications from transvaginal mesh, you may be eligible to seek compensation.

Contact TruLaw using the chat on this page to receive an instant case evaluation and determine whether you qualify to join others in filing a Transvaginal Mesh lawsuit today.

Surgical mesh implants have been associated with numerous serious complications that form the basis of litigation.

These vaginal mesh complications often require additional surgeries, ongoing medical treatment, and can cause permanent disability.

Serious Complications Associated with Transvaginal Mesh

Common complications that may qualify for legal action include:

• Mesh erosion: The mesh wears through the vaginal wall or surrounding tissues
• Chronic Pain: Persistent pelvic, vaginal, or groin pain
• Infection: Recurring or severe infections at the implant site
• Organ Perforation: Damage to bladder, bowel, or other pelvic organs
• Bleeding: Abnormal vaginal bleeding
• Sexual Dysfunction: Pain during intercourse (dyspareunia)
• Urinary Problems: Incontinence, retention, or frequent infections
• Nerve Damage: Resulting in chronic pain or numbness
• Mesh Shrinkage: Contraction causing pain and organ displacement
• Vaginal scarring: Formation of scar tissue that can cause pain and dysfunction
• Failed Repair: Recurrence of prolapse or incontinence

Recent scientific research has raised additional concerns about the material used in these implants.

A 2024 University of Sheffield study revealed that polypropylene mesh begins to degrade within 60 days of implantation, with further deterioration by 180 days.

This degradation contributes to inflammation, tissue damage, and persistent pain.

Recognizing Symptoms of Mesh Complications

Patients who have undergone mesh surgery should be aware of symptoms that may indicate complications:

• Persistent pelvic, vaginal, or groin pain
• Pain during intercourse
• Vaginal bleeding or discharge
• Recurrent urinary tract infections
• Difficulty urinating or bowel movements
• Visible mesh through the vaginal wall
• Fever or other signs of infection
• Return of pelvic organ prolapse or urinary incontinence symptoms

Early recognition of these symptoms is essential for appropriate medical intervention and may strengthen potential legal claims.

While many transvaginal mesh cases have been resolved, attorneys continue to accept new clients who have suffered injuries from these devices. Knowing the eligibility criteria can help determine if you have a valid claim.

Key Factors in Transvaginal Mesh Lawsuit Qualification

To qualify for a vaginal mesh lawsuit, several factors must be established:

1. Documented Mesh Implant: Medical records confirming the implantation of a transvaginal mesh device
2. Timing Considerations: The date of mesh surgery and discovery of complications may affect the statute of limitations
3. Serious Complications: Evidence of significant complications requiring medical intervention
4. Causation: Establishing that the mesh device caused the injuries
5. Manufacturer Liability: Determining the responsible manufacturer and their potential negligence

An experienced transvaginal mesh attorney can evaluate these factors to determine eligibility for legal action. Many law firms offer free consultations to assess potential claims.

Building a Strong Transvaginal Mesh Case

Compelling medical evidence is essential to building a successful vaginal mesh lawsuit.

Important medical documentation typically includes:

• Medical Records: Detailed documentation of the transvaginal mesh surgery procedure
• Treatment History: Records of complications, additional surgeries, and ongoing treatment
• Expert Testimony: Medical opinions linking injuries to the mesh device
• Financial Documentation: Evidence of medical expenses, lost wages, and other economic damages
• Personal Impact Statement: Documentation of how the injuries have affected quality of life

Your attorney will help gather and organize this evidence to build the strongest possible case against the manufacturer.