Transvaginal Mesh Class Action Lawsuit Updates: December 2025

Transvaginal Mesh Lawsuit Litigation Updates

September 22, 2025

• Illinois lawsuit filed: A woman from Tolono has initiated a federal case against American Medical Systems and Endo Pharmaceuticals, claiming that the Sparc Sling System led to mesh erosion, ongoing pain, and required additional corrective surgeries. The lawsuit alleges defects in design and manufacturing, inadequate warnings, and intentional concealment of risks.

September 10, 2025

• Rise in state court cases: New mesh lawsuits are being filed in New Jersey and Massachusetts, independent of the closed federal MDLs. State court cases often progress more quickly, allowing plaintiffs faster access to discovery, sooner trial schedules, and stronger negotiating power for potential settlements.

September 2, 2025

• UK study highlights risks: A five-year analysis of 785 women at a mesh specialist center revealed that the majority experienced chronic pain, more than half required mesh removal surgery, and many suffered recurrent stress urinary incontinence afterward.

September 1, 2025

• Expansion of mediation programs: Courts are increasing settlement opportunities for complex cases involving mesh erosion, multiple surgeries, and ongoing pelvic pain, while still permitting cases ready for trial to proceed.

June 19, 2025

• Ethicon Faces New Lawsuit in New Jersey: A recent state court case in New Jersey accuses Ethicon of causing lasting injuries from a pelvic mesh implant. The trial is set for July 21, 2025, with expert reports due by August 11 and discovery concluding on August 15. This case reflects the increasing number of individual state court filings against mesh manufacturers.

Transvaginal mesh implants were originally marketed as advanced treatments for pelvic organ prolapse (POP) and stress urinary incontinence (SUI). However, for many women, these devices resulted in serious harm rather than relief. The significant complications have prompted numerous lawsuits against leading manufacturers, as affected individuals pursue accountability for injuries that could have been avoided.

If you have suffered complications from a mesh implant, you might be eligible to participate in this legal action. Click HERE for a FREE case review.

Understanding Transvaginal Mesh

Transvaginal mesh (TVM) is a synthetic, net-like medical implant designed to provide support to weakened pelvic structures. It is surgically placed through the vaginal wall to reinforce muscles and organs that have lost strength. TVM was primarily used to address conditions such as:

• Pelvic Organ Prolapse (POP): A condition where organs like the bladder, uterus, or rectum descend from their usual position due to weakened pelvic muscles.
• Stress Urinary Incontinence (SUI): Involuntary urine leakage triggered by coughing, sneezing, laughing, or physical activity.

Regrettably, a significant number of these implants led to severe health issues, resulting in product recalls, FDA safety alerts, and numerous legal claims.

FDA Alerts and Oversight Measures

In 2008, the FDA released its first warning, noting that complications from transvaginal mesh were “not uncommon.” By 2011, the agency strengthened its warning, stating that such complications were not rare and could result in permanent, life-changing injuries.

In 2019, the FDA directed manufacturers to halt sales of transvaginal mesh for pelvic organ prolapse (POP) due to ongoing safety concerns. Despite this ban, thousands of women continue to suffer from pain and other complications caused by previously implanted devices.

Frequently Reported Transvaginal Mesh Complications

Litigation claims assert that transvaginal mesh has caused serious issues, including:

• Mesh erosion: Mesh cutting into vaginal walls or surrounding organs
• Chronic pelvic pain
• Painful sexual intercourse (dyspareunia)
• Bleeding and infections
• Bladder or bowel perforation
• Autoimmune or systemic reactions
• Multiple corrective surgeries
• Emotional distress and diminished quality of life

Many women have needed multiple revision surgeries but continue to experience persistent pain, discomfort, and functional limitations.

If you’ve experienced any of these complications after receiving a vaginal mesh implant, you may have a legal case. Click HERE for a FREE consultation with a partner attorney.

Companies and Mesh Products Involved in Legal Claims

The transvaginal mesh litigation includes claims against the following companies and their products:

Manufacturer	Devices
Ethicon (J&J)	Gynecare Prolift, Prosima, TVT, Gynemesh
Boston Scientific	Pinnacle, Obtryx, Advantage Fit, Solyx
C.R. Bard	Avaulta, PelviSoft, PelviLace
American Medical Systems (AMS)	MiniArc, Apogee, Perigee
Coloplast	Aris, Supris, Omnisure
Mentor	ObTape
Caldera Medical, Cook Medical, Tyco IVS	Various pelvic mesh products

Reasons Behind Transvaginal Mesh Lawsuits

These legal actions claim that mesh makers:

• Provided inaccurate or incomplete information to doctors and patients regarding the safety and performance of their implants
• Skipped thorough testing prior to releasing the products to the market
• Overlooked or minimized reports of adverse effects and complications
• Failed to give clear warnings about the potential risks associated with the devices

Consequently, numerous women experience long-term health issues, enduring chronic pain and lasting physical limitations.

What Types of Compensation May Be Available?

Individuals filing transvaginal mesh claims may pursue damages for:

• Medical expenses already incurred and anticipated future costs, including corrective surgeries
• Lost income and reduced earning capacity
• Physical pain and suffering
• Loss of spousal companionship or intimacy (loss of consortium)
• Emotional trauma and psychological distress
• Reduction in overall quality of life

Numerous cases have resulted in substantial monetary awards, including multimillion-dollar verdicts and settlements. In total, mesh manufacturers have paid out billions of dollars to resolve these legal claims.

What’s Driving the Rise in Lawsuits?

The increase in transvaginal mesh litigation is fueled by several key factors:

• Emerging studies highlighting long-term health risks
• FDA recalls and bans on certain mesh products
• Heightened patient awareness about the lack of prior warnings
• Continued reports of serious complications years after implantation

These cases go beyond seeking financial recovery—they aim to hold manufacturers responsible for prioritizing profits over the health and safety of patients.

What Steps Should You Take If Affected?

If you’ve had complications from a vaginal mesh implant, consider the following actions:

• Collect your medical records – Include surgical notes, hospital documents, and any records of corrective procedures.
• Keep detailed documentation – Track symptoms, pain, medical expenses, lost income, and other impacts.
• Speak with a qualified attorney – A lawyer experienced in product liability can evaluate your potential case.
• Move promptly – Statutes of limitations vary by state, so acting early helps preserve your right to file.

How ClaimsHotline.com Can Assist

ClaimsHotline.com helps women affected by transvaginal mesh implants connect with experienced attorneys handling cases across the country. Our legal partners provide a free evaluation to determine if you may qualify and guide you through your options at no cost.

If you or someone close to you has experienced health issues or injuries related to a vaginal mesh implant, click HERE to start your FREE case review today.