Transvaginal Mesh Settlements: What You Should Know

Published By:
Picture of Jessica Paluch-Hoerman
Jessica Paluch-Hoerman

Attorney Jessica Paluch-Hoerman, founder of TruLaw, has over 28 years of experience as a personal injury and mass tort attorney, and previously worked as an international tax attorney at Deloitte. Jessie collaborates with attorneys nationwide — enabling her to share reliable, up-to-date legal information with our readers.

This article has been written and reviewed for legal accuracy and clarity by the team of writers and legal experts at TruLaw and is as accurate as possible. This content should not be taken as legal advice from an attorney. If you would like to learn more about our owner and experienced injury lawyer, Jessie Paluch, you can do so here.

TruLaw does everything possible to make sure the information in this article is up to date and accurate. If you need specific legal advice about your case, contact us by using the chat on the bottom of this page. This article should not be taken as advice from an attorney.

Key takeaways:

  • Transvaginal mesh lawsuits stem from patients experiencing severe complications like pain, infection, and tissue erosion that significantly impact their quality of life, leading to substantial settlements from manufacturers.
  • Major manufacturers like Johnson & Johnson, Boston Scientific, and C.R. Bard have faced multimillion-dollar settlements for their transvaginal mesh products due to allegations of insufficient risk disclosure and deceptive marketing practices.
  • Individuals considering a transvaginal mesh lawsuit should consult with an experienced attorney who can evaluate their eligibility, gather necessary medical documentation, and navigate the complex legal process to seek just compensation for their injuries.

Overview of Transvaginal Mesh Settlements

On this page, we’ll discuss transvaginal mesh settlements, factors that may impact transvaginal mesh settlement amounts, how to maximize your compensation in a transvaginal mesh lawsuit, and much more.

Transvaginal Mesh Settlements What You Should Know

Intro to Transvaginal Mesh Settlements

Some of the key aspects of transvaginal mesh settlements include, but are not limited to:

  • Severity of Injuries: Settlement amounts often depend on the extent and severity of the plaintiff’s mesh-related complications and damages.
  • Medical Expenses: Compensation for past and future medical costs related to mesh complications is a significant component of many settlements.
  • Lost Wages and Earning Capacity: If mesh complications have impacted the plaintiff’s ability to work, settlements may include compensation for lost income and earning potential.
  • Pain and Suffering: Non-economic damages, such as pain, suffering, and loss of quality of life, are often factored into mesh lawsuit settlements.

If you’ve suffered complications from a transvaginal mesh implant, you may be eligible for significant compensation through a mesh lawsuit settlement.

Contact Tru Law using the chat on this page for a free case evaluation to learn more about the potential value of your transvaginal mesh claim and the settlement process.

Table of Contents

Transvaginal Mesh Lawsuit Updates Timeline

June 24th, 2025: Study Links Unique Bacteria on Mesh Implants to Chronic Pain and Complications in SUI Patients

Midurethral mesh slings, commonly used to treat stress urinary incontinence (SUI), have come under increasing legal and medical scrutiny due to serious complications reported by thousands of patients.

Complaints such as chronic pain, infections, mesh erosion, and organ perforation have led to growing concerns about the safety and design of these surgical implants.

New research published in the Applied and Environmental Microbiology journal in June 2025 offers fresh insight into the potential biological causes behind these issues.

The study found that the bacteria colonizing the mesh slings differ significantly from the typical microbial populations found in nearby vaginal, urinary, and skin environments.

In particular, mesh samples from patients with chronic pain showed greater bacterial diversity, including the presence of species such as Enterococcus—suggesting a connection between mesh-specific bacteria and inflammatory complications.

These findings support claims made in numerous lawsuits against mesh manufacturers.

Plaintiffs allege that the devices are defectively designed in a way that fosters harmful bacterial colonization and that companies failed to adequately warn patients or conduct sufficient premarket testing to uncover long-term health risks.

Legal actions seek compensation for a range of damages, including medical costs, lost wages, pain and suffering, and diminished quality of life.

As more scientific evidence emerges, the role of microbial colonization is becoming a key element in both understanding mesh complications and holding manufacturers accountable.

June 6th, 2025: Study Finds TVM Particles May Trigger Autoimmune Response, Raising New Legal Questions

A new study published in Nature Reviews Urology has found that microscopic particles from transvaginal mesh (TVM) implants may trigger autoimmune responses, even after the device has been surgically removed.

The research, led by Dr. Nicholas Farr, links residual polypropylene particles—commonly used in mesh products—to Autoimmune/Inflammatory Syndrome Induced by Adjuvants (ASIA).

According to the study, these particles can remain in surrounding tissue and provoke ongoing immune system activity, potentially worsening symptoms long after mesh removal.

These findings may impact current and future transvaginal mesh lawsuits by challenging earlier conclusions that dismissed any association between mesh implants and autoimmune disease.

In particular, the new evidence calls into question a 2017 study published in the American Journal of Obstetrics and Gynecology, which found no systemic health risks related to mesh use.

May 26th, 2025: FDA Proposes Reclassification of Transvaginal Mesh for POP as High-Risk

The U.S. Food and Drug Administration (FDA) announced a proposal to reclassify transvaginal mesh used for treating pelvic organ prolapse (POP) as a high-risk medical device.

If the proposal is finalized, manufacturers will be required to provide comprehensive data on the product’s safety and effectiveness before it can be marketed.

In addition to reclassifying the mesh itself, the FDA is also seeking to elevate the regulatory status of the surgical instruments used to implant and secure the mesh—from low-risk to moderate-risk—reflecting the growing concern over potential complications.

This move follows more than a decade of increasing scrutiny.

The FDA first flagged potential safety issues with vaginal mesh products in 2008 and later issued formal warnings and postmarket surveillance requirements in 2011 and 2012.

The proposed changes are now open for public comment for a 90-day period.

It’s important to note that these reclassifications apply only to mesh intended for vaginal POP repair and related tools; devices used for hernia repair, stress urinary incontinence, or abdominal POP procedures are not included in the proposal.

March 1st, 2025: Ongoing Developments in Transvaginal Mesh Litigation

Transvaginal mesh (TVM) implants were introduced in the late 1990s as a solution for pelvic organ prolapse (POP) and stress urinary incontinence (SUI).

Intended to reinforce weakened pelvic tissues, these devices quickly gained popularity—but over time, they became linked to serious and often debilitating complications, including chronic pelvic pain, organ perforation, bleeding, and mesh erosion.

These complications have triggered a wave of litigation against mesh manufacturers, as thousands of affected women have sought accountability and compensation.

Resolution of Federal MDLs: A Major Milestone

To manage the sheer volume of cases, many lawsuits were consolidated into multidistrict litigations (MDLs), streamlining the legal process while enabling more efficient case resolution.

The final federal MDL for transvaginal mesh concluded in November 2022, with numerous claims settled during the proceedings.

However, the end of the MDL does not prevent individuals from filing personal lawsuits.

Women who have experienced mesh-related injuries can still bring individual claims tailored to their specific circumstances.

Why Individual Claims Still Matter

Pursuing a separate lawsuit outside the MDL framework offers several potential advantages:

  • Customized Legal Strategy: Each case can be evaluated independently, allowing for personalized legal approaches and negotiation tactics.
  • Higher Compensation Potential: Individual cases are not bound by MDL settlement averages, which may lead to greater financial recovery based on the severity of the injuries.
  • Greater Plaintiff Control: Those pursuing individual claims often have more input over critical decisions, such as trial participation and settlement acceptance.

The Legal Landscape in 2025

Even with many high-profile settlements behind them, manufacturers continue to face litigation.

For example, Johnson & Johnson agreed to a $120 million settlement in January 2016 to resolve around 3,000 claims.

Yet, many lawsuits remain active, with both federal and state courts still handling unresolved cases.

Recent Global Developments

In August 2024, 140 women in the UK received compensation for injuries linked to vaginal mesh implants.

The claims targeted major manufacturers, including Johnson & Johnson, C.R. Bard, and Boston Scientific, and involved complications such as persistent pain, organ perforation, and mesh migration.

Women considering filing a lawsuit related to transvaginal mesh injuries should keep the following in mind:

  • Statute of Limitations: Deadlines for filing vary by state and country. Prompt legal consultation is crucial to avoid missing these time-sensitive windows.
  • Medical Documentation: Clear medical records linking the mesh implant to resulting health problems will strengthen a case.
  • Specialized Legal Support: Working with attorneys experienced in mesh litigation can significantly improve a claimant’s chance of success.

Despite the closure of the federal MDL, transvaginal mesh litigation remains active and evolving.

Women who continue to suffer from complications should explore their legal options, especially as new studies and settlements highlight the ongoing impact of these devices.

Let me know if you’d like this turned into a landing page, newsletter piece, or formatted infographic summary.

February 3rd, 2025: Oregon Jury Delivers Defense Verdict in Pelvic Mesh Malpractice Case

An Oregon jury has ruled in favor of the defense in a medical malpractice lawsuit involving the implantation of a pelvic mesh device.

The plaintiff accused urologist Dr. Michael Lemmers and the Legacy Health hospital system of negligence, alleging they failed to obtain proper informed consent before implanting the Boston Scientific “Uphold Lite” mesh device during a 2019 procedure to treat pelvic organ prolapse.

The case focused on claims that the patient was not adequately informed of the potential risks associated with the device.

Informed consent cases, particularly in the context of complex medical procedures, are notoriously difficult to win, and the jury’s decision reflects that legal reality.

New Mesh Lawsuits Continue Post-MDL Closure

Despite the formal closure of the vaginal mesh multidistrict litigation (MDL), new lawsuits are still being filed in state courts across the United States.

As of late 2024, legal efforts to hold mesh manufacturers accountable remain active, though outcomes have varied.

Internationally, the issue also persists.

In August 2024, more than 100 women in England received financial settlements for serious complications resulting from mesh implants.

Reported injuries included persistent pain, perforation of the bladder and bowel, bleeding, and mesh erosion through the vaginal wall.

While exact compensation amounts were not made public, the total reached into the millions of pounds.

Study Links Mesh Material to Rapid Degradation

Adding to the growing scrutiny, a recent study from the University of Sheffield in the UK has raised new concerns about the design and material quality of vaginal and pelvic mesh implants.

Researchers found that the plastic commonly used in these devices begins to degrade within just 60 days of implantation.

The study concluded that the material—widely believed to be biocompatible—may actually be prone to early breakdown, leading to inflammation, tissue damage, and long-term health complications.

These findings lend further support to ongoing claims that many mesh implants were fundamentally flawed in both design and manufacturing.

November 1st, 2024: Study Exposes Rapid Degradation of Polypropylene in Vaginal Mesh Implants

Groundbreaking research from the University of Sheffield has revealed significant flaws in the polypropylene (PP) material commonly used in transvaginal mesh (TVM) implants.

The study found that PP begins to degrade within just 60 days of being implanted, with further structural breakdown evident by 180 days.

This degradation, marked by oxidation and the buildup of polypropylene particles in nearby tissues, challenges long-held beliefs about the material’s chemical stability.

As the mesh deteriorates, it causes a growing disconnect between the implant and surrounding tissue, which can trigger inflammation, tissue damage, and chronic pain.

These findings call into question the overall biocompatibility of PP-based mesh devices, which have already been linked to serious complications such as pelvic pain, infections, and urinary problems.

The research adds scientific weight to the ongoing debate about the safety of these implants.

In response to mounting concerns, the NHS placed strict limitations on the use of TVM in 2018, allowing procedures only under a high-surveillance protocol.

The latest study further supports the claims of many women who have filed lawsuits after suffering long-term health issues from mesh implants.

In England alone, more than 100 cases have recently been resolved through settlements.

Advocates are now calling for urgent reforms and the development of safer, more sustainable materials to prevent further harm to patients undergoing treatment for pelvic organ prolapse and stress urinary incontinence.

October 20th, 2024: New Study Reveals Polypropylene Mesh Degrades Quickly, Raising Alarms Over Vaginal Implant Safety

Recent research has revealed that polypropylene—the primary material used in transvaginal mesh (TVM) implants—begins to break down within just 60 days of being implanted in the pelvic region.

This finding intensifies ongoing concerns about the long-term safety of TVM devices, which have been used to treat pelvic organ prolapse (POP) and stress urinary incontinence (SUI) but are linked to a range of serious complications.

Conducted by scientists at the University of Sheffield in the UK, the study used a sheep model, chosen for its anatomical similarities to the human pelvis.

Researchers discovered that polypropylene mesh became stiffer over time, exhibited signs of oxidation, and shed microscopic particles that were absorbed into the surrounding tissue—concentrations of which increased the longer the mesh remained implanted.

These results have sparked renewed calls from patient advocates and medical professionals for urgent reform.

Campaigners argue that the material was not sufficiently evaluated for pelvic use before being introduced into clinical practice.

Sheila MacNeil, an emeritus professor in biomaterials and tissue engineering, stressed the urgent need to develop safer alternatives to prevent further patient harm.

The study’s lead author, Dr. Nicholas Farr, expressed hope that the findings will encourage manufacturers to innovate and improve implant safety.

Meanwhile, Kath Sansom, founder of the patient advocacy group Sling The Mesh, cited the study as further proof of the dangers of polypropylene mesh and called for immediate changes in how pelvic conditions are treated.

This research follows a group settlement in which over 100 women in England received compensation after experiencing debilitating side effects from TVM implants.

Reported complications include chronic pelvic pain, infections, urinary difficulties, and the need for multiple revision surgeries.

The growing body of evidence has prompted medical and legal communities alike to push for stricter oversight, improved patient education, and the exploration of non-mesh alternatives for managing POP and SUI.

October 4th, 2024: Major Breakthrough in Hernia Mesh Lawsuit as Bard Reaches Settlement

The Bard Hernia Mesh multidistrict litigation (MDL) has taken a significant step forward, with a major settlement bringing relief to thousands of affected individuals.

C.R. Bard has agreed to resolve the vast majority of claims filed in both the federal MDL and Rhode Island state court, settling more than 30,000 cases related to injuries caused by its hernia mesh products.

This marks a major conclusion to a lengthy and challenging legal battle that has been ongoing since the MDL was established in August 2018.

The litigation experienced delays due to the COVID-19 pandemic and a series of complex trials across multiple jurisdictions.

A turning point came in early 2024, when the MDL judge paused a planned bellwether trial and ordered the parties into mediation.

Following months of negotiations, the parties have now reached an agreement to compensate victims who experienced complications from Bard’s allegedly defective hernia mesh devices.

The settlement represents a substantial victory for plaintiffs and moves the litigation closer to closure for thousands of injured patients.

June 20th, 2024: Appeals Court Upholds $2.5 Million Verdict in Vaginal Mesh Case Against Coloplast

The United States Court of Appeals for the Eleventh Circuit has affirmed a lower court ruling in the case of Virginia Redding v. Coloplast Corporation, a significant decision in the ongoing litigation over vaginal mesh implants.

The appeal focused on whether Redding’s product liability claim was filed within the statute of limitations under Florida law.

Redding filed her lawsuit on September 18, 2014, asserting that vaginal mesh devices manufactured by Coloplast were defectively designed and caused her serious injuries.

Coloplast contested the suit, arguing it was time-barred due to Florida’s four-year statute of limitations for product liability claims.

The company claimed Redding began experiencing symptoms more than four years before initiating legal action.

However, the appellate court agreed with the lower court’s finding that Redding was not aware—and had no reasonable way of knowing—before September 18, 2010, that her injuries were specifically linked to the mesh implants.

As a result, the court ruled that her claim was timely.

The jury in the original trial awarded Redding $2.5 million in damages.

Coloplast’s post-trial attempt to overturn the verdict through a renewed motion for judgment as a matter of law was also denied by the district court.

This decision underscores the legal challenges involved in product liability cases, particularly around the discovery of injury and the timing of legal claims.

It also marks another notable outcome in the broader landscape of vaginal mesh litigation.

May 1st, 2024: Philadelphia Jury Awards $20 Million in Vaginal Mesh Lawsuit Against Johnson & Johnson Subsidiary

A Philadelphia jury has awarded $20 million in damages to a woman from Cinnaminson, New Jersey, who suffered severe complications from a vaginal mesh implant manufactured by Ethicon, a division of Johnson & Johnson.

The verdict, reached in late April in the Philadelphia Court of Common Pleas, concluded a three-week trial centered on the safety and performance of the TVT-Secur transvaginal mesh device.

The woman had the mesh implanted to treat stress urinary incontinence, but within two months, the device began to erode.

Despite undergoing three separate surgeries in an attempt to remove the mesh, remnants of the device remain in her body, resulting in chronic pain and ongoing urinary issues.

Jurors determined that the device failed to perform as intended and that Ethicon failed to adequately warn healthcare providers and patients about the potential risks.

The jury awarded $2.5 million to cover medical expenses and other non-economic damages.

Additionally, $17.5 million in punitive damages was granted, signaling the jury’s conclusion that Ethicon’s conduct was grossly negligent.

The TVT-Secur device, which was used to address pelvic organ prolapse and urinary incontinence, has since been recalled. However, many patients who received this and other similar mesh products continue to face serious health complications.

This case adds to a growing list of high-value verdicts against Ethicon and Johnson & Johnson over their transvaginal mesh devices, which have been the subject of ongoing litigation due to their link to painful and often irreversible injuries.

April 11th, 2024: FDA Confirms SUI Mini-Slings Are as Safe and Effective as Traditional Mid-Urethral Slings

The U.S. Food and Drug Administration (FDA) has concluded its review of final reports from the mandated 522 postmarket surveillance studies on surgical mesh mini-slings used to treat stress urinary incontinence (SUI).

The findings indicate that SUI mini-slings perform as effectively as traditional mid-urethral slings over a 36-month period.

These studies revealed comparable rates and types of adverse events and re-surgery between mini-slings and traditional slings.

As part of its comprehensive evaluation, the FDA also conducted a systematic review of 30 randomized controlled trials published between 2013 and 2023.

This literature review further confirmed that mini-slings offer similar safety and efficacy outcomes when compared to conventional mid-urethral slings.

Surgical mesh slings remain a common treatment for SUI, and the FDA had previously required manufacturers to conduct long-term follow-up research specifically for mini-slings to assess their safety profile.

The newly released data reinforces confidence in the use of mini-slings as a viable option for managing SUI.

The FDA has stated it will continue to monitor these devices to ensure ongoing patient safety and optimal treatment outcomes.

March 12th, 2024: Vaginal Mesh Lawsuits Continue as Women Face Ongoing Health Struggles

The legal fight over vaginal mesh implants remains active, with many women still suffering from severe and lasting complications despite widespread awareness of the risks and a surge of lawsuits against manufacturers.

Originally intended to treat urinary incontinence and pelvic organ prolapse, transvaginal mesh implants have instead caused significant harm for countless women worldwide.

Commonly reported issues include chronic pain, mesh erosion into surrounding tissue, and worsening incontinence—often more severe than the original condition.

These complications frequently require multiple revision surgeries, yet complete relief is often out of reach.

Once implanted, the mesh is difficult to remove, and many patients are left dealing with persistent symptoms and long-term medical challenges.

The scale of harm has led to extensive litigation and large financial settlements.

Both healthcare providers and manufacturers now face mounting scrutiny over their role in promoting and utilizing these implants without fully disclosing the potential dangers.

Many women have successfully pursued legal action, bringing attention to the importance of informed consent and the need to consider non-surgical alternatives before proceeding with mesh procedures.

Still, too many patients continue to endure debilitating side effects, with little warning about the possible outcomes.

For those affected, the consequences are far-reaching.

Chronic pain, urinary issues, and the emotional burden of these conditions can significantly diminish quality of life, impacting everything from daily routines to long-term physical and mental well-being.

November 14th, 2023: Vaginal Mesh Lawsuit Continues as UK Settlement Highlights Ongoing Harm

The legal battle over vaginal mesh implants remains active, with recent developments underscoring the serious complications many patients have faced.

In the United Kingdom, a woman was awarded a £1 million settlement after enduring chronic pain and persistent health problems linked to a mesh implant procedure.

Vaginal mesh devices, commonly used to address urinary incontinence and pelvic organ prolapse, have been associated with a range of adverse effects.

Patients frequently report long-term pain, mesh erosion, and the recurrence of symptoms the implants were intended to resolve.

In numerous cases, surgeries were performed prematurely or without fully exploring less invasive alternatives, resulting in preventable harm.

These outcomes have prompted a wave of lawsuits, as individuals seek accountability and compensation for the physical, emotional, and financial toll they’ve endured.

For those affected by unnecessary or mishandled mesh surgeries, legal options may be available.

Compensation can help cover medical expenses, future care, lost income, and other damages.

The growing number of settlements emphasizes the critical need for informed consent and more cautious surgical decision-making.

If you’ve experienced complications from a vaginal mesh implant, you may be eligible to pursue a claim and receive the support you deserve.

October 17th, 2023: New Research Supports Safer Alternative to Traditional Vaginal Mesh Implants

Emerging scientific research is shedding light on safer materials for vaginal mesh implants, with promising findings favoring Polyvinylidene Fluoride (PVDF) over the commonly used polypropylene.

A 2023 study published in Diagnostics reports that PVDF meshes demonstrate greater biostability, trigger less inflammation, and result in reduced scarring—factors that significantly lower the risk of chronic pain following surgery.

In a three-year follow-up involving women treated for anterior or apical vaginal prolapse using PVDF meshes, 85.2% experienced successful anatomical outcomes, with few reports of complications like mesh exposure or discomfort.

Despite these advantages, PVDF meshes have yet to gain widespread use in the United States, primarily due to their higher cost compared to traditional polypropylene products.

Dr. Greg Vigna, a physician and legal advocate specializing in mid-urethral sling injuries, has voiced strong concerns about the continued reliance on polypropylene meshes in the U.S.

He urges the adoption of PVDF as a safer alternative and leads a legal team that represents women nationwide who have experienced complications from mesh implants.

June 22nd, 2023: Transvaginal Mesh Surgeries Under Scrutiny for Misinformation and Lasting Harm

Across the globe, countless women have undergone transvaginal mesh procedures without receiving full and accurate information about the risks involved—leading many to suffer severe, life-altering complications.

A recent review of transvaginal mesh case records uncovered alarming patterns in how these surgeries were communicated to patients.

The investigation, which analyzed over 40,000 pages of documentation from 18 women, revealed that poor communication and misleading consent practices left many unprepared for long-term outcomes such as chronic pain, nerve damage, and limited treatment options.

The findings exposed a troubling lack of transparency from medical professionals, resulting in widespread mistrust and inadequate post-operative care.

Many patients were not informed of alternative treatments or the potential for permanent complications.

The review called for the creation of a national registry to monitor mesh implant surgeries and removals, along with major improvements in patient aftercare, medical record-keeping, and physician-patient communication.

Widespread misinformation surrounding transvaginal mesh has caused significant physical and emotional damage.

As a result, legal challenges and public reviews continue to push for critical reforms in women’s healthcare and surgical accountability.

April 21st, 2023: Vaginal Mesh Implants Spark Legal Action and Demand for Better Care

Our Vaginal Mesh Lawyers are actively accepting clients. 

Initially introduced to treat stress urinary incontinence and pelvic organ prolapse following childbirth, vaginal mesh implants have led to widespread health complications, fueling a rise in lawsuits across the globe.

In Scotland alone, thousands of women underwent transvaginal mesh procedures before the practice was halted in 2018.

Many of these women have since reported debilitating side effects such as chronic pain, autoimmune responses, and extreme fatigue.

In many cases, the need for private treatment options has added emotional and financial strain.

To address the crisis, the Complex Mesh Surgical Service (CMSS) was created to assist affected patients.

However, numerous women have voiced frustrations with the system, citing unclear referral processes, delayed appointments, and limited awareness of mesh-related complications among general practitioners.

Some women even found themselves having to educate their own doctors about the risks and symptoms.

The severity of these complications has forced many individuals to leave their jobs and seek mesh removal surgeries—often traveling outside of Scotland for more specialized care.

As a result, a growing number of women are turning to the legal system in pursuit of justice through vaginal mesh lawsuits.

Advocates continue to call for better clinical guidance, quicker access to care, and more comprehensive treatment options to support those living with the long-term effects of mesh implants.

March 24th, 2023: Woman Sues J&J Over Vaginal Mesh Injuries Amid Global Legal Surge

TruLaw is now accepting vaginal mesh lawsuit clients.

Our legal team is currently representing individuals who have suffered complications from transvaginal mesh implants.

A recent case involves a 57-year-old woman from Canada who has initiated legal action against Johnson & Johnson, alleging severe health problems resulting from a surgical mesh device manufactured by its subsidiary, Ethicon.

The mesh was implanted in 2008 following a partial hysterectomy, and according to the complaint, it later caused chronic pain and internal organ damage.

For more than a decade, the plaintiff endured worsening symptoms that severely impacted her quality of life, including her ability to work and maintain personal relationships.

In 2021, medical evaluations revealed that the mesh had disintegrated and embedded itself into her organs.

This led to recurrent infections and required multiple surgeries—some of them emergency procedures—to prevent life-threatening sepsis.

Although Johnson & Johnson maintains that its pelvic mesh products are safe and effective, the company attributes its withdrawal from the market to business decisions, not safety concerns.

This position stands in contrast to mounting evidence and lawsuits worldwide that suggest serious risks linked to these devices.

Ethicon has already pulled several mesh products off the market—both for pelvic floor disorders and hernia repair—after reports surfaced of higher-than-expected failure rates and a significant number of revision surgeries.

These product removals have further intensified legal scrutiny and public criticism.

This new lawsuit, filed in Winnipeg, joins a growing wave of international litigation involving surgical mesh.

In countries such as Scotland, governments have begun offering support to affected women, including financial assistance for corrective mesh removal surgeries.

If you or a loved one has experienced complications from a transvaginal mesh implant, contact us today to explore your legal options.

January 1st, 2023: Vaginal Mesh Lawsuits Highlight Serious Health Risks and Legal Action

The ongoing vaginal mesh litigation centers around serious complications linked to transvaginal mesh implants, which were originally developed to treat pelvic organ prolapse (POP) and stress urinary incontinence (SUI).

Thousands of patients have come forward, claiming that these implants caused severe and often debilitating side effects. Reported complications include mesh erosion, infections, organ perforation, and painful intercourse.

Many individuals have required additional surgeries to correct these issues, and some continue to suffer from long-term pain and reduced quality of life.

Prominent medical device manufacturers facing legal challenges include Ethicon (a division of Johnson & Johnson), C.R. Bard, American Medical Systems, and others.

Plaintiffs argue that these companies failed to thoroughly test their products and did not adequately warn patients or healthcare providers about the potential for significant harm.

While many claims have been resolved through settlements, others remain active in court.

In response to growing scrutiny and accumulating evidence, some manufacturers have discontinued certain transvaginal mesh products altogether.

Notable Outcomes in Transvaginal Mesh Settlements

Transvaginal mesh is a medical device used to treat pelvic organ prolapse and stress urinary incontinence in women.

Transvaginal mesh cases have led to a series of lawsuits due to complications caused by the implant.

Notable Outcomes in Transvaginal Mesh Settlements

Entities like Johnson & Johnson and its subsidiary Ethicon, Inc., were involved in a mesh settlement in which they agreed to pay out millions due to deceptive marketing practices, as acknowledged by several Attorney Generals.

Notable outcomes in this area include:

Reasons for Filing Transvaginal Mesh Lawsuits

The reasons for filing vaginal mesh lawsuits often stem from patients experiencing adverse effects post-implantation, which they were not adequately warned about.

Notable Outcomes in Transvaginal Mesh Settlements; Reasons for Filing Transvaginal Mesh Lawsuits

Such effects can be life-altering and include severe pain, infection, tissue erosion, and urinary problems.

The largest transvaginal mesh settlements involve:

  • Claims for failing to disclose risks of the vaginal mesh device resulting in restitution to impacted individuals.
  • Legal actions against manufacturers for misrepresenting, insufficient instructions, and marketing of their transvaginal mesh devices, as seen in the action from Attorney General Bob Ferguson against Boston Scientific.

The patterns seen in these vaginal mesh case outcomes point to manufacturers bearing responsibility for their mesh device complications and marketing oversights, leading to significant financial and legal repercussions.

Complications from Transvaginal Mesh Implants

The introduction of transvaginal mesh implants brought about a significant evolution in the treatment of pelvic organ prolapse and stress urinary incontinence.

Notable Outcomes in Transvaginal Mesh Settlements; Reasons for Filing Transvaginal Mesh Lawsuits; Complications from Transvaginal Mesh Implants

However, a range of vaginal mesh complications that occurred with these surgical mesh devices have been documented, presenting varied challenges for affected women.

Common Issues Experienced by Women with Mesh Implants

Transvaginal mesh implants aim to provide structural support to weakened pelvic tissues, yet they can lead to multiple complications.

Below are some of the common issues that have emerged:

  • Mesh erosion, also known as mesh exposure, is a frequent complication where the mesh wears through the vaginal lining.
  • Women may suffer from chronic pain, which can be severe and interfere with daily activities.
  • Vaginal scarring and shrinkage from the mesh may lead to reduced vaginal functionality and painful intercourse.
  • There have been instances where vaginal mesh complications led to recurrent urinary tract infections due to irritation or injury.

Long-term Effects of Transvaginal Mesh Complications

Over time, transvaginal mesh complications can result in more persistent health issues that go beyond the immediate postoperative period.

Here are some long-term effects reported by women:

  • Long-term complications can include organ perforation, where the sharp edges of the mesh puncture adjacent organs.
  • Vaginal mesh injury may necessitate additional surgeries, sometimes requiring complete mesh removal.
  • Women may experience severe complications and injuries leading to a chronic condition that affects their quality of life.
  • Complications involving pelvic mesh have often required legal action, with numerous transvaginal mesh settlements reported.

Manufacturers Involved in Transvaginal Mesh Settlements

In the wake of numerous lawsuits, key manufacturers have faced settlements over the alleged harm caused by their transvaginal mesh products.

Notable Outcomes in Transvaginal Mesh Settlements; Reasons for Filing Transvaginal Mesh Lawsuits; Complications from Transvaginal Mesh Implants; Manufacturers Involved in Transvaginal Mesh Settlements

Major Companies Named in Mesh Lawsuits

Boston Scientific and Johnson & Johnson’s subsidiary Ethicon are among the major companies implicated in transvaginal mesh settlements.

They are just a portion of the larger group of vaginal mesh manufacturers that have been brought to court.

Here’s a breakdown of some of the settlements:

  • Johnson & Johnson: Faced a $116.9 million settlement due to misleading marketing practices related to the safety and effectiveness of its mesh devices.
  • Boston Scientific: Agreed to pay $188.6 million in a multistate settlement due to allegations of deceptive marketing.
  • C.R. Bard Inc.: Partook in a $60 million multistate settlement to resolve an investigation into its marketing practices.

Specific Products Linked to Transvaginal Mesh Settlements

Certain products stand out due to the volume of cases and the settlements reached in court.

Here are a few notable vaginal mesh products linked to legal actions:

  • Boston Scientific’s pelvic mesh products
  • Ethicon’s transvaginal surgical mesh devices
  • Products from American medical systems involved in litigation
  • Various devices by unnamed vaginal mesh makers that have been subject to court rulings

Compensation Amounts in Transvaginal Mesh Settlements

Recent transvaginal mesh settlements reflect these medical devices’ serious impacts on patients’ lives.

Notable Outcomes in Transvaginal Mesh Settlements; Reasons for Filing Transvaginal Mesh Lawsuits; Complications from Transvaginal Mesh Implants; Manufacturers Involved in Transvaginal Mesh Settlements; Compensation Amounts in Transvaginal Mesh Settlements

Compensations have been substantial, acknowledging the lasting harm caused by these products.

Range of Payouts Awarded in Mesh Lawsuits

The financial compensations in transvaginal mesh settlements vary significantly and have reached millions.

Here are key figures that have emerged from recent settlements:

  • The California Department of Justice announced a staggering settlement of $188.6 million as part of a multistate settlement.
  • Another high-profile pelvic mesh case resulted in a $116.9 million settlement with Johnson & Johnson and their subsidiary Ethicon, Inc.
  • A sum of $60 million was agreed upon in a multistate settlement with C.R. Bard Inc.
  • In Washington, a recovery effort allowed consumers to claim a share of a $9.9 million recovery.
  • Arizona received $2.8 million in penalties from Johnson & Johnson and Ethicon, Inc. as part of a larger national settlement.

Factors Influencing Transvaginal Mesh Settlement Amounts

Women who have suffered complications from transvaginal mesh implants may be entitled to compensation.

The amount of a settlement depends on the specific circumstances of each case.

Several factors affect the settlement amounts in transvaginal mesh cases:

  • Extent of Injury: The severity and permanence of the injuries are pivotal in determining settlement figures.
  • Impact on Quality of Life: How the mesh has affected a patient’s daily living and well-being influences compensation.
  • Employment: If the injury impacted the patient’s ability to work, settlements often reflect this economic loss.
  • Medical Expenses: The settlement calculation typically includes past and future medical costs associated with the injury.
  • Legal Precedents: Results of earlier vaginal mesh lawsuits often set benchmarks that influence new transvaginal mesh settlements.

These instances indicate that the legal system takes each mesh settlement case seriously, quantifying the harm inflicted upon patients and penalizing responsible entities accordingly.

Eligibility for Filing a Transvaginal Mesh Claim

Those seeking restitution through transvaginal mesh settlements must be aware of specific criteria to determine their eligibility to file a claim.

Notable Outcomes in Transvaginal Mesh Settlements; Reasons for Filing Transvaginal Mesh Lawsuits; Complications from Transvaginal Mesh Implants; Manufacturers Involved in Transvaginal Mesh Settlements; Compensation Amounts in Transvaginal Mesh Settlements; Eligibility for Filing a Transvaginal Mesh Claim

Adherence to these guidelines is essential for individuals to pursue compensation successfully.

Criteria for Pursuing a Mesh Settlement

If you received a transvaginal mesh implant to treat pelvic organ prolapse (POP) or stress urinary incontinence (SUI) and subsequently experienced complications, you may be eligible for compensation.

Here’s what you need to consider:

  1. The individual must have received a vaginal mesh implant for pelvic organ prolapse (POP) or stress urinary incontinence (SUI).
  2. Documentation or medical records must corroborate the surgical procedure and the mesh product used.
  3. Complications linked directly to the transvaginal mesh, such as pain, bleeding, or additional surgeries, should be evident.
  4. The filing must occur within the statute of limitations, which varies by state—knowledge of relevant deadlines from new vaginal mesh lawsuits is paramount.
  5. An association with existing vaginal mesh class actions or individual vaginal mesh lawsuits may influence eligibility.
  6. Prospective vaginal mesh plaintiffs should not have received compensation for the same claim previously.

Importance of Consulting with a Qualified Attorney

A qualified attorney plays a pivotal role in guiding both prospective and current vaginal mesh plaintiffs through the legal process.

Key reasons to seek legal counsel include:

  • An attorney can provide a detailed analysis of one’s case against the backdrop of recent woman’s vaginal mesh lawsuit settlements.
  • Legal expertise can ensure the right strategy is chosen, whether to join a vaginal mesh class action or file a new vaginal mesh lawsuit.
  • Lawyers can navigate the specifics of one’s medical situation and tie them to the vaginal mesh case parameters.
  • A seasoned legal professional can negotiate settlements and advocate for an individual’s rights and interests in court if necessary.

Engaging with an attorney with a clear track record in handling similar cases can be integral to achieving a favorable outcome.

Process of Filing a Transvaginal Mesh Lawsuit

When seeking justice for complications from transvaginal mesh, understanding the lawsuit process is essential.

Notable Outcomes in Transvaginal Mesh Settlements; Reasons for Filing Transvaginal Mesh Lawsuits; Complications from Transvaginal Mesh Implants; Manufacturers Involved in Transvaginal Mesh Settlements; Compensation Amounts in Transvaginal Mesh Settlements; Eligibility for Filing a Transvaginal Mesh Claim; Process of Filing a Transvaginal Mesh Lawsuit

This will set the stage for individuals to effectively pursue transvaginal mesh lawsuit settlements.

Steps Involved in Initiating a Mesh Claim

Filing a mesh lawsuit involves several key steps.

Here’s a look at what claimants need to know:

  1. Seek Legal Counsel: Individuals should consult with an attorney experienced in mesh lawsuits, who can evaluate the case.
  2. Medical Documentation: Gather thorough medical records linking injuries to the transvaginal mesh.
  3. Filing a Complaint: The attorney files a lawsuit in the correct jurisdiction.
  4. Multidistrict Litigation (MDL): Often, these claims are consolidated into an MDL, like the transvaginal mesh MDL in the Southern District of West Virginia.

Timeline for Reaching a Transvaginal Mesh Settlement

While some cases reach settlements quickly, others take significantly longer.

The path to a settlement can vary greatly, depending on both sides’ willingness to negotiate.

The path to a settlement can vary greatly, and these are some typical phases:

  • Discovery Process: Both sides exchange information and build their cases.
  • Pre-Trial Motions and Hearings: Courts may address legal challenges before trial.
  • Settlement Discussions: Negotiations might lead to a settlement before the case goes to trial.
  • Trial: If negotiations fail, the case goes to trial, which could take years.

Each vaginal mesh lawsuit follows its course, influenced by the United States Judicial Panel on Multidistrict Litigation and specifics of the case.

Success of Transvaginal Mesh Lawsuits to Date

The transvaginal mesh lawsuits have seen many cases filed, leading to substantial settlements for those affected by mesh-related complications.

Notable Outcomes in Transvaginal Mesh Settlements; Reasons for Filing Transvaginal Mesh Lawsuits; Complications from Transvaginal Mesh Implants; Manufacturers Involved in Transvaginal Mesh Settlements; Compensation Amounts in Transvaginal Mesh Settlements; Eligibility for Filing a Transvaginal Mesh Claim; Process of Filing a Transvaginal Mesh Lawsuit; Success of Transvaginal Mesh Lawsuits to Date

Number of Cases Filed Against Mesh Manufacturers

The battle in the courts against mesh manufacturers has been vigorous, with thousands of lawsuits filed across multiple states.

Here are some examples of legal action taken against mesh manufacturers:

  • California’s Department of Justice announced a substantial settlement, providing an example of the extensive legal actions taken.
  • A groundbreaking $344 million judgment by a California Superior Court against Johnson & Johnson for their surgical mesh products.
  • Further legal actions include rendering a multimillion-dollar verdict against the same company.
  • Many of these cases are grouped into larger, multi-state settlements, indicating widespread legal challenges for manufacturers.

Total Value of Transvaginal Mesh Settlements Reached

The settlements have provided financial compensation to many individuals affected by transvaginal mesh complications.

Key points on the settlements include:

  • One of the manufacturers, Boston Scientific, agreed with a coalition of 48 attorneys general.
  • Involved a $60 million agreement with C.R. Bard Inc. in September 2020.
  • Johnson & Johnson and Ethicon Inc. settled for $116.9 million with 41 states and the District of Columbia.
  • The total value of settlements reached across these various lawsuits reflects the severity of the allegations and underscores a pattern of accountability for the manufacturers involved.

Choosing the Right Transvaginal Mesh Lawyer

Selecting a transvaginal mesh lawyer is a significant step for those seeking justice for complications arising from surgical mesh intended to treat pelvic organ prolapse.

Notable Outcomes in Transvaginal Mesh Settlements; Reasons for Filing Transvaginal Mesh Lawsuits; Complications from Transvaginal Mesh Implants; Manufacturers Involved in Transvaginal Mesh Settlements; Compensation Amounts in Transvaginal Mesh Settlements; Eligibility for Filing a Transvaginal Mesh Claim; Process of Filing a Transvaginal Mesh Lawsuit; Success of Transvaginal Mesh Lawsuits to Date; Choosing the Right Transvaginal Mesh Lawyer

These legal professionals should not only be well-versed in the nuances of vaginal mesh lawsuits based on faulty medical devices. Still, they should also empathize with the physical and emotional distress caused by such surgical procedures.

Qualities to Look for in a Mesh Attorney

Finding the right legal representation after a complication from vaginal mesh is crucial.

You need an attorney with the experience and resources to navigate the complexities of these cases and fight for the compensation you deserve.

Notable Outcomes in Transvaginal Mesh Settlements; Reasons for Filing Transvaginal Mesh Lawsuits; Complications from Transvaginal Mesh Implants; Manufacturers Involved in Transvaginal Mesh Settlements; Compensation Amounts in Transvaginal Mesh Settlements; Eligibility for Filing a Transvaginal Mesh Claim; Process of Filing a Transvaginal Mesh Lawsuit; Success of Transvaginal Mesh Lawsuits to Date; Choosing the Right Transvaginal Mesh Lawyer; Qualities to Look for in a Mesh Attorney

When looking for a vaginal mesh lawyer, certain attributes stand out:

  1. Experience in handling mesh lawsuits shows proficiency in tackling specific challenges of such cases.
  2. A track record of successful settlements or verdicts indicating that the lawyer can effectively secure compensation for medical expenses and other damages.
  3. Resources to thoroughly investigate these complex cases, including access to medical experts and the latest legal precedents.
  4. Transparent communication, ensuring clients are kept informed throughout the process.

Benefits of Working with Experienced Transvaginal Mesh Lawyers

Facing complications from transvaginal mesh can be overwhelming.

Seasoned attorneys bring calmness to the storm by handling the legal battle, allowing you to focus on healing.

Notable Outcomes in Transvaginal Mesh Settlements; Reasons for Filing Transvaginal Mesh Lawsuits; Complications from Transvaginal Mesh Implants; Manufacturers Involved in Transvaginal Mesh Settlements; Compensation Amounts in Transvaginal Mesh Settlements; Eligibility for Filing a Transvaginal Mesh Claim; Process of Filing a Transvaginal Mesh Lawsuit; Success of Transvaginal Mesh Lawsuits to Date; Choosing the Right Transvaginal Mesh Lawyer; Qualities to Look for in a Mesh Attorney; Benefits of Working with Experienced Transvaginal Mesh Lawyers

Working with seasoned attorneys provides several advantages:

  • They understand the intricate details of medical device litigation, essential for building a strong case.
  • These lawyers are adept at articulating the extent of harm caused by a defective vaginal wall mesh, important for illustrating patient strife.
  • Experienced lawyers can strategically negotiate settlements for all incurred and future medical expenses.
  • They provide peace of mind, allowing individuals to focus on recovery while the legal aspects are handled with dexterity and care.

Transvaginal Mesh Lawsuit Frequently Asked Questions

Published By:
Picture of Jessica Paluch-Hoerman
Jessica Paluch-Hoerman

Managing Attorney & Owner

With over 25 years of legal experience, Jessica Paluch-Hoerman is an Illinois lawyer, a CPA, and a mother of three.  She spent the first decade of her career working as an international tax attorney at Deloitte.

In 2009, Jessie co-founded her own law firm with her husband – which has scaled to over 30 employees since its conception.

In 2016, Jessie founded TruLaw, which allows her to collaborate with attorneys and legal experts across the United States on a daily basis. This hypervaluable network of experts is what enables her to share the most reliable, accurate, and up-to-date legal information with our readers!

Additional Transvaginal Mesh Lawsuit resources on our website:
All
FAQs
Injuries & Conditions
Legal Help
Military
Other Resources
Settlements & Compensation
You can learn more about this topic by visiting any of our Transvaginal Mesh Lawsuit pages listed below:
#1 Transvaginal Mesh Attorney
Bladder Sling Lawsuit Statute of Limitations
Choosing the Right Transvaginal Mesh Lawyer
Common Vaginal Mesh Injuries Users Should Know
Common Vaginal Mesh Problems
Damages Linked to Vaginal Mesh Complications
Do I Qualify for a Vaginal Mesh Lawsuit?
FAQ: Are Transvaginal Mesh and Vaginal Mesh the Same?
FAQ: Do I Need A Transvaginal Mesh Attorney To File a Case?
FAQ: What Are Common Transvaginal Mesh Complications?
FAQ: What Do Transvaginal Mesh Attorneys Do for My Case?
FAQ: What Does A Vaginal Mesh Attorney Do For Your Lawsuit?
FAQ: What is the Purpose of a Transvaginal Mesh Implant?
FAQ: What is Trans Vaginal Mesh Used For?
FAQ: What is Transvaginal Mesh Used For?
FAQ: What is Transvaginal Mesh?
How Are Vaginal Mesh Problems or Complications Diagnosed?
How Can Transvaginal Mesh Complications Impact Quality Of Life?
How Common Are Vaginal Mesh Complications?
How Is Transvaginal Mesh Removal Performed?
How to Determine If You Have a Valid Vaginal Mesh Lawsuit?
How to File a Transvaginal Mesh Lawsuit?
How to Hire the Best Transvaginal Mesh Lawyer for Your Case
How To Seek Compensation In A Transvaginal Mesh Lawsuit
Long-term Impact of Transvaginal Mesh Complications
Statute of Limitations for Transvaginal Mesh Lawsuits
Transvaginal Mesh Alternatives
Transvaginal Mesh Class Action Lawsuits Explained
Transvaginal Mesh Implants: What You Need To Know
Transvaginal Mesh Lawsuit
Transvaginal Mesh Lawsuits: Settlement Amounts & Payouts
Transvaginal Mesh Revision Surgery: What to Expect
Transvaginal Mesh Settlements: What You Should Know
Types of Transvaginal Mesh
Vaginal Mesh Lawsuit Update | Vaginal Mesh Problems
Vaginal Mesh Lawsuits: Vaginal Mesh Surgery Injuries
Vaginal Mesh: What Can Be Used Instead of Mesh for Prolapse?
What Are The Challenges In Transvaginal Mesh Litigation?
What Are The Psychological Effects Of Transvaginal Mesh Surgery Complications?
What Are the Symptoms of Mesh Erosion?
What Are The Symptoms Of Transvaginal Mesh Complications?
What to Know When Hiring a Transvaginal Mesh Lawyer
What Women Should Know About Transvaginal Mesh
Why Do Some Transvaginal Mesh Implant Devices Fail?
Why Is Vaginal Mesh Surgery Controversial?
AFFF Lawsuit

AFFF Lawsuit claims are being filed against manufacturers of aqueous film-forming foam (AFFF), commonly used in firefighting.

Claims allege that companies such as 3M, DuPont, and Tyco Fire Products failed to adequately warn users about the potential dangers of AFFF exposure — including increased risks of various cancers and diseases.

Depo Provera Lawsuit

Depo Provera Lawsuit claims are being filed by individuals who allege they developed meningioma (a type of brain tumor) after receiving Depo-Provera birth control injections.

A 2024 study found that women using Depo-Provera for at least 1 year are five times more likely to develop meningioma brain tumors compared to those not using the drug.

Suboxone Lawsuit

Suboxone Tooth Decay Lawsuit claims are being filed against Indivior, the manufacturer of Suboxone, a medication used to treat opioid addiction.

Claims allege that Indivior failed to adequately warn users about the potential dangers of severe tooth decay and dental injuries associated with Suboxone’s sublingual film version.

Social Media Lawsuits

Social Media Harm Lawsuits are being filed against social media companies for allegedly causing mental health issues in children and teens.

Claims allege that companies like Meta, Google, ByteDance, and Snap designed addictive platforms that led to anxiety, depression, and other mental health issues without adequately warning users or parents.

Vaginal Mesh Lawsuits

Transvaginal Mesh Lawsuits are being filed against manufacturers of transvaginal mesh products used to treat pelvic organ prolapse (POP) and stress urinary incontinence (SUI).

Claims allege that companies like Ethicon, C.R. Bard, and Boston Scientific failed to adequately warn about potential dangers — including erosion, pain, and infection.

Bair Hugger Lawsuit

Bair Hugger Warming Blanket Lawsuits involve claims against 3M — alleging their surgical warming blankets caused severe infections and complications (particularly in hip and knee replacement surgeries).

Plaintiffs claim 3M failed to warn about potential risks — despite knowing about increased risk of deep joint infections since 2011.

Baby Formula NEC Lawsuit

Baby Formula NEC Lawsuit claims are being filed against manufacturers of cow’s milk-based baby formula products.

Claims allege that companies like Abbott Laboratories (Similac) and Mead Johnson & Company (Enfamil) failed to warn about the increased risk of necrotizing enterocolitis (NEC) in premature infants.

Do You
Have A Case?

Here, at TruLaw, we’re committed to helping victims get the justice they deserve.

Alongside our partner law firms, we have successfully collected over $3 Billion in verdicts and settlements on behalf of injured individuals.

Would you like our help?

Other Transvaginal Mesh Lawsuit Resources

All
FAQs
Injuries & Conditions
Legal Help
Military
Other Resources
Settlements & Compensation