How Are Vaginal Mesh Problems or Complications Diagnosed?

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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:

  • 1. Common transvaginal mesh complications include mesh erosion (where mesh pokes through the vaginal wall), pelvic pain, painful intercourse, irregular bleeding, and urinary problems such as incontinence, infection, and retention.
  • 2. The FDA has issued warnings about transvaginal mesh for pelvic organ prolapse due to complications, with mesh erosion being the most frequently reported issue, leading many patients to require additional surgical interventions.
  • 3. Studies indicate that bacterial colonization may contribute to mesh-related complications, and patients experiencing symptoms should seek evaluation from specialists who can provide appropriate management options.

FAQ: How Are Transvaginal Mesh Problems Diagnosed?

Question: How are Transvaginal Mesh Problems Diagnosed?

Answer: Transvaginal mesh problems are diagnosed through a combination of patient symptom evaluation, physical examination, and advanced diagnostic testing, including pelvic ultrasounds, MRIs, and cystoscopy, with healthcare providers examining for signs of mesh erosion, exposure, infection, and organ perforation.

On this page, we’ll answer this question in further depth, covering diagnostic procedures for transvaginal mesh complications, warning signs of mesh erosion and exposure, and the connection between properly diagnosed mesh injuries and transvaginal mesh lawsuits.

How Are Transvaginal Mesh Problems Or Complications Diagnosed; How Are Transvaginal Mesh Problems Or Complications Diagnosed; Managing Transvaginal Mesh Problems

Transvaginal Mesh Lawyers Helping Women With Diagnosed Complications

Attorneys nationwide continue pursuing compensation for women who have received medical diagnoses confirming transvaginal mesh complications, including mesh erosion, organ perforation, chronic infection, and recurrent urinary problems.

Thousands of women have undergone diagnostic procedures revealing serious mesh-related injuries that manufacturers allegedly knew about but failed to adequately warn patients or doctors about these risks.

Common diagnostic findings in mesh lawsuits include:

  • Mesh erosion: Physical examination and imaging revealing mesh protruding through vaginal tissue
  • Organ damage: Cystoscopy or other specialized tests showing mesh perforating the bladder or other organs
  • Chronic infection: Laboratory tests confirming persistent infections at the mesh implant site
  • Nerve damage: Neurological assessments confirming pain and nerve impairment related to mesh placement

TruLaw is currently accepting clients seeking compensation for medical expenses, lost wages, pain and suffering, loss of quality of life, and the emotional trauma associated with these complications.

If you’ve been diagnosed with transvaginal mesh complications, you may be eligible to seek compensation through a lawsuit.

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

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.

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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.

How Can A Transvaginal Mesh Attorney from TruLaw Help You?

Our Transvaginal Mesh attorney at TruLaw is dedicated to supporting clients through the process of filing a transvaginal mesh lawsuit.

With extensive experience in product liability cases, Jessica Paluch-Hoerman works with litigation leaders and medical experts to prove how defective mesh devices cause patient harm.

TruLaw focuses on securing compensation for medical expenses, lost income, and pain and suffering from manufacturers who knew about problems but continued selling dangerous products.

We understand the physical and emotional toll that transvaginal mesh complications have on your life and provide the personalized guidance you need when seeking justice.

Meet the Lead Transvaginal Mesh Attorney at TruLaw

Meet our lead Transvaginal Mesh attorney:

  • Jessica Paluch-Hoerman: As founder and managing attorney of TruLaw, Jessica brings her experience in product liability and personal injury to her client-centered approach by prioritizing open communication and personalized attention with her clients. Through TruLaw and partner law firms, Jessica has helped collect over $3 billion dollars on behalf of injured individuals across all 50 states through a variety of 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 allows us to focus 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: Consult with leading medical experts to support your case and demonstrate how mesh products caused your injuries.
  • 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 instant case evaluation process simplifies the legal process of qualifying and filing your claim, providing you with the knowledge and confidence needed to make informed decisions about your case.

If you or a loved one experienced complications from transvaginal mesh implants, 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.

Diagnostic Methods Used by Health Care Providers

Healthcare providers use various diagnostic approaches to identify transvaginal mesh complications, from initial assessments to advanced imaging techniques.

The evaluation process typically begins with a thorough patient history and physical examination, followed by specialized imaging when needed to confirm the diagnosis and determine the extent of mesh-related issues.

Initial Assessment of Transvaginal Mesh Problems

The first step in diagnosing transvaginal mesh problems involves a detailed patient history and symptom evaluation.

Women experiencing complications often report pelvic pain, vaginal discharge, bleeding, painful intercourse (dyspareunia), and urinary symptoms.

These symptoms may develop immediately after mesh placement or years later.

During the physical examination, healthcare providers perform a thorough vaginal examination to identify:

  • Mesh exposure or erosion through the vaginal wall
  • Areas of tenderness or pain when applying pressure to specific vaginal regions
  • Trigger points that produce pain when the mesh is palpated
  • Changes in vaginal tissue quality, including scarring or contraction
  • Pelvic floor muscle tension or spasms

This initial assessment helps determine whether symptoms are related to mesh complications and guides decisions about further diagnostic testing.

If symptoms persist or the examination reveals signs of mesh-related problems, healthcare providers may recommend advanced imaging to fully evaluate the condition.

Advanced Imaging to Detect Mesh Implant Issues

When physical examination findings suggest transvaginal mesh complications, healthcare providers may use several advanced imaging techniques to confirm the diagnosis and plan appropriate treatment:

  • Transvaginal Ultrasound (TVUS): This non-invasive first-line imaging method offers real-time visualization of mesh position, surrounding tissues, and complications without radiation exposure while guiding treatment planning for mesh removal procedures.
  • Endovaginal Ultrasound (EVUS): Endovaginal ultrasound provides enhanced visualization of mesh placement and integration to determine the full extent of mesh-related issues and assist surgeons in planning partial or complete mesh removal.
  • Magnetic Resonance Imaging (MRI): MRI delivers detailed images of pelvic organs, soft tissues, inflammatory changes, and potential mesh erosion into surrounding structures when ultrasound results are inconclusive or additional information is needed for surgical planning.
  • Cystoscopy and Proctoscopy: These endoscopic procedures enable direct visualization of the bladder and rectum to identify mesh erosion, assess tissue damage, and guide surgical planning for mesh removal and repair.

The combination of physical examination findings and advanced imaging results enables healthcare providers to make accurate diagnoses and develop personalized treatment plans for women experiencing transvaginal mesh complications.

If you have concerns about potential mesh-related symptoms, contact TruLaw using the chat on this page to receive an instant case evaluation that can determine your eligibility to join others in filing a transvaginal mesh lawsuit.

Physical Examination for Mesh Sling Complications

Healthcare providers use specific examination techniques to assess the presence of mesh-related issues and determine appropriate treatment options.

Women experiencing symptoms after mesh surgery should seek medical evaluation by providers with experience in recognizing mesh complications.

Evaluating Pain and Discomfort After Mesh Surgery

Pain is among the most common complications following transvaginal mesh surgery, often described as pelvic pain, vaginal pain, or pain during sexual intercourse (dyspareunia).

Pain following mesh placement requires methodical evaluation to distinguish between various potential causes and determine the most appropriate treatment approach:

  • Focused Pelvic Examination: Healthcare providers perform a systematic assessment of the pelvic skeletal and muscular anatomy to identify specific sources of mesh-related pain.
  • Levator Ani Assessment: This evaluation examines muscle tone and tenderness in the pelvic floor, which frequently contributes to postoperative pain following mesh procedures.
  • Bimanual Examination: Clinicians gently manipulate pelvic organs to evaluate pain responses that may indicate mesh adherence to surrounding structures or inflammation.
  • Cotton Swab Test: This diagnostic technique maps pain distribution along vaginal walls by applying gentle pressure with a cotton-tipped applicator to identify specific painful regions related to mesh placement.
  • Mesh Palpation: Practitioners apply precise pressure along the path of the mesh sling to locate trigger points that reproduce the patient’s typical pain symptoms.
  • Nerve Pathway Assessment: This evaluation focuses on pudendal and obturator nerve routes to identify nerve compression or irritation that may be causing neuropathic pain following mesh placement.

Pain after surgical treatment may be immediate or develop years after the procedure.

The pattern, timing, and intensity of pain provide valuable diagnostic information.

Persistent pain following a mesh sling surgical procedure often requires evaluation by healthcare providers familiar with mesh complications.

Identifying Signs of Transvaginal Mesh Exposure

Mesh exposure or erosion occurs when the mesh material becomes visible through vaginal tissue or protrudes into surrounding organs.

Diagnosing mesh complications begins with careful visual inspection, which allows clinicians to identify exposure or erosion that may require intervention:

  • Speculum Examination: Clinicians conduct a detailed vaginal examination using a speculum to thoroughly visualize all vaginal walls for signs of mesh complications.
  • Mesh Exposure Assessment: Healthcare providers look for areas where mesh is visible through the vaginal epithelium, which may appear as small openings with visible mesh material, red granulation tissue surrounding exposed mesh, abnormal discharge, or vaginal wall thinning.
  • Pain Response Evaluation: Practitioners assess for tenderness or pain when touching exposed mesh areas to determine sensitivity and help gauge the extent of inflammation or nerve involvement.
  • Urethral Inspection: This focused examination evaluates the urethra and areas around the bladder neck for signs of mesh erosion causing urinary symptoms and predisposing patients to recurrent infections.
  • Mesh Contraction Analysis: Clinicians evaluate for mesh contraction, which may cause puckering or tightening of vaginal tissue leading to pain, dyspareunia, and reduced vaginal caliber.

Mesh exposure can cause symptoms including vaginal discharge, spotting or bleeding, pain during sexual intercourse, and recurrent urinary tract infections.

In some cases, mesh exposure may be present without obvious symptoms, making regular follow-up examinations important after mesh placement.

If physical examination reveals signs of mesh complications, healthcare providers may recommend additional diagnostic tests, including imaging studies, to fully assess the extent of the problem and develop a treatment plan.

If you’ve been diagnosed with mesh exposure or erosion following transvaginal mesh surgery, contact TruLaw using the chat on this page to receive an instant case evaluation that can determine your eligibility to seek compensation for medical expenses and other damages.

Female Pelvic Reconstructive Surgery Evaluation

Pelvic reconstructive surgery addresses structural abnormalities that develop when a woman’s pelvic floor tissues weaken or tear.

This comprehensive evaluation typically begins with a detailed patient history and systematic pelvic examination that assesses the type and degree of support defects present.

For patients experiencing pelvic organ prolapse, an examination using the Pelvic Organ Prolapse Quantification System (POP-Q) helps determine the severity of displacement, with measurements taken at specific vaginal points to document the precise anatomical changes and stage the condition from 0-4.

Women with stress urinary incontinence undergo specialized testing including urodynamic studies that measure bladder pressure, urine flow rates, and sphincter function during various activities to assess the extent of urethral hypermobility or intrinsic sphincter deficiency.

Prior to considering transvaginal mesh placement—a surgical technique that has faced scrutiny from regulatory agencies—patients require thorough counseling about alternative treatment options including non-surgical approaches and native tissue repairs without synthetic materials.

Determining the Need for Corrective Mesh Surgery

Surgical mesh placement may be considered in specific cases of advanced pelvic organ prolapse (stages 3-4) where native tissue repairs have previously failed or when patients have risk factors for recurrence such as chronic high intra-abdominal pressure or connective tissue disorders.

Since the FDA’s 2019 order removing transvaginal mesh products for prolapse from the market, abdominal approaches using mesh (like sacrocolpopexy) have become the preferred surgical option when mesh reinforcement is deemed necessary, with studies showing success rates up to 90% for long-term anatomical support.

The decision-making process must include a personalized risk-benefit analysis, as mesh-related complications including erosion, pain, infection, and organ perforation can impact the quality of life and often require additional surgical interventions for correction.

Physicians must document that patients fully understand that while mesh may provide superior anatomical support in certain cases, it carries unique risks that non-mesh procedures do not and that some mesh-related complications can be permanent despite surgical correction attempts.

Pre-operative Assessment of Mesh Complications

For women who have previously undergone mesh procedures and are experiencing complications, evaluation begins with a focused history detailing symptom onset, progression, and specific triggers for urinary symptoms, pain, or vaginal discharge.

A thorough pelvic examination may reveal mesh erosion (exposure through vaginal tissue), palpable bands causing pain or dyspareunia, or signs of infection, while specialized tests including cystoscopy or proctoscopy may be needed to diagnose mesh penetration into adjacent organs.

Women with pelvic floor disorders frequently experience overlapping conditions, requiring careful differentiation between mesh-related symptoms and other conditions like overactive bladder, interstitial cystitis, or myofascial pain that may coexist or mimic mesh complications.

Imaging studies including pelvic ultrasound, MRI, or CT scans with specific mesh protocols help visualize the exact location of mesh implants and their relationship to surrounding structures.

TruLaw: Your Vaginal Mesh Injuries Law Firm

Vaginal mesh lawsuits are being filed by individuals across the country who were injured by defective vaginal mesh implants.

TruLaw is currently accepting clients for the vaginal mesh injury lawsuits.

A few reasons to choose TruLaw for your vaginal mesh injury case include:

  • If We Don’t Win, You Don’t Pay: The vaginal mesh injury lawyers at TruLaw and our partner firms operate on a contingency fee basis, meaning we only get paid if you win.
  • Expertise: We have years of experience handling medical device cases similar to vaginal mesh injury lawsuits, which helps us anticipate what we can expect to see in your case and the regulations we will be required to meet.
  • Successful Track Record: TruLaw and our partner law firms have helped our clients recover billions of dollars in compensation through verdicts and negotiated settlements.

If you or a loved one suffered injuries from a defective vaginal mesh implant, you may be eligible to seek compensation.

Contact TruLaw using the chat on this page to receive an instant case evaluation that can determine if you qualify for the vaginal mesh injury lawsuits today.

Transvaginal Mesh Lawsuit Frequently Asked Questions

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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!

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You can learn more about this topic by visiting any of our Transvaginal Mesh Lawsuit pages listed below:
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Common Vaginal Mesh Injuries Users Should Know
Common Vaginal Mesh Problems
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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?
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How to File a Transvaginal Mesh Lawsuit?
How to Hire the Best Transvaginal Mesh Lawyer for Your Case
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Long-term Impact of Transvaginal Mesh Complications
Statute of Limitations for Transvaginal Mesh Lawsuits
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