FAQ: What Do Transvaginal Mesh Attorneys Do for My Case?

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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:

  • TruLaw's Transvaginal Mesh Attorneys help clients who suffer from mesh implant complications. They guide you through the lawsuit process, collect needed medical records and negotiate for fair compensation.
  • Transvaginal mesh implants are used to treat conditions like stress urinary incontinence or pelvic organ prolapse. But, they can cause health issues such as pain during normal activities, tissue erosion and organ perforation.
  • If you've had complications after a transvaginal mesh surgery, you might have a medical defect case. Contact an attorney quickly as there are time limits on filing cases.
  • Choosing the right law firm is critical - look for those with experience in similar lawsuits like TruLaw which has won 99% of its cases. They offer free consultations without any obligation!

What Do Transvaginal Mesh Attorneys Do for My Case? Lets Discuss.

Question: What do Transvaginal Mesh Attorneys do for my case?

Answer: Transvaginal Mesh Attorneys can provide specialized legal assistance to individuals have experienced complications or adverse effects due to transvaginal mesh or a surgical mesh procedure.

Overview of Transvaginal Mesh Attorneys

The responsibilities of Transvaginal Mesh Attorneys at TruLaw include, but are not limited to:

  • Case Evaluation;
  • Gathering Evidence;
  • Negotiating Settlements;
  • Litigation;
  • Financial Compensation;
  • Specialized Knowledge;
  • and much more.

FAQ What Do Transvaginal Mesh Attorneys Do for My Case; Transvaginal Mesh Attorneys Understanding Transvaginal Mesh; Seeking Legal Help From Transvaginal Mesh Attorneys; Choosing the Right Transvaginal Mesh Attorneys; What to Expect Transvaginal Mesh Attorneys; Common Questions about Transvaginal Mesh Attorneys and Lawsuits

Are you struggling with complications from a transvaginal mesh implant?

This is a recognized problem affecting many women, resulting in distress and significant health issues.

On this page, we’ll discover what a transvaginal mesh attorney can do for your case – by providing an overview from initial consultation to possible settlement or trial proceedings.

If you’ve experienced vaginal mesh complications, injuries, or adverse effects from a transvaginal mesh implant- you may be eligible to file for the Transvaginal Mesh Lawsuit.

Contact the experienced Transvaginal Mesh Attorneys at TruLaw today for a no-obligation consultation.

We’re here to help you seek the compensation you deserve.

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.

Transvaginal Mesh Attorneys: Understanding Transvaginal Mesh

This section delves into the details of transvaginal mesh implants, discussing what they are, their safety considerations, and potential complications that may arise from their use.

Transvaginal Mesh Attorneys Understanding Transvaginal Mesh

What is Transvaginal Mesh?

Transvaginal mesh is a net-like implant made of synthetic material that doctors use in surgical procedures to treat conditions such as stress urinary incontinence (SUI) and pelvic organ prolapse (POP).

Surgeons insert it through the vaginal wall, providing support to weakened or damaged tissues.

Transvaginal mesh procedures can sometimes be referred to as tape, sling, ribbon, surgical mesh devices, or pelvic mesh.

Its primary function is to hold up pelvic organs, like the bladder or uterus, that have slipped out of place due to childbirth, surgery, or age.

Are Transvaginal Mesh Implants Safe?

The safety of transvaginal mesh implants has sparked much debate. The U.S. Food and Drug Administration (FDA) has classified complications from these devices as “not rare.”

This perspective contrasts significantly with the initial perception of these medical products, which doctors viewed as a revolutionary treatment for conditions such as pelvic organ prolapse.

Numerous adverse reports have surfaced over time, placing the safety of these implants under intense scrutiny.

One common complication is vaginal tissue erosion, making abdominal surgeries using similar mesh materials a safer alternative.

Chronic pelvic pain also plagues many patients who have undergone procedures involving transvaginal mesh implants.

As a result of excruciating pain, professionals are feverishly seeking other therapeutic solutions to address health concerns previously treated with this controversial device.

Vaginal Mesh Complications

Mesh implants are not without their own set of risks.

The complications can vary in severity and frequency, but some are common across most patients.

More often than not, women with transvaginal mesh implants report pain during intercourse or while going about normal activities.

In rare but serious cases, the mesh can actually erode the vaginal tissue leading to infection and other health issues such as vaginal scarring.

Another potential complication is organ perforation where the sharp edges of the mesh cut into organs surrounding tissue, like bladder, bowel or blood vessels around it.

Bleeding caused by such perforations could lead to severe consequences if left untreated.

Other reports include recurrent pelvic organ prolapse (where organs fall down or slip out of place) and urinary problems following the transvaginal repair surgery.

Transvaginal Mesh Attorneys navigate these complexities to file lawsuits alleging such medical deficiencies for their clients.

Seeking Legal Help From Transvaginal Mesh Attorneys

If you’ve ever suffered serious complications or complications from a transvaginal mesh implant, it’s important to seek qualified legal help to assess your medical defect case and understand how an experienced transvaginal mesh defect lawyer can aid in your pursuit for justice.

Transvaginal Mesh Attorneys Understanding Transvaginal Mesh; Seeking Legal Help From Transvaginal Mesh Attorneys

Do I Have a Medical Defect Case?

In the event that you’ve experienced complications like pain, bleeding, or organ perforation after a transvaginal mesh surgery, you may indeed have a medical defect case.

It’s important to note that anyone who has suffered infections, recurring incontinence, or other side effects due to faulty surgical mesh should seek legal advice immediately.

Typically, women suffering from pelvic organ prolapse repair complications triggered by transvaginal mesh implants can hold manufacturers accountable through lawsuits.

The law places time restrictions on such cases; hence knowing your statute of limitations for filing a bladder sling lawsuit is crucial.

Transvaginal Mesh Attorneys are experts at these matters and can assist effectively in determining if you have a viable medical defect case against the manufacturer based on your particular circumstances.

How a Transvaginal Mesh Lawyer Can Help

A Transvaginal Mesh Defect Lawyer provides vital support for people facing complications from mesh implants.

They guide clients through each step of the legal process, ensuring their rights are protected.

With in-depth knowledge about transvaginal meshes and associated cases, these attorneys develop a strong lawsuit against the responsible parties.

The lawyer collects necessary medical records, communicates with doctors to understand the severity of injuries and establishes a link between implant complications and your suffering.

They also negotiate with insurance companies or defendants for fair compensation to cover costs like medical bills, lost wages due to time off work, emotional distress, and pain suffered.

Furthermore, they have access to expert witnesses who can help strengthen your case if it goes to trial.

Choosing the Right Transvaginal Mesh Attorneys

Selecting the right transvaginal mesh attorney is critical to the success of your case, as they should have a proven track record in handling similar lawsuits and be able to provide personalized representation.

Transvaginal Mesh Attorneys Understanding Transvaginal Mesh; Seeking Legal Help From Transvaginal Mesh Attorneys; Choosing the Right Transvaginal Mesh Attorneys

TruLaw’s Experienced Legal Representation

TruLaw stands as a beacon for individuals impacted by transvaginal mesh complications.

With a proven track record of winning 99% of cases, the firm’s success speaks volumes about its capabilities and commitment.

The team at TruLaw consists predominantly of women, ensuring compassionate understanding paired with aggressive legal strategies.

Their experienced transvaginal mesh attorneys work diligently to ensure that each client is not just another case number, but a person deserving justice.

Why Choose TruLaw?

Selecting TruLaw as your legal representative in a transvaginal mesh case can lead to empowered and confident decisions.

With their specialized insight into such cases, they ensure that you receive proper guidance throughout the intricate legal process.

A key strength of TruLaw lies in holding manufacturers accountable for harm caused due to their products, driven by their belief in justice for those affected.

The firm boasts an impressive success rate of 99% in dealing with transvaginal mesh cases – an essential fact that underscores their prowess and dedication.

An added bonus? You get all this expert advice during a free consultation with no obligation attached!

These results confirm TruLaw’s commitment to fighting on behalf of the women affected by the complications of transvaginal mesh implants.

What to Expect: Transvaginal Mesh Attorneys

At the initial consultation, our experienced transvaginal mesh attorneys take the time to understand your situation thoroughly.

Transvaginal Mesh Attorneys Understanding Transvaginal Mesh; Seeking Legal Help From Transvaginal Mesh Attorneys; Choosing the Right Transvaginal Mesh Attorneys; What to Expect Transvaginal Mesh Attorneys

Initial Consultation and Evaluation

This involves listening to your story, reviewing relevant medical records and evaluating if there are solid grounds for a lawsuit.

A complete investigation helps us determine how best to proceed with your case.

We focus on identifying any complications or harm caused by a defective transvaginal mesh implant you might have received.

The discussion is confidential and comes at no cost to you since we believe in supporting those affected through their legal journey from day one.

Filing a Lawsuit

After an in-depth evaluation of your case, the attorney proceeds to file a lawsuit on your behalf.

This vital step involves drafting and submitting a formal complaint against the parties responsible for your severe pain and complications arising from the Transvaginal Mesh implant.

It’s crucial to note that filing a lawsuit doesn’t always mean going into full-scale court proceedings; many cases get resolved through settlements before reaching trial stage.

The mission at this juncture becomes ensuring you secure the maximum compensation for all distress endured as one of the thousands who have had their lives painfully disrupted by defective transvaginal mesh implants.

Your lawyer will handle all legal aspects, allowing you to focus much-needed energy on healing and recovery.

Negotiating a Settlement

Negotiation is a crucial phase in the lawsuit process.

Your attorney’s skill during this stage can substantially influence the compensation you receive for your transvaginal mesh injury claim.

They engage with manufacturers, presenting compelling evidence about how the defective device directly caused your suffering and expenses.

Strategies employed by attorneys often involve citing possible jury awards based on previous settlements.

The goal is to convince manufacturers that settling the case would cost them less than going to trial where they might face considerable damages.

As an example, one of the most substantial transvaginal mesh settlements reached extends into billions – proof that juries empathize with victims’ plights and are willing to require manufacturers to pay hefty compensations.

Going to Trial

Transvaginal mesh lawsuits that proceed to trial involve a detailed presentation of evidence before a jury.

Witnesses are called, medical records examined and experts testify in order to shed light on the complexity of each unique case.

The jury examines factors such as the severity of complications and financial losses due to surgeries or treatments required as part of their decision-making process.

Ultimately, they determine liability and assess potential damages awarded to the plaintiff based on this information.

Common Questions about Transvaginal Mesh Attorneys and Lawsuits

This section will delve into the frequently asked questions surrounding transvaginal mesh lawsuits, addressing concerns about the potential success rate of these cases, the process for determining if you might have a valid claim, and offering insight into how case value is calculated.

Transvaginal Mesh Attorneys Understanding Transvaginal Mesh; Seeking Legal Help From Transvaginal Mesh Attorneys; Choosing the Right Transvaginal Mesh Attorneys; What to Expect Transvaginal Mesh Attorneys; Common Questions about Transvaginal Mesh Attorneys and Lawsuits

What are My Chances of Winning a Lawsuit?

In assessing your likelihood of winning a lawsuit, several factors come into play.

Each case is unique; the specifics of your situation dictate the outcome.

The severity of complications from your transvaginal mesh implant, relevant medical reports, and how significantly this has affected your life are all carefully reviewed.

Yet, history leans favorably towards victims in these lawsuits.

Do I Have a Case?

Several factors determine whether you can pursue a transvaginal mesh lawsuit.

You may have a legal case if you suffered adverse effects after having a transvaginal mesh implant, especially complications like pain, bleeding, organ perforation or reoccurrence of pelvic organ prolapse.

A vital piece to build your case is evidence that connects your health issues directly to the implanted device.

Also, important is proving that the manufacturer failed in its duty to ensure the product’s safety or adequately warn about potential risks.

With these elements and guidance of an experienced attorney, your chance for successfully pressing charges significantly explores upwards.

What is the Value of My Case?

Determining the value of your transvaginal mesh case involves several factors.

Severity and persistence of injuries, the impact on quality of life, medical expenses, lost wages, and potential future care needs are all considered in evaluating a case’s worth.

Some cases have seen substantial rewards; for example, a recent victim received over $3 million in general damages and nearly $8 million more in punitive damages.

However, these large sums are not guaranteed as each claim’s outcome depends on its unique circumstances.

Speaking with an experienced transvaginal mesh attorney will help you understand better what to expect from your particular scenario.

Latest Updates on Transvaginal Mesh Lawsuits

Discover recent events surrounding transvaginal mesh lawsuits, including updates on recalls, notable verdicts and settlements, as well as latest FDA warnings.

Latest Updates on Transvaginal Mesh Lawsuits

Stay informed and learn why these updates may significantly impact your case.

Read on for more comprehensive information.

Vaginal Mesh Recalls

Several manufacturers have recalled their transvaginal mesh products due to safety concerns.

Here are some of the significant recalls:

  1. Johnson & Johnson’s Ethicon division voluntarily withdrew four models of their mesh products in 2012.
  2. In the same year, Boston Scientific faced a recall of its Pinnacle Pelvic Floor Repair Kit after allegations of faulty design.
  3. C.R. Bard also had two major recalls in 2007 and 2013, pulling thousands of Avaulta Plus BioSynthetic and Avaulta Solo Synthetic systems from the market.
  4. American Medical Systems has had multiple recalls since 2005 including Elevate Anterior and Apogee Vault Suspension system.
  5. The FDA issued a mandatory recall for Transobturator Surgical Mesh Kits produced by PIP Interpoly Implants.due to high failure rates and severe complications.

Verdicts and Settlements

Transvaginal mesh lawsuits have delivered significant verdicts and settlements awarded to victims.

  • In 2019, almost $8 billion went into the pockets of those affected due to settlements and verdicts in transvaginal mesh lawsuits.
  • A notable case involved a New Jersey jury which granted a victim $7.76 million in punitive damages and a separate settlement of $3.35 million.
  • These legal cases are primarily centered around pelvic mesh used in treating pelvic organ prolapse and stress urinary incontinence.
  • The main accusations against companies include negligence, breaches of warranty, as well as design and manufacturing defects.
  • An overwhelming bulk of these transvaginal mesh lawsuits have been successfully settled, with personal injury compensations totaling around $8 billion.
  • Allegations commonly point out design defects in vaginal mesh products while also accusing device manufacturers of serious misconduct.

FDA Warnings

The US Food and Drug Administration (FDA) has issued multiple warnings related mesh manufacturers and the use of transvaginal mesh implants:

  • The initial concerns about these medical devices surfaced in 2008.
  • In July 2011, a safety alert was raised by the FDA due to serious complications associated with surgical mesh for pelvic organ prolapse repair.
  • A significant step was taken in 2019 when the FDA placed a ban on the use of transvaginal mesh for treating pelvic organ prolapse.
  • Adding to this, in October 2022, the FDA reaffirmed its stance by maintaining the ban on transvaginal placement of surgical mesh.

Contact the Transvaginal Mesh Attorneys at TruLaw

If you’ve experienced vaginal mesh complications, injuries, or adverse effects from a transvaginal mesh implant- you may be eligible to file for the Transvaginal Mesh Lawsuit.

Seek justice with TruLaw’s expert transvaginal mesh attorneys.

Contact the experienced Transvaginal Mesh Lawyers at TruLaw today for a no-obligation consultation.

We’re committed to standing up for victims, ensuring their voices are heard.

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!

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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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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
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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.

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