Transvaginal Mesh Alternatives

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Jessica Paluch-Hoerman

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

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

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

Key takeaways:

  • Transvaginal mesh is a surgical tool used for treating stress urinary incontinence (SUI) and pelvic organ prolapse (POP), but it can have serious health risks.
  • Alternatives to transvaginal mesh include pelvic floor therapy, medical treatments, and Kegel exercises which strengthen the muscles that support our organs.
  • Natural tissue grafts and traditional surgeries are other options instead of using a transvaginal mesh implant.
  • If you've had problems with a transvaginal mesh implant, legal help like TruLaw can assist you.

Overview of Transvaginal Mesh Alternatives

On this page, we’ll provide an overview of Transvaginal Mesh alternatives, risks and complications associated with Transvaginal Mesh implants, surgical and non-surgical Transvaginal Mesh alternatives, and much more.

There are several transvaginal mesh alternatives for the treatment of pelvic organ prolapse and stress urinary incontinence.

The alternatives to a transvaginal mesh implant include:

  1. Native tissue repair: This surgical treatment involves using the patient’s own tissue to repair the prolapse. It can be an effective alternative to mesh implants.
  2. Biological graft repair: This approach uses a graft from a source such as human or animal tissue to support the vaginal prolapse. It provides a natural alternative to synthetic mesh.
  3. Pubovaginal sling: This procedure utilizes the patient’s own tissue to create a sling that supports the bladder and urethra. It can be an effective alternative for stress urinary incontinence.

Transvaginal Mesh Alternatives; Transvaginal Mesh Lawsuits; Transvaginal Mesh Alternatives; Other Alternatives to Vaginal Mesh Implants; Transvaginal Mesh Lawsuits (1)

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 Alternatives

Native Tissue Repair

Native tissue repair is a surgical treatment that uses the patient’s own tissue to repair pelvic organ prolapse.

Transvaginal Mesh Alternatives

This approach avoids the use of synthetic mesh and can provide effective support for the prolapsed organs.

Some key points about native tissue repair include:

  • Native tissue repair is a safe and effective alternative to transvaginal mesh implants for pelvic organ prolapse.
  • The procedure involves using the patient’s own tissue to create support for the prolapsed organs.
  • Native tissue repair has been shown to have good long-term outcomes and patient satisfaction.

Biological Graft Repair

Biological graft repair is another alternative to transvaginal mesh implants.

This approach involves using a graft from a source such as human or animal tissue to support the vaginal prolapse.

Some key points about biological graft repair include:

  • Biological graft repair provides a natural alternative to synthetic mesh for pelvic organ prolapse.
  • The graft is used to provide support and reinforcement to the weakened vaginal tissues.
  • Biological graft repair has been shown to have good success rates and low complication rates.

Pubovaginal Sling

Pubovaginal sling is a surgical procedure that uses the patient’s own tissue to create a sling that supports the bladder and urethra.

It can be an effective alternative for stress urinary incontinence.

Some key points about pubovaginal sling include:

  • Pubovaginal sling is a safe and effective alternative to transvaginal mesh implants for stress urinary incontinence.
  • The procedure involves using the patient’s own tissue to create a sling that supports the bladder and urethra.
  • Pubovaginal sling has been shown to have high success rates in treating stress urinary incontinence.

In conclusion, there are several alternatives to transvaginal mesh implants for the treatment of pelvic organ prolapse and stress urinary incontinence.

These alternatives include native tissue repair, biological graft repair, and pubovaginal sling.

Transvaginal Mesh Alternatives

Transvaginal mesh is a medical device designed to support weakened pelvic tissues.

Predominantly made from Type I monofilament, large-pore polypropylene mesh, this urogynecological tool serves the purpose of treating specific conditions such as stress urinary incontinence and pelvic organ prolapse.

It is surgically implanted into the pelvic region providing reinforcement and stability.

The utilization of transvaginal mesh became a widely adopted practice owing to its lower rates of prolapse awareness, repeat surgery, and protrusion upon examination.

However, it’s crucial for women to understand that transvaginal mesh isn’t synonymous with laparoscopic procedures or mesh slings.

Each carries separate implications and uses tailored to address distinct medical conditions.

Unfortunately, it can lead to severe complications impacting a woman’s physical and emotional health.

Non-surgical practices such as pelvic floor therapy, medications, and strength-building exercises like Kegels serve as viable alternatives.

There are also different surgical approaches that do not involve the transvaginal mesh, but instead use traditional surgeries or natural tissue grafts.

Transvaginal Mesh Lawsuits; Transvaginal Mesh Alternatives

Manufacturers have come under heavy scrutiny for producing this harmful device and numerous lawsuits have been filed against them, leading to settlements in favor of the victims.

New technological advances have given rise to other alternatives such as Transobturator tape (TOT), tension-free transvaginal tape (TVT), and adjustable slings which are gaining popularity among medical professionals for treating SUI & POP.

When is Transvaginal Mesh Used?

Transvaginal mesh is primarily used in treating conditions such as Stress Urinary Incontinence (SUI) and Pelvic Organ Prolapse (POP), this involves a surgical procedure that provides support to weakened pelvic organs.

When is Transvaginal Mesh Used

Dive deeper into the usage, effectiveness, and potential risks of transvaginal mesh in the following sections.

Explanation of the conditions it is used for (SUI and POP)

Surgeons commonly use transvaginal mesh to treat two specific conditions: Stress urinary incontinence (SUI) and pelvic organ prolapse (POP). SUI is a medical condition where pressure on the bladder leads to involuntary leakage of urine.

Activities such as sneezing, laughing, lifting heavy objects or exercise can trigger this. Women often experience it due to weakened pelvic muscles following childbirth, with age being another significant risk factor.

On the other hand, POP happens when one or more of the pelvic organs slip down from their regular position and protrude into the vagina due to loss of support from surrounding muscles and tissues.

This causes discomfort and complications like constipation or difficulties during intercourse.

Procedures that involve implanting a surgical mesh through the vaginal wall provide reinforcement for weakened structures are typically performed when non-surgical treatments fail to address these issues effectively.

Transvaginal Mesh Surgical Procedure

Transvaginal mesh surgery is a treatment option for women suffering from conditions like stress urinary incontinence and pelvic organ prolapse.

The steps of the transvaginal mesh surgical procedure include:

  • The procedure commences with an incision being made into the vaginal wall.
  • A piece of surgical mesh is then inserted through this incision.
  • The purpose of this mesh is to provide much – needed support to the prolapsed organs.
  • Transvaginal permanent mesh, one type in use, has shown lower rates of prolapse awareness and repeat surgeries that are required.
  • While effective, such surgery is usually considered only after non – surgical treatments fail to offer relief.

Risks and Complications Associated with Transvaginal Mesh Implants

Transvaginal mesh implants can lead to various physical and emotional complications such as infection, bleeding, pain during intercourse and even organ perforation; these issues emphasize the importance of being informed before choosing a course of action.

Risks and Complications Associated with Transvaginal Mesh Implants

Dive deeper into this matter to learn more about potential risks and find safer alternatives for you.

Transvaginal Mesh Implants: Common Complications

While transvaginal mesh can successfully treat pelvic organ prolapse and stress urinary incontinence, it is often associated with a host of complications and side effects.

The following are commonly reported:

  1. Mesh exposure: This tops the list as the most frequent complication. The synthetic mesh tends to erode, leading to discomfort and inflammation.
  2. Excruciating Pain: Women may experience chronic pelvic pain or discomfort during sexual intercourse due to the implanted mesh.
  3. Urgency urinary incontinence: Some women face difficulty controlling their bladder post-surgery, resulting in sudden urges to urinate.
  4. Irregular vaginal discharge or bleeding: As an aftermath of surgery, women might notice abnormal discharge or bleeding.
  5. Pelvic swelling: Swelling around the pelvic region is another common complaint after transvaginal mesh implantation.
  6. Infection: Surgical procedures always carry a risk of infection, and implantation of surgical mesh is no different.
  7. Nerve damage: In some cases, nerves may be harmed during the procedure causing neuro-muscular problems.
  8. Organ perforation and tearing: Rare but serious complications include damages to nearby organs such as the bladder, bowel or uterus due to mesh erosion.

The impact on physical and emotional well-being

The physical toll of transvaginal mesh complications can be significant, leading to persistent pain and discomfort.

This chronic pain may arise from poor tissue integration or the formation of additional scar tissue around the surgical site.

It’s common for women who experience these complications not only to face physical challenges, but also suffer emotionally.

Additionally, emotional distress often accompanies these health concerns as they interfere with a woman’s daily life quality.

Constantly dealing with unexpected health problems may lead to feelings of frustration and hopelessness over time which can then evolve into anxiety or depression.

Thus, understanding the potential impact on both physical and emotional well-being is crucial when considering transvaginal mesh implants.

Non-Surgical Alternatives to Transvaginal Mesh

Exploring non-surgical alternatives to transvaginal mesh, we delve into effective methods such as pelvic floor therapy, lifestyle modifications, and prescribed medications that have been successful in treating conditions like Stress Urinary Incontinence (SUI) and Pelvic Organ Prolapse (POP).

Non-Surgical Alternatives to Transvaginal Mesh

Pelvic floor therapy

Pelvic floor therapy stands out as an effective non-surgical alternative to transvaginal mesh.

As part of this therapeutic approach, physical therapy is employed to strengthen pelvic floor muscles and alleviate symptoms of stress urinary incontinence and pelvic organ prolapse.

Unlike surgical implantation of transvaginal mesh, which could potentially lead to complications such as mesh erosion and scar tissue formation, the practice of pelvic floor therapy prioritizes patient comfort and safety.

Moreover, this treatment option offers significant benefits, including lower rates of condition recurrence compared to traditional native tissue repair procedures.

Medications

Several prescription medications prove beneficial in the management of stress urinary incontinence and pelvic organ prolapse.

For instance, anticholinergic drugs or alpha-adrenergic agonists are viable options for women experiencing mild symptoms.

These medicines work by relaxing bladder muscles to control involuntary urine leakage.

Some hormones, mainly topical estrogen therapy, can strengthen your vaginal tissues if you’re postmenopausal.

The hormone treatment improves urinary incontinence by replenishing estrogen levels in the body, thus improving overall health of the pelvic floor muscles.

However, always discuss side effects and potential risks with your healthcare provider before starting any new medication regimen.

Kegel exercises

Kegel exercises have emerged as a simple yet effective alternative to transvaginal mesh implants for treating pelvic organ prolapse and stress urinary incontinence.

These exercises aim to strengthen the pelvic floor muscles that support bladder, uterus, rectum and small intestine.

Some key points about this alternative to transvaginal mesh includes:

  • Regular practice of Kegel exercises can improve control over urine and bowel movements.
  • Most women find these exercises easy to do and require no special equipment or gym memberships.
  • By contracting and relaxing the pelvic floor muscles regularly, women can alleviate symptoms of prolapse and stress urinary incontinence naturally.
  • Kegel exercises are also beneficial post childbirth as they help tighten weakened vaginal muscles.

Surgical Alternatives to Transvaginal Mesh Implants

This section delves into surgical substitutes for transvaginal mesh implants, with a focus on conventional stress urinary incontinence (SUI) and pelvic organ prolapse surgery.

Surgical Alternatives to Transvaginal Mesh Implants

The use of natural tissue grafts as an alternative is also discussed, highlighting the pros, cons and potential outcomes of these procedures.

Traditional SUI and POP surgeries

In traditional surgeries for SUI (Stress Urinary Incontinence) and POP (Pelvic Organ Prolapse), no mesh is used, which serves as an alternative to transvaginal mesh implants.

The procedures involve repairing or reconstructing the natural tissues that hold the pelvic organs in place.

Surgeons utilize stitches to strengthen the weakened muscles and ligaments, facilitating adequate support for pelvic organs like bladder, rectum, and uterus.

While abdominal POP surgery seems to present lower rates of complications compared to its transvaginal counterpart when using a mesh implant, it’s crucial to note that traditional operations without meshes still remain a viable option.

The effectiveness of these surgical options varies depending on each patient’s unique circumstances including:

  • Age
  • Overall health
  • Severity of prolapse
  • Incontinence symptoms
  • Other various factors

The use of natural tissue grafts

Natural tissue grafts serve as a notable alternative to transvaginal mesh implants. Surgeons often utilize the patient’s own tissues or biological material during prolapse surgery, enhancing the outcomes of these procedures.

This surgical option involves using durable materials that are compatible with the human body and can provide similar support and function without some of the risks associated with synthetic meshes.

The benefits of natural tissue grafts extend beyond their compatibility.

These grafts also contribute significantly to reducing complications associated with pelvic floor surgeries.

By harnessing native tissue repair techniques, medical professionals can manage issues such as scar tissue formation or erosion more effectively than when dealing with synthetic implant materials.

While this approach may require careful consideration and skilled surgery, for many women it offers a viable and safer version of treatment for pelvic organ prolapse.

Other Alternatives to Vaginal Mesh Implants

Exploring other alternatives to vaginal mesh implants such as transobturator tape, tension-free transvaginal tape, and adjustable slings can provide safer solutions to urinary incontinence and pelvic organ prolapse without the risks associated with mesh use.

Transvaginal Mesh Lawsuits; Transvaginal Mesh Alternatives; Other Alternatives to Vaginal Mesh Implants;

Transobturator tape

Surgeons often turn to the use of transobturator tape as an alternative for vaginal mesh implants in cases of stress urinary incontinence or pelvic organ prolapse.

This surgical option offers relief when non-surgical treatments fail to generate satisfactory results.

The procedure involves careful placement of a specially designed tape through the obturator foramen, creating a support system for the urethra and bladder neck.

Just like any other surgery, it also carries potential risks that patients should consider before opting for this treatment.

In certain situations when complications arose from using mesh implants, total removal of transobturator tape has successfully resolved these issues.

However, always consult with your healthcare provider to discuss the best solution tailored to your specific medical condition.

Tension-free transvaginal tape

Tension-free transvaginal tape, often referred to as TVT, has emerged as a reliable surgical alternative to transvaginal mesh for women suffering from stress urinary incontinence.

This revolutionary technique offers significant benefits with high satisfaction rates and confirmed safety over long-term use.

Many studies have shown that TVT can help resolve symptoms of bladder control problems effectively and efficiently among many women.

It is also noteworthy that the chances of experiencing pain post this procedure are quite low, making it an acceptable choice for patients concerned about comfort and quality of life after surgery.

Readjustable sling

A readjustable sling offers an innovative solution for pelvic floor reconstructive surgery.

This state-of-the-art device functions as a versatile alternative to traditional transvaginal mesh implants.

Conceived with flexibility in mind, the design enables doctors to make adjustments according to each patient’s unique needs.

Success rates have shown significant improvement with the use of adjustable slings in second-line surgical management after midurethral procedures.

Moreover, this method has demonstrated fewer complications compared to other options, providing patients not only with effective treatment but also peace of mind knowing they are less likely to experience potential issues associated with other surgical interventions.

Leveraging this modern approach could serve as a turning point in managing conditions such as stress urinary incontinence and pelvic organ prolapse.

Manufacturers and Brands of Transvaginal Mesh Implants

There are several manufacturers and brands that produce transvaginal mesh implants, including Johnson & Johnson, Boston Scientific, and Bard Medical.

Manufacturers and Brands of Transvaginal Mesh Implants

Recent years have seen a surge in lawsuits against these companies due to severe complications caused by their products.

Explanation of the various manufacturers and brands

Several manufacturers produce different types of transvaginal mesh.

Each brand has its own design, purpose, and specifications.

Major manufacturers of Transvaginal Mesh include:

  • Johnson & Johnson: Known for their Gynecare Prolift and TVT slings, Johnson & Johnson faced numerous lawsuits for complications related to their mesh products.
  • American Medical Systems (AMS): AMS is another leading manufacturer who had to discontinue the production of their Elevate Anterior and Apical System due to legal issues.
  • Boston Scientific: They offer a variety of urogynecological surgical mesh implants, including Uphold LITE, Pinnacle LITE, and Advantage FIT systems.
  • Coloplast: Known for their Novasilk Synthetic Mesh system and Aris Transobturator Sling system.
  • Bard Medical: Marsupial, Align, Avaulta Solo are some of the brands developed by Bard Medical.

Mention of recent lawsuits against these companies

Major manufacturers of transvaginal mesh like Johnson & Johnson, Boston Scientific, and C.R. Bard find themselves in legal hot water as an influx of lawsuits surface.

Women treated with their products have been reporting severe complications, leading to life-altering conditions.

In light of these disturbing revelations, thousands of affected patients are resorting to the courts for justice.

Since 2012 alone, at least 20 verdicts have gone in favor of these women, tallying an estimated sum of $300 million in damages awarded.

The misconduct allegations brought against these companies range extensively from issues relating to product safety down to their marketing practices.

Transvaginal Mesh Lawsuits

There is significant legal action being pursued against manufacturers of transvaginal mesh due to the serious complications many women have experienced.

Transvaginal Mesh Lawsuits; Transvaginal Mesh Alternatives; Other Alternatives to Vaginal Mesh Implants; Transvaginal Mesh Lawsuits (1)

At TruLaw, we’re dedicated to helping those affected navigate these complex lawsuits and seek the justice they deserve.

Legal Action Taken Against Manufacturers

Several transvaginal mesh manufacturers are currently facing legal actions for their products.

These lawsuits are primarily based on allegations that the companies failed to warn patients and doctors about potential complications related to mesh implants.

In recent years, thousands of legal claims have been resolved favorably for the plaintiffs, with settlements surpassing $8 billion in total.

The main contention is that these devices were marketed without adequate safety testing or alerting users to possible severe side effects such as pain, infection, bleeding and perforation of organs.

TruLaw Can Help

TruLaw extends a helping hand to those negatively impacted by transvaginal mesh implants.

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.

This legal aid includes individuals who’ve suffered complications such as infections, chronic pain, or recurrence of incontinence after surgery.

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.

Conclusion and Call to Action

Exploring alternatives to transvaginal mesh opens up a range of potential solutions that may better suit individual needs and scenarios.

Various Alternatives to Transvaginal Mesh

Nonsurgical actions can involve pelvic floor therapy, medications and regular Kegel exercises – all aimed at strengthening the pelvic muscles.

For those considering surgery, traditional SUI (stress urinary incontinence) and POP (pelvic organ prolapse) operations present an option, as does the use of natural tissue grafts for repair.

Other medical aids such as tension-free vaginal tape or a readjustable sling offer less invasive alternatives for treatment while reducing associated risks and complications.

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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