How to File a Transvaginal Mesh Lawsuit?

Transvaginal mesh complications have affected thousands of women across the United States, leading to numerous lawsuits against medical device manufacturers.

These surgical mesh implants, originally designed to treat pelvic organ prolapse (POP) and stress urinary incontinence (SUI), have been associated with severe complications that can significantly impact quality of life.

Women’s Stories: Life Changes After Mesh Surgery

The impact of transvaginal mesh complications extends far beyond physical symptoms, affecting every aspect of women’s daily lives.

Many survivors have courageously shared their experiences to help others understand the profound changes they’ve endured.

Common experiences reported by women affected by mesh complications include:

• Chronic Pain and Discomfort: – Women report persistent pelvic pain that interferes with basic activities like sitting, walking, or standing. This constant discomfort often prevents them from maintaining regular employment or enjoying family activities.
• Intimate Relationship Changes: – Many women experience severe pain during intimate relations, leading to relationship strain and emotional distress. Some relationships have ended due to the physical and emotional toll of mesh complications.
• Multiple Corrective Surgeries: – Numerous women have undergone multiple revision surgeries attempting to remove damaged mesh and repair tissue, each procedure carrying its own risks and recovery period.
• Mental Health Impact: – The chronic nature of mesh complications has led to depression, anxiety, and loss of self-esteem for many women, requiring ongoing psychological support and counseling.

These personal accounts highlight the long-lasting impact of mesh complications and underscore the importance of legal advocacy for affected individuals.

Seeking Compensation for Physical & Emotional Damage

The pursuit of compensation through transvaginal mesh lawsuits aims to address both tangible and intangible damages suffered by affected women.

Types of damages commonly sought in transvaginal mesh cases:

• Medical Expenses: – Coverage for past and future medical procedures, including mesh removal surgeries, reconstructive procedures, and ongoing treatment for complications. This often includes costs for pain management, physical therapy, and psychological counseling.
• Lost Income and Earning Capacity: – Compensation for work missed due to medical procedures, recovery time, and ongoing complications. This may include projected future income losses if the condition prevents a return to previous employment.
• Pain and Suffering: – Monetary awards for physical pain, emotional distress, and reduced quality of life resulting from mesh complications. Courts consider both past and ongoing suffering when determining compensation.
• Loss of Consortium: – Recognition of the impact on marital relationships, including the loss of companionship and intimate relations due to mesh complications.

The compensation process involves careful documentation of all damages and working with experienced attorneys who understand the complexities of medical device litigation.

Collecting all relevant medical records is an important step in filing a transvaginal mesh lawsuit.

These records provide a comprehensive view of the medical history and complications that have arisen due to using the mesh.

Proper documentation is essential as it serves as evidence and strengthens the claims made in the lawsuit.

Without these records, validating the issues related to the surgical procedure and ongoing complications becomes challenging.

Surgical Records Show Device Information

Surgical records are vital when preparing to file a transvaginal mesh lawsuit as they include detailed information about the type of device implanted.

Typically, surgical records will also show the implant/device log, which provides precise details necessary for establishing the connection between the device and the complications experienced.

Accurate identification of the device is critical for the success of such lawsuits as it directly links the medical issues to a specific cause. Ensuring these records are complete and available before filing is fundamental.

Obtaining medical records involves identifying certain key documents, such as:

• Implant/Device Log: Contains detailed information about the specific product used during surgery.
• Surgical Report: Includes descriptions of the procedure and any deviations from the standard protocol.
• Product Identification: Direct connections between the device information and complications are established.

Having access to the surgical records that show device information is pivotal in constructing a strong case.

It provides the necessary context and foundation to support claims of defect or negligence against manufacturers.

Without these records, proving that a specific device was used and that it caused harm could become significantly more challenging.

Complications Must Be Well Documented Now

Proper documentation of complications is imperative in pursuing a transvaginal mesh lawsuit. Complications such as chronic pain, mesh erosion, and infections must be detailed in the medical records to support the legal claims.

This documentation process not only illustrates the severity of the issues but also helps demonstrate the direct link between the implantation and the resulting health problems.

The absence of clear documentation can weaken the case, making it difficult to prove the extent of harm caused by the mesh implantation.

Thorough documentation of complications should cover several aspects, including but not limited to:

• Nature and Severity of Complications: Details about symptoms like chronic pain or infections.
• Duration and Frequency: Information on how long and how often complications occur.
• Impact on Quality of Life: Descriptions of how these complications affect daily activities and overall well-being.

Documenting complications thoroughly establishes the basis for compensation claims, highlighting how the device has impacted the individual’s health and lifestyle.

By ensuring that every aspect of the complication is recorded, the plaintiff strengthens their position against the manufacturers.

Effective documentation aids in showcasing the progression and persistency of the health issues, which are often essential in achieving favorable outcomes in these lawsuits.

Transvaginal mesh complications have affected thousands of women across the United States, leading to serious physical and emotional trauma.

The surgical mesh, initially marketed as a solution for pelvic organ prolapse (POP) and stress urinary incontinence (SUI), has been associated with severe complications that have prompted FDA warnings and resulted in billions of dollars in settlements.

Women’s Stories: Life Changes After Mesh Surgery

The impact of transvaginal mesh complications extends far beyond physical symptoms, affecting every aspect of women’s daily lives.

Their experiences highlight the devastating consequences of mesh failure and the importance of legal recourse.

Women who have experienced transvaginal mesh complications commonly report the following life-altering changes:

• Chronic Pain and Discomfort: – Many women report persistent pelvic pain that makes simple activities like sitting or walking extremely difficult. This chronic pain often prevents them from maintaining regular employment or enjoying family activities.
• Intimate Relationship Problems: – The mesh complications frequently cause painful intercourse (dyspareunia), leading to significant strain on intimate relationships and affecting both physical and emotional well-being.
• Limited Mobility: – Mesh erosion and organ perforation can severely restrict movement, forcing women to modify or abandon previously enjoyed activities and limiting their independence.
• Psychological Impact: – The ongoing physical symptoms often lead to depression, anxiety, and decreased self-esteem, particularly when multiple surgeries are required to address complications.

The profound impact of these complications has led many women to seek both medical intervention and legal assistance to address their suffering.

Investigating Transvaginal Mesh Failure Rates

The investigation of vaginal mesh implantshas revealed alarming patterns of complications and led to significant regulatory actions.

In April 2019, the FDA ordered all manufacturers to stop selling and distributing transvaginal mesh products for pelvic organ prolapse, citing failure to demonstrate reasonable assurance of safety and effectiveness.

Clinical Studies and FDA Safety Warnings

The evolution of FDA oversight regarding transvaginal mesh has been shaped by mounting clinical evidence and adverse event reports.

Key findings from clinical studies and FDA investigations reveal:

• Complication Rates: – Research shows that approximately 10-12% of women who received transvaginal mesh for POP repair experienced mesh erosion within 12 months of surgery. Long-term studies indicate even higher rates, with some reports showing complications in up to 30% of cases.
• Revision Surgery Requirements: – Studies indicate that between 15-25% of women with mesh implants require additional surgery to address complications. Some patients have needed multiple revision surgeries, with each procedure carrying additional risks.
• FDA Warning Evolution: – The agency issued its first safety communication in 2008, followed by stronger warnings in 2011. By 2016, the FDA reclassified transvaginal mesh for POP repair as a Class III (high-risk) device, culminating in the 2019 sales ban.
• Long-term Outcome Data: – Clinical research has shown that mesh complications can occur years after initial implantation, with some women experiencing problems up to a decade post-surgery.

These findings have been instrumental in supporting legal claims and driving regulatory changes to protect patient safety.

Types of Mesh Products With Known Defects

These specific pelvic mesh products involved in complications helps patients and attorneys build stronger cases. Multiple manufacturers have faced litigation over defective mesh products.

Major manufacturers and their problematic mesh products include:

• Johnson & Johnson (Ethicon): – Products like Gynecare Prolift, TVT, and Prosima have been linked to high failure rates. The company faced a $302 million judgment in California for concealing risks.
• Boston Scientific: – Products, including Pinnacle and Obtryx mesh systems, have resulted in numerous lawsuits.
• C.R. Bard: – The Avaulta product line and other mesh devices led to significant litigation, with the company paying hundreds of millions in settlements.
• American Medical Systems: – Their portfolio of products, including Perigee and Apogee systems, resulted in substantial settlements before the company’s parent corporation, Endo International, filed for bankruptcy protection.

Identifying these specific products and their documented transvaginal mesh implant complications has strengthened the legal position of affected women seeking compensation through the courts.

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

With extensive experience in product liability cases, Jessica Paluch-Hoerman and our partner law firms work with litigation leaders and medical experts to prove how defective mesh implants caused you harm.

TruLaw focuses on securing compensation for medical expenses, revision surgeries, pain and suffering, lost income, and other damages resulting from your transvaginal mesh injuries.

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

Meet the Lead Transvaginal Mesh Attorney at TruLaw

Meet our lead Transvaginal Mesh attorney:

• Jessica Paluch-Hoerman: As founder and managing attorney of TruLaw, Jessica brings her experience in product liability and personal injury to her client-centered approach by prioritizing open communication and personalized attention with her clients. Through TruLaw and partner law firms, Jessica has helped collect over $3 billion on behalf of injured individuals across all 50 states through verdicts and negotiated settlements.

How much does hiring a Transvaginal Mesh lawyer from TruLaw cost?

At TruLaw, we believe financial concerns should never stand in the way of justice.

That’s why we operate on a contingency fee basis—with this approach, you only pay legal fees after you’ve been awarded compensation for your injuries.

If you or a loved one experienced pain, bleeding, infection, organ perforation, mesh erosion, or other complications from transvaginal mesh implants, you may be eligible to seek compensation.

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

Transvaginal mesh lawsuits are being filed by individuals across the country who were injured by these defective medical devices.

TruLaw is currently accepting clients for the transvaginal mesh litigation.

A few reasons to choose TruLaw for your transvaginal mesh lawsuit include:

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

If you or a loved one suffered mesh erosion, organ perforation, or other complications after being implanted with a transvaginal mesh device, you may be eligible to seek compensation.

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