TriMark Legal Funding is America’s leading lawsuit loan company providing legal funding to struggling plaintiffs. When the situation gets tough and messy, pre-settlement funding is a fast and risk-free way to break free from financial distress.
Transvaginal mesh complications have taken a tremendous toll on women’s physical, mental, and financial stability. A transvaginal lawsuit loan may help you fix the money issues first, getting the costs of treatment and recovery out of the way.
Aside from the medical risks associated with transvaginal mesh, you won’t be able to escape the bumps and turns of the lawsuit process. It can be long and complicated and lengthy, especially if you’re going against a big pharma facing hundreds or thousands of cases.
This may add to your emotional suffering as you heal from defective transvaginal mesh injuries.
The longer all of this takes, the more money you’ll need for out-of-pocket expenses. To ride out your claim and tide you over, you may want to consider applying for pre settlement funding.
TriMark’s got your back. You can obtain funding fast, risk-free, and for affordably through our non-recourse lawsuit cash advance.
Transvaginal Mesh Pre Settlement Loans
In 2019, there were more than 100,000 people filed claims against the major manufacturers of transvaginal mesh in federal and state courts. In the same year, faulty transvaginal mesh claims were reported as one of the largest mass tort cases in America in terms of damage claims filed, listed corporate defendants, and compensation.
Plaintiffs with a transvaginal lawsuit who are in a financial bind are eligible to receive financing through pre-settlement funding.
Our pre-settlement loans come in the form of settlement cash advances of up to 20% of your anticipated net value. Our loans are non-recourse, which means no monthly fees. If your case doesn’t settle, you are not obliged to return the remaining money in your hands.
Get Pre Settlement Funding Now
Cut through the confusion and get pre-settlement funding now!
In just 3 simple steps, you can advance a portion of your settlement and stop putting off payments for your medical bills and living expenses.
Make sure to read our eligibility checklist before completing the online application. You can also call us toll-free at (877) 932-2628 to have one our legal funding representatives receive your application.
We’ll review your case based on the documents you submitted. After you’re approved, you can receive the funds through your preferred channel, in just 24 hours or less.
Transvaginal Mesh Pre Settlement Funding and Post Settlement Funding
If your case involves a defective product, it falls under product liability lawsuits. This category is eligible for both pre settlement and post settlement lawsuit funding.
The main difference between the two is in which stage of your lawsuit you’re applying for a transvaginal mesh lawsuit loan.
But both loan types are matched with Trimark’s low, non-compounding rates, which count among the most competitive in the industry.
A post settlement loan may also yield more funds because you’re at the end stages of the legal process. For instance, our post settlement transvaginal mesh lawsuit loans can go as high as 50% of the net value of your settled multi-district litigation (MDL) case.
How to Qualify for Vaginal Mesh Lawsuit Loans
These are the criteria for eligibility for transvaginal mesh lawsuit loans for pending cases:
- You are represented by a contingent-fee attorney.
- You must have sustained a significant injury from the use of surgical mesh.
- Your anticipated value should net at least $150,000 (gross award less attorney fees, case costs, medical liens, etc.).
- Your settlement check must be deposited to, and be distributed out of, your attorney’s trust account.
Settled cases are assessed based on their settlement offer or award. You must provide documentation showing that you will net a minimum of $60,000 after all deductions.
What Is Transvaginal Mesh?
The Food and Drug Administration approved the first transvaginal mesh, a medical device used to treat pelvic floor dysfunctions, in 1996. It was marketed as an easy and effective solution to individuals with weakened support to their pelvic organs, such as the bladder, uterus, rectum, and prostate. It is made from synthetic materials or animal tissue.
Primarily, this surgical mesh can treat the following conditions:
Pelvic Organ Prolapse (POP)
Muscles and ligaments support pelvic organs. When this support structure weakens, typically due to aging or multiple vaginal childbirth, the pelvic organs can drop or press into/bulge out of the vagina. The result is known as pelvic organ prolapse (POP).
Symptoms may include seeing or feeling the bulge, pain or discomfort in the pelvis, and leaking urine. The signs and causes differ from person to person.
There are two ways to treat POP: inserting a mesh through abdominal surgery and transvaginal surgery without mesh. Meanwhile, the use of surgical mesh transvaginally was banned by the FDA in 2019 and all transvaginal mesh products were recalled.
Stress Urinary Incontinence (SUI)
Two things: urinary incontinence is the unintentional loss of urine, and stress incontinence results from bladder pressure caused by a sudden physical activity, such as laughing, coughing, or sneezing.
Stress urinary incontinence has nothing to do with psychological stress and is much more common in women.
When someone experiences leaking urine this way, they may be too embarrassed to participate in activities that can trigger SUI. Fortunately, treatment is available to help them manage the symptoms.
Surgery is one of the most common methods of repair in this regard. A mesh, animal tissue, or human tissue can be sutured to create sling-like support for the urethra. Behavioral therapies, medication, and devices can also work, depending on the patient’s case.
Top Manufacturers of Vaginal Mesh
- Johnson & Johnson: This large multinational company markets its pelvic floor repair system products through subsidiary Ethicon.
- Boston Scientific: Leading with ProteGen, the first mesh to be cleared by the FDA for SUI, Boston Scientific is a pioneer in the vaginal mesh market.
- C.R. Bard: Becton Dickinson acquired this developer, manufacturer, and marketer of vaginal mesh implants and other medical technology products in 2017.
- American Medical Solutions: In 2011, his maker of surgical mesh became a wholly-owned subsidiary of Endo Pharmaceuticals, now known as Endo Health Solutions.
- Coloplast: This Danish multinational company creates medical devices for continence, ostomy, urology, and wound care.
FDA Ban on Surgical Mesh
The FDA banned transvaginal mesh intended for the treatment of pelvic organ prolapse in April 2019. The agency found the devices manufactured by Boston Scientific and Coloplast lacked evidence that they’re better than surgery without mesh in repairing POP. This requirement was crucial in the premarket approval applications for Class III medical products.
Transvaginal mesh for POP repair was reclassified into a high-risk device in 2016, following reports of its complications from thousands of patients and physicians.
According to various studies done in BioMed Research International, complications have occurred at a rate of 15% to 25%.
The most common complications submitted to the FDA between 2005 and 2010 are as follows:
|COMPLICATIONS||NUMBER OF REPORTS|
|Dyspareunia (painful sex)||108|
Complications related to treating SUI include mesh erosion and urinary problems. Yet, SUI mesh sling surgeries have been found successful among 70% to 80% women one year.
These are the issues frequently reported to the FDA:
- Mesh erosion
- Urinary problems
- Recurrent incontinence
- Pain during sexual intercourse (dyspareunia)
- Organ perforation
- Neuro-muscular problems
- Vaginal scarring
Claims Against Surgical Mesh Manufacturers
Plaintiffs of the surgical mesh suits have alleged that manufacturers neglected their duty to ensure their devices are safe and effective. Instead, the companies provided false and misleading information, as well as insufficient evidence. Regardless, the products were cleared for use.
According to DrugWatch, the claims were based on the following allegations:
- Intentional misleading of the FDA, the medical community, patients, and the public regarding the products’ safety and effectiveness;
- Failure to test the devices properly;
- Failure to research the risk of the products;
- Failure to create safe and effective mesh removal methods; and
- Failure to sufficiently warn people of potential complications and injuries.
Settlement & Verdict
There are two ways to apply for transvaginal mesh lawsuit loans. And it’s quick and easy!
- You can either fill out an application form online or call to speak with one of our friendly legal funding experts.
- We won’t ask for your credit score, employment history, or income status. We will assess your transvaginal mesh lawsuit loan application based on your case’s merits, so make sure your documents are complete before applying.
- After that, we’ll let you know if your case is approved. Within one to 24 hours, you will receive your funds through your chosen disbursement channel.