Transvaginal Mesh Lawyer in Chicago

Women may undergo surgery with transvaginal mesh to treat pelvic organ prolapse (POP) or stress urinary incontinence (SUI). However, many are left facing severe transvaginal mesh complications and painful revision surgeries due to defective vaginal mesh products. If you are living with lasting health problems or transvaginal mesh injuries after surgery, you deserve the chance to hold the responsible party accountable.

A Chicago transvaginal mesh lawyer from Salvi, Schostok & Pritchard P.C. can help you pursue compensation for your medical expenses, lost income, pain, and suffering. Our firm has the experience and resources to take on large corporations—and our track record speaks for itself. We have recovered over $2.5 billion on behalf of our deserving clients, including more than 375 case results exceeding $1 million. We are ready to help you. Contact us today for a free consultation to find out more about your legal options.

How Our Vaginal Mesh Lawyers Investigate and Build Your Case

Salvi, Schostok & Pritchard P.C. obtained the largest jury verdict ever awarded to an individual plaintiff in Illinois state history. Our team of top litigators has the skill and resources to hold major corporations accountable for any harm they cause. If you’re considering a vaginal mesh lawsuit, contact us as soon as possible. We provide free consultations so you can explore your options without financial risk.

We know how painful and long the road to recovery is for many clients. Our firm handles transvaginal mesh cases with care throughout the entire process. We employ an evidence-based approach to craft persuasive, tailored arguments specific to each client. A vaginal mesh lawyer from Salvi, Schostok & Pritchard P.C. can:

• Collect and review your medical records, surgical history, and vaginal mesh implant details
• Work with medical experts to explain the dangers of defective mesh
• Examine product design and company testing procedures
• Review any failure to provide adequate warnings to patients of known risks
• Demand maximum compensation for medical bills, lost income, and pain and suffering
• Represent you throughout the legal proceedings, including settlement negotiations or at trial
• Provide guidance and support throughout every stage of the legal process

We work hard to prove that mesh manufacturers prioritize profits over patient safety. A transvaginal mesh attorney from our law firm can also monitor ongoing multidistrict litigation and mass tort proceedings nationwide, which helps us position your case within the broader push for accountability.

Client advocacy is at the forefront of our legal representation, but you don’t have to take our word for it. Our client Pamela W. wrote, “When I was searching for legal assistance for a life-changing experience, I was looking for someone to not only help me, but for a legal team who will also listen. The entire team at Salvi, Schostok & Pritchard P.C. was exactly what I was searching for in a firm.”

Chandan B. says, “I’d like to thank David Rashid and his team at Salvi, Schostok & Pritchard P.C. for their exceptional work on my medical malpractice lawsuit. From start to finish, their expertise, attention to detail, and commitment to my case were evident in every step of the process. They made sure I understood my options, provided unwavering support, and fought relentlessly to secure a favorable outcome. Thanks to their hard work and dedication, I received the justice my family deserved.”

Common Complications and Health Risks Linked to Transvaginal Mesh Implants

Transvaginal mesh lawsuits are more common than you might think. Many patients with pelvic mesh implants experience health complications that can last a lifetime. Common problems include:

• Severe pelvic pain
• Chronic pain
• Mesh erosion through vaginal tissue
• Pain during sexual intercourse
• Bleeding and recurrent infections
• Urinary issues, including incontinence
• Organ perforation and internal scarring
• Multiple corrective surgeries with no guarantee of full recovery

According to the U.S. Food and Drug Administration (FDA), the risks of transvaginal mesh for pelvic organ prolapse outweigh its potential benefits. The agency ordered manufacturers to stop selling and distributing pelvic mesh devices in 2019 due to the serious risks these products posed.

Who May Qualify to File a Vaginal Mesh Lawsuit

You may qualify to file a vaginal mesh case if:

• You had a transvaginal mesh device implanted for pelvic organ prolapse or stress urinary incontinence.
• You experienced serious complications such as erosion, pain, or organ damage.
• You required revision surgery or continue to live with chronic symptoms.

Even if your implant surgery occurred years ago, you may still have a valid claim. Vaginal mesh lawsuits often fall under product liability law, which allows patients to pursue compensation when a manufacturer sells a defective or dangerous medical device. However, Illinois has statutes of limitations and repose that restrict how long you are able to file. If you’re experiencing complications, act quickly and speak with an experienced vaginal mesh lawyer. If you wait too long to file, you may lose your chance to recover compensation.

The History of Transvaginal Mesh Recalls and FDA Warnings

Surgical mesh has been used for hernia repair since the 1950s. By the 1970s, medical research and development teams began modifying surgical mesh for other uses.

Transvaginal mesh products first gained FDA clearance in the 1990s through the agency’s 510(k) process. This allowed manufacturers to market these new devices by showing they were “substantially equivalent” to existing surgical mesh products. This pathway did not require rigorous additional clinical testing, which left patients vulnerable to potential risks.

Over time, the FDA received thousands of reports describing serious complications associated with vaginal mesh products. In 2008, the FDA issued a Public Health Notification about risks linked to mesh for pelvic organ prolapse and stress urinary incontinence. By 2011, the agency updated its safety communication, stating that serious injuries and complications were not rare.

In 2016, the FDA reclassified surgical mesh for transvaginal repair of pelvic organ prolapse as a Class III high-risk device, requiring premarket approval. Finally, in 2019, the FDA ordered all manufacturers to stop selling and distributing mesh for pelvic organ prolapse after determining they could not reasonably assure the product’s safety and effectiveness.

Contact Our Chicago Transvaginal Mesh Lawyers for a Free Consultation

If you suffered complications after a mesh implant, we can help you pursue compensation. A Chicago transvaginal mesh lawyer from Salvi, Schostok & Pritchard P.C. can fight to hold manufacturers accountable for any harm caused by transvaginal mesh and other defective medical devices.

Contact us today for a free consultation to review your claim.