Hernia Mesh Legal Leads Tailored to Your Need!
Grow your practice today with qualified hernia mesh live-transfer leads!
Live Transfer Leads
Intake Form
Guaranteed
Compliant Leads
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Live Transfer Leads
Intake Form
Guaranteed
Compliant Leads
Quality Guarantee
All of our Hernia Mesh Live Transfer Mass Tort Leads come with the following guarantees, or your lead will be replaced at no additional cost.
Client has a confirmed injury.
Client’s injury is between your firm’s criteria dates.
Client hernia mesh was either cut, trimmed and/or removed due to mesh failure.
Not working with any other attorneys.
100% exclusive to your company – never resold!
100% Opt-In TCPA Compliant
100%Satisfaction Guarantee
Inquire NowHernia Mesh Legal Leads
According to the FDA, over one million revision hernia mesh surgeries are performed annually in the United States and about 20 million surgeries are performed worldwide.
At The Legal Leads, we pride ourselves in generating premium hernia mesh live-transfer legal leads and signed retainers for claimants who have endured complications from hernia mesh implant surgeries and revisions customized to your firm’s criteria dates. Complications associated with hernia mesh implants can include abdominal pain, infections, bowel obstruction, and perforation of organs and tissue.
Claimants are contacted by one of our trained intake agents and taken through an extensive pre-qualification application that is customized to fit your firm’s criteria, and then receive a phone call with our in-house quality control department to verify all information before it is live transferred to your firm via email, API configuration or post URL along with their application. This process ensures that we send the highest quality hernia mesh legal leads to our partners and leaves minimal room for any lead that is not qualified.
Why choose The Legal Leads? Our leads are meticulously verified to ensure they meet the specific criteria required by most law firms, providing a higher success rate for your cases. We sell live transfer leads and offer a Cost Per Acquisition (CPA) model to help lower the cost of buying low quality leads and also offer guaranteed filters or your hernia mesh legal lead will be replaced at no cost to you. Our dedicated team provides continuous support to ensure your firm achieves the best results.
How It Works
100% Exclusive Hernia Mesh Leads
Through the various means of marketing we deploy, including landing pages, radio, tv, & social media, we receive the initial inquiry from the potential client.
Depending on the tort, our trained intake agents run the potential client through an extensive intake form.
The potential clients is then transferred to our in-house quality control department to verify that all information on the intake form is correct.
Your team will then receive the live-transfer lead via email, API Configuration, or post URL
All Mass Tort Leads Are Delivered in Real-Time
Leads will be instantly delivered to your email of choosing.
Fully integrate the process of acquiring leads with your API.
Deliver new leads via HTTP POST to a URL of your choosing.
23 Question Intake Form
All of our Hernia Mesh Live Transfer Leads come with a rigorous, fully-customizable 23 question intake form mini application. Here is a sample of an intake form for these Hernia Mesh legal leads.
Download Now!Custom intake form - Use you firms intake!
What is the Hernia Mesh Implant Procedure?
Hernias occur when an organ or tissue pushes through a weak spot in the surrounding muscle or connective tissue. A hernia mesh implant is a medical device used to provide additional support to weakened or damaged tissue during hernia repair surgery. The surgeon places the mesh over the afflicted area and secures it with sutures, staples or glue. The procedure for a hernia mesh implant can be done through open surgery or minimally invasive laparoscopic surgery.
Manufacturing Defects in Hernia Mesh
While hernia mesh implants have been beneficial for many patients, there have been numerous reports of complications due to manufacturing defects. These defects can lead to severe health issues that would require medical intervention.
Common Manufacturing Defects
1. Mesh Erosion: This occurs when mesh wears away or disintegrates causing damage to the surrounding tissue and organs.
2. Mesh Shrinkage: Some meshes shrink over time, leading to the tension and pain in the implanted area.
3. Adhesion Formation: Defective meshes can cause scar tissue to form abnormally, leading to chronic pain and complications.
4. Infection: Poorly manufactures meshes can harbor bacteria, leading to severe infections that are difficult to treat.
5. Migration: Some meshes may move from their original position, causing blockages, perforations or other serious issues.
Patients with defective hernia mesh implants have reported a range of complications, including: chronic pain, hernia recurrence, bowel obstruction, and organ perforation.
Which Manufacturers Failed to Warn the Public?
Several manufacturers of hernia mesh products have faced lawsuits in failure to warn the public about the potential risks and complications associated with their devices. These companies include:
1.
Ethicon (a subsidiary of Johnson and Johnson)
Ethicon has faced numerous lawsuits related to its Physiomesh and Prolene hernia mesh products.
2.
C.R. Bard
C.R. Bard is another major manufacturer of hernia mesh products, including the Composix, Kugel and Ventralex meshes.
3.
Atrium Medical Corp
Atrium has been sued over its C-QUR mesh, which is coated with a fish oil derivative intended to reduce inflammation. However, many patients have experienced severe inflammatory reactions and other complications.
3.
Covidien (a subsidiary of Medtronic)
Covidien manufactures several types of hernia mesh, including Parietex.
About the Hernia Mesh Lawsuit
The hernia mesh lawsuit involves numerous plaintiffs who have experienced severe complications following a hernia mesh implant procedure. Complications including infections, organ perforation and mesh migration, ultimately requiring additional surgeries to correct the issues. The lawsuits allege that manufacturers, like Ethicon and C.R. Bard, have failed to properly test their products and did not adequately warn the public and medical community about the potential risks.
As of 2024, thousands of individual hernia mesh lawsuits have consolidated into multi-district litigation (MDL) to streamline pretrial proceedings and potentially reach settlements more efficiently. The FDA reports that over one million hernia mesh revisions are performed annually in the U.S. alone, highlighting the widespread impact of these products.
Hernia Mesh Lawsuit Update 2024
1.
Ongoing Settlement Discussions: As of June 2024, momentum is building toward reaching a global settlement for the Bard hernia mesh MDL. Despite mediation sessions, a comprehensive settlement has not yet been achieved. If a settlement is not reached by the end of 2024, cases may be remanded to district courts for individual trials.
2.
Bellwether Trials: The third bellwether trial, Stinson v. C.R. Bard, resulted in a $500,000 verdict for the plaintiff in November 2023. The fourth bellwether trial involving plaintiff Jacob Bryan was scheduled for April 2024 but was postponed to allow for further settlement discussions.
3.
Increase in Pending Cases:The number of pending cases in the Bard hernia mesh MDL has continued to grow, with over 22,896 cases as of June 2024. May 2024 displayed an increase of 640 new cases, indicating the ongoing influx of new claims related to hernia mesh manufacturing defects and complications.
4.
Confidential Settlements: Johnson and Johnson and its subsidiary Ethicon settled 224 cases in a Georgia MDL, emphasizing the ongoing efforts to resolve claims quietly.
Customization Options: Building Campaigns Your Way
Explore the limitless potential of your legal marketing strategy with our diverse customization options. From tailoring Google and Facebook ads campaigns to match your brand and objectives, to crafting precision messages that resonate with your target audience.
Customize campaigns to align with your goals.
Personalize campaigns to fit your budget.
Target keywords that matter most to you.
Focus on specific regions that are key to your practice.
Customize reporting for insights that matter.
Three-Step Lead Verification Process
1.
Initial Inquiry and Certification
Upon inquiry, leads undergo a preliminary check using lead certification technologies such as Jornaya and TrustedForm.
2.
Email and Information Confirmation
Following their initial interaction, leads are prompted via email and on our thank-you pages to verify their email addresses and the accuracy of their submitted information.
3.
Final Verification
Before a lead is passed to our clients, it undergoes a final verification where the lead confirms their eligibility criteria, such as their diagnosis, via a comprehensive verification form.
Ensuring Quality and Compliance
Each step in our process is designed to build a reliable pipeline of qualified mass tort leads that meet the specific criteria of law firms. By maintaining stringent quality controls and adhering to compliance standards, we ensure that every lead provided maximizes potential case outcomes and ROI for our clients.
Glossary
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