Oklahoma Hernia Mesh Lawsuit | 2025 Latest Updates

Oklahoma Hernia Mesh Lawsuit Overview

Oklahoma courtrooms are witnessing intense legal battles against prominent medical device manufacturers including Ethicon, C.R. Bard, Covidien, and Atrium Medical Corp in hernia mesh lawsuits.

Primary allegations include defective design, manufacturing defects, and failure to warn about potential complications from hernia mesh implants.

C.R. Bard MDLs alone reached 18,813 pending claims as of February 2023, with nearly 100 additional cases filed in January 2024.

The FDA has documented severe complications associated with hernia mesh devices, with numerous products facing recalls and safety warnings [1].

Recent verdicts have ranged from $60,000 to $1 million, demonstrating the significant impact of these cases.

Latest Oklahoma Hernia Mesh Lawsuit Updates

• June 2, 2025: There were 1,998 cases still active in the federal Covidien MDL, with more than 6,000 cases pending in Massachusetts State Court [2].
• March 2024 – Mediation plans set for Bard litigation with predicted settlements offering potential resolution for thousands of Oklahoma plaintiffs [3].
• September 2023: Six Covidien hernia mesh lawsuits were chosen as the first bellwether trials to provide insight into the potential direction of the litigation [4].
• December 2023 – Ethicon and Johnson & Johnson reached settlement involving 224 lawsuits in Georgia MDL, setting precedent for future dispute resolutions and demonstrating manufacturer willingness to resolve claims [5].

FDA Reports and Statistics

According to the FDA’s 2023 guidance, hernia mesh is designed to provide support to weakened tissue surrounding hernias, but complications have led to numerous legal disputes.

The FDA has documented significant safety concerns with various mesh products.

Key Litigation Statistics:

• 18,813 pending claims in C.R. Bard MDL as of February 2023
• $4.8 million verdict against Becton Dickinson in August 2022
• $500,000 award in Stinson bellwether trial
• $255,000 verdict against C.R. Bard in recent bellwether trial
• $66 million settlement fund established by Atrium in December 2021

FDA-Reported Complications:

• Multiple product recalls and safety warnings issued
• High failure rates documented for certain mesh products
• Severe complications reported to FDA adverse event database
• Manufacturing and design defects identified in various products

Oklahoma Hernia Mesh Injuries & Side Effects

According to 2020 research by Science Direct, hernia mesh complications represent real and often debilitating conditions that have significantly impacted patients’ lives [6].

These complications are especially linked to recalled hernia mesh products as reported to the FDA.

Serious complications include:

• Adhesion and Bowel Obstruction: Mesh causes tissue scarring and intestinal blockages
• Cancer and Erosion: Malignant growths and mesh degradation through surrounding tissue
• Hernia Recurrence and Infections: Original hernia returns with bacterial contamination
• Migration and Perforation: Mesh moves from placement and punctures organs
• Chronic Pain and Seromas: Persistent discomfort and fluid accumulation

Studies have shown that surgical mesh can reduce the rate of hernia recurrence. However, some hernia mesh also has a high failure rate and can cause severe or even life-threatening complications. – National Library of Medicine

Do You Qualify for an Oklahoma Hernia Mesh Lawsuit?

You may qualify for an Oklahoma hernia mesh lawsuit if:

• You underwent hernia mesh surgery in Oklahoma and experienced complications
• You experienced serious side effects including prolonged pain, adhesion, bowel obstruction, cancer, erosion, hernia recurrence, infections, migration, perforation, or seromas
• The injuries required medical treatment, hospitalization, or revision surgery
• You can provide medical documentation linking your injuries to the hernia mesh implant

Key Qualification Factors:

• Identification of hernia mesh brand and manufacturer (Ethicon, Atrium, Covidien, or Bard Davol)
• Documentation of complications requiring further medical intervention
• Medical record review to establish connection between mesh and complications

Evidence Required for an Oklahoma Hernia Mesh Lawsuit

Essential documentation includes:

• Comprehensive Medical Records: Detailed documentation of every procedure, medication, and follow-up appointment related to hernia mesh complications
• Serial Number Confirmation: Hernia mesh implant serial number to directly link patient injuries to specific product and manufacturer
• Legal Documentation: Meticulously prepared legal petitions and summons for proper case filing
• Surgery Records: Complete surgical charts and post-operative documentation

Damages You Can Recover

Oklahoma hernia mesh victims may receive compensation for:

• Medical Bills: Current and future medical expenses including revision surgeries
• Lost Wages: Income lost due to complications and extended recovery periods
• Pain and Suffering: Physical discomfort and emotional distress
• Mental Anguish and Personal Expenses: Psychological impact and additional costs incurred

Oklahoma Hernia Mesh Recall Information

Multiple hernia mesh products have faced recalls and safety concerns, particularly those from major manufacturers:

• Ethicon: Various mesh products subject to litigation and safety concerns
• C.R. Bard: Multiple products including 3DMax mesh involved in extensive litigation
• Covidien: Mesh products named in numerous lawsuits and MDL proceedings
• Atrium Medical Corp: C-QUR mesh and other products subject to $66 million settlement fund

Identifying the specific mesh product used is crucial for determining lawsuit eligibility and connecting complications to responsible manufacturers.

Statute of Limitations for Oklahoma Hernia Mesh Lawsuits

Two years from the date of injury to file a hernia mesh lawsuit. The statute may begin from the date of discovery if injuries were not immediately apparent.

Oklahoma’s two-year limitation period makes immediate legal consultation essential to preserve your rights and ensure proper case development.

Related Article: Ohio Hernia Mesh Lawsuit

FAQs

1. What are the grounds for filing a hernia mesh lawsuit?

Grounds include defective design, manufacturing defects, improper labeling, and medical malpractice. Each claim requires specific evidence to prove that the mesh caused harm.

2. How does a defective design cause hernia mesh failure?

Defective designs can lead to mesh shrinkage, migration, or degradation over time. These defects can cause severe injuries, necessitating further medical intervention.

3. What should I expect during the hernia mesh lawsuit process?

The process includes filing the claim, participating in discovery, engaging in settlement negotiations, and possibly going to trial if settlement isn’t reached. An experienced lawyer guides you through each step.

4. What is the average settlement amount for Oklahoma hernia mesh cases?

Recent verdicts range from $60,000 to $1 million, with predicted settlements of $65,000 to $70,000. Individual amounts depend on injury severity and case specifics.

5. How do Oklahoma hernia mesh lawyers help identify the mesh product?

Lawyers are adept at uncovering medical records or finding alternative ways to determine the mesh brand, especially crucial when products have been recalled.

6. What role do MDLs play in Oklahoma hernia mesh cases?

MDLs consolidate thousands of individual cases against manufacturers to simplify the legal process and facilitate coordinated pretrial proceedings.

7. Can I file a lawsuit if my medical records are hard to find?

Yes, experienced lawyers can help uncover necessary records or find alternative ways to determine the mesh brand and establish your case.

8. What makes bellwether trials important for Oklahoma cases?

Bellwether trials serve as indicators for future cases, influencing settlement negotiations and litigation strategies for thousands of similar claims.

9. How does the severity of my injury affect compensation?

Injury severity plays a pivotal role in settlement outcomes, with more severe complications and need for revision surgeries increasing potential compensation.

10. What happens if a fourth bellwether trial is cancelled?

Cancellations often hint at judicial preference for settlements over prolonged courtroom battles, potentially accelerating resolution negotiations.

See all related medical device lawsuits our attorneys covered so far.

Get Your Free Oklahoma Hernia Mesh Lawsuit Evaluation With Our Lawyers

Schmidt & Clark, LLP stands with you in challenging times. Should you or someone close to you endure the repercussions of hernia mesh complications, don’t hesitate to contact our Oklahoma hernia mesh lawyers.

Our adept team specializes in these complex cases and will navigate you through every step of the legal journey. We’re dedicated to clarifying your legal entitlements and assessing your eligibility for a hernia mesh claim.

We offer free consultations, and our services are contingent upon securing a win for you. Reach out for a thorough case review regarding your hernia mesh concerns.

References

1. https://www.fda.gov/medical-devices/implants-and-prosthetics/surgical-mesh-used-hernia-repair#What
2. https://www.motleyrice.com/medical-devices/hernia-mesh/covidien
3. https://www.lawsuit-information-center.com/bard-hernia-mesh-lawsuits.html
4. https://www.sokolovelaw.com/product-liability/medical-devices/hernia-mesh/
5. https://www.drugwatch.com/news/2023/12/06/jj-and-ethicon-quietly-settle-over-200-hernia-mesh-lawsuits/
6. https://www.sciencedirect.com/science/article/pii/S2666138120300025