Hernia Mesh Lawsuit
(Davol/C.R. Bard)
The largest medical device MDL in the federal court system. Plaintiffs allege that polypropylene hernia mesh products caused serious complications including chronic pain, mesh migration, organ perforation, and infections requiring additional surgeries.
Key Takeaways
- Over 23,300 cases pending — the largest medical device MDL and the #2 MDL overall, behind J&J talc
- A global settlement framework was announced by BD (Bard's parent) in 2024 — reported to cover ~38,000 claims — so the litigation is now largely in settlement administration. BD said it was defending about 7,090 hernia claims as of June 30, 2026, with no trials scheduled
- Over 1 million hernia mesh repairs performed annually in the U.S.
- Reported complication rate of 10-15% for polypropylene mesh
- Allegations include chronic pain, mesh migration, and organ perforation
- Defendants include Davol, C.R. Bard, and BD (Becton Dickinson)
Key Facts (October 2026)
| Pending Actions | 23,324+ cases in federal MDL |
| Total Actions Filed | 25,217+ cases |
| Defendants | Davol Inc., C.R. Bard Inc., BD (Becton Dickinson) |
| Presiding Judge | Hon. Edmund A. Sargus Jr. (S.D. Ohio) |
| MDL Created | August 2018 |
| Settlement Status | Global settlement framework (BD, 2024); reported ~38,000 claims; Qualified Settlement Fund created by CMO 56; Intensive Settlement Process sessions begin on or about Jan. 4, 2027 |
| Claims BD Is Defending | About 7,090 as of June 30, 2026 (BD 10-Q); no trials currently scheduled |
| Parent Company | BD (Becton Dickinson) acquired Bard in 2017 |
| Can You Still File? | Yes, new cases still being accepted |
Case Resolution Progress
The largest medical device MDL, now largely in settlement administration. BD (Bard's parent) announced a global settlement framework in 2024, reported to cover roughly 38,000 claims; the very high pending count reflects claims parked on the docket during claim review and payment through a Qualified Settlement Fund — not active pretrial litigation. About 777 cases have been resolved since January 2025.
Source: JPML MDL Statistics Reports, January 2025-October 2026
1 What Is This Lawsuit About?
Hernia mesh is a surgical implant used to reinforce weakened tissue during hernia repair surgery. Approximately one million hernia repairs are performed in the United States each year, with the vast majority using mesh. This MDL consolidates cases against Davol Inc. and C.R. Bard Inc. (now owned by BD/Becton Dickinson).
Plaintiffs allege that polypropylene mesh products are defectively designed and can cause serious complications. The material can shrink, degrade, and trigger chronic inflammation. Many patients require painful revision surgeries to remove mesh that has adhered to organs or caused infections.
2 Complications Linked to Hernia Mesh
Plaintiffs in this MDL allege they suffered serious complications from Bard/Davol hernia mesh products:
Mesh Failure
- Mesh shrinkage and contraction
- Migration from original implant site
- Hernia recurrence requiring additional surgery
Organ & Tissue Damage
- Bowel or bladder perforation
- Adhesion to organs and surrounding tissue
- Fistula formation
Chronic Pain
- Persistent groin or abdominal pain
- Nerve damage and entrapment
- Limited mobility and reduced quality of life
Infection
- Chronic infection at mesh site
- Abscess formation
- Sepsis in severe cases
3 Products Involved
This MDL covers various Bard/Davol hernia mesh products, including but not limited to:
- Bard 3DMax Mesh
- Bard Ventralex
- Bard Ventralight ST
- Bard PerFix Plug
- Bard Composix
- Bard Sepramesh
- Bard Kugel Mesh
- Other polypropylene mesh products
Note: This MDL specifically covers Bard/Davol products. Other hernia mesh manufacturers (Ethicon, Atrium, Covidien) have separate MDLs or litigation.
4 Do You Qualify for Compensation?
You may be eligible to file a claim if you meet these criteria:
Eligibility Requirements
- Had hernia repair surgery using a Bard or Davol mesh product
- Experienced complications such as chronic pain, infection, mesh migration, or organ damage
- Required revision surgery to remove, repair, or replace the mesh
- Have medical records documenting your mesh implant and subsequent complications
5 Frequently Asked Questions
How do I know if I have Bard mesh?
What settlements have been reached?
Is it too late to file a claim?
Do I need revision surgery to file?
How long do hernia mesh cases take?
Sources & References
6 official sources cited• Judicial Panel on Multidistrict Litigation (JPML) — Official MDL statistics
• U.S. District Court, Southern District of Ohio — MDL-2846 docket, including Case Management Orders 55 (Nov. 21, 2024) and 56 (Dec. 16, 2024)
• Becton, Dickinson and Company (BD) — Form 10-Q for the quarter ended June 30, 2026 (filed August 6, 2026)
• BD press release on hernia settlement agreements (October 2, 2024)
• FDA Medical Device Database — Hernia mesh adverse event reports
• American Hernia Society guidelines and research
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Every case is unique, and results depend on the specific facts and circumstances involved. Past settlement amounts and case outcomes do not guarantee similar results in your case. If you believe you have a legal claim, you should consult with a licensed attorney in your jurisdiction who can evaluate your specific situation.