A permanent implant that failed for thousands of patients.
Polypropylene hernia mesh products have been linked to chronic pain, adhesions, erosion, and the need for revision surgery.
- 20,000
- Claims filed
- $1B+ in settlements
- Recovered to date
- 1
- Studies cited
Quick eligibility check
Step 1 of 3
Were you exposed to or treated with this product?
Confidential. No fee unless compensation is recovered.
Overview
Surgical mesh implanted to reinforce hernia repairs has failed for many patients, causing migration, erosion, adhesion, infection, and chronic pain. Multidistrict litigation consolidates claims against several manufacturers, and the outcome depends heavily on the specific product implanted.
Who may qualify
- Surgical implantation of a hernia mesh product (not all products are included)
- A subsequent complication requiring revision surgery, removal, or ongoing treatment
- Medical records identifying the specific manufacturer and product implanted
- Complication occurring within the filing window under your state's law
Documented injuries & conditions
Medical studies & evidence
Long-term Mesh Complication Rates
JAMA Surgery · 2023
Litigation updates
2026-01-18
Bellwether program progresses
Bellwether outcomes have shaped negotiated resolutions for certain products, while other manufacturers' cases continue toward trial.
Frequently asked questions
No — only products named in the litigation are included. Your operative report is used to identify the exact implant.
Your Hernia Mesh Complications claim may still be viable.
Limitations periods vary by state and by claim type. A three-minute review confirms whether your file is still within the filing window.