Hernia Mesh Product List
Last updated: June 11, 2026
This hernia mesh product list provides a broad overview of manufacturers and mesh products commonly researched by people looking into complications, revision surgery, product identification, and related lawsuits.
This page provides general educational information and does not constitute legal advice.
- Why people look up hernia mesh product names
- Manufacturers commonly associated with hernia mesh products
- Examples of hernia mesh products people often research
- Why product identification can matter
- Types of hernia mesh people may see in records
- What records may help identify the product
- How this page helps
Why People Look Up Hernia Mesh Product Names
Many people do not know the exact mesh product used in their surgery until they review operative reports, implant records, or hospital billing records. Once complications arise, identifying the product may become an important step in understanding the medical history and researching whether the device has been discussed in litigation.
Product identification can also help people better understand the type of mesh involved, the manufacturer, and whether the product used materials, coatings, or design features that appear in public reporting or legal claims.
Manufacturers Commonly Associated With Hernia Mesh Products
- Ethicon / Johnson & Johnson
- C. R. Bard / Davol
- Atrium
- Covidien / Medtronic
- W. L. Gore
- TELA Bio
Examples of Hernia Mesh Products People Often Research
- Ethicon Physiomesh
- Ethicon Proceed Surgical Mesh
- Ethicon Prolene Hernia System
- Ethicon Ultrapro Mesh
- Bard / Davol Kugel Patch
- Bard Ventralex Mesh
- Bard Ventralex ST Mesh
- Bard PerFix Plug
- Bard 3DMax Mesh
- Bard Sepramesh
- Bard Composix products
- Atrium C-QUR Mesh
- Atrium ProLite Mesh
- Covidien Parietex Mesh
- Covidien Parietene Mesh
- Covidien Symbotex Mesh
- Covidien ProGrip Mesh
- W. L. Gore DualMesh
- TELA Bio OviTex products
Hernia Mesh Recall History
People often search for a hernia mesh recall list, so it helps to be precise about what has and has not been recalled. Only some hernia mesh products were the subject of formal recalls or market withdrawals, and a product being involved in litigation does not mean it was recalled.
- Bard / Davol Kugel Patch: the subject of a series of recalls between 2005 and 2007, including Class I recalls, after reports that the patch's memory recoil ring could break and lead to bowel perforation or other internal injuries. The Kugel recalls produced an earlier wave of litigation that was resolved years before the current Bard MDL.
- Ethicon Physiomesh Flexible Composite Mesh: withdrawn from the worldwide market in May 2016 after registry data suggested higher rates of recurrence and reoperation after laparoscopic ventral hernia repair compared with similar products. Ethicon characterized it as a voluntary market withdrawal rather than a formal recall.
- Atrium C-QUR Mesh: certain lots were recalled over packaging and sterility-related issues, and Atrium's manufacturing facility operated under FDA consent decree scrutiny in the mid-2010s. The C-QUR litigation has since been largely resolved.
- Covidien ProGrip, Parietex, and Symbotex: these products have not been recalled. They are, however, at the center of the active Covidien litigation, which is why searches for a ProGrip or Parietex recall often come up empty while lawsuit references keep appearing.
For the current status of the litigation surrounding these products, see the main hernia mesh lawsuit page and recent developments in hernia mesh litigation.
Why Product Identification Can Matter
Different hernia mesh products may use different materials, coatings, pore structures, shapes, fixation systems, or absorbable components. Because of that, the exact product used in a surgery can matter when reviewing complications, recurrence, infection, pain, revision procedures, and broader legal questions.
This does not mean every complication points to the same issue or the same type of claim. It does mean the exact product name can be an important part of the overall picture.
Types of Hernia Mesh People May See in Records
- Polypropylene mesh
- Composite mesh
- Coated mesh
- Absorbable or partially absorbable mesh
- Biologic mesh
- Hybrid mesh
- Patch systems
- Plug systems
What Records May Help Identify the Product
People often begin with the operative report from the original hernia repair, hospital billing records, implant logs, or later revision surgery records. In some cases, the product name appears clearly in the chart. In others, identifying the device may require piecing together multiple records.
- Operative reports
- Hospital billing records
- Implant logs or implant stickers
- Surgeon records
- Revision or removal surgery records
How This Page Helps
This page is meant to serve as a general product-reference guide, not a complete database of every model, lot number, or product variation ever sold. It gives readers a starting point for identifying commonly discussed hernia mesh products and understanding which manufacturers are often researched.
Learn More About Hernia Mesh Claims
For a broader overview, visit our Hernia Mesh Lawsuit page and review Recent Developments in Hernia Mesh Litigation.
Find Out If You May Have a Case
If you experienced complications after hernia mesh surgery, including revision surgery, chronic pain, or mesh failure, you can request a free, no-obligation case review on Lawsuit Center. Knowing your mesh product helps, but it is not required to start.
Educational purposes only. Submitting a case review request does not create an attorney-client relationship.
Explore Related Lawsuit Topics
Ready to explore related cases and legal topics? Browse the lawsuit directory or learn how the legal process works.
If you're trying to understand whether this situation may apply to you, you can share a few details below to get started.
Educational purposes only. Submitting this form does not create an attorney-client relationship.
Related Legal Guides
