Hernia Mesh – Consumer Assistance Team

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Each year, thousands of Americans receive hernia meshes from brands such as Atrium®, Bard Davo®l, Coviden®, Ethicon®, and more. However, new and emerging reports have found that many of these hernia meshes may cause patients to suffer from severe adverse side effects.

Hernia mesh manufacturers rushed their products to the marketplace without conducting proper testing. now, thousands of patients have been told they will need to have the hernia mesh removed or replaced.

Serious side effects include infection, migration, organ perforation, erosion, and much more. those that have been impacted are encouraged to come forward and receive a 100% free legal case review with a qualified attorney.

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HERNIA MESHes In The News

June 2025:
The Bard and Covidien hernia mesh MDLs continue progressing. Bard cases rise to 25,015, with new lawsuits still being filed. The Covidien MDL adds six new cases, reaching 2,004.

May 2025:
The Covidien hernia mesh MDL picks its second bellwether trial for July 2026.

January 2025:
An "early pay" option is established for straightforward Bard cases, offering $25,000 for less severe injuries and $2,500 if the mesh was unlinked.

December 2024:
The deadline for selecting the first bellwether trial case in the Covidien MDL is pushed to July 2025. Over 26,000 cases are pending in the hernia mesh MDL.

October 2024:
The Bard hernia mesh multidistrict litigation (MDL 2846) reaches a global resolution, paving the way for injured claimants to receive compensation. This follows seven years of litigation, with over 24,000 cases.

2018-Present:
Consolidating numerous individual lawsuits into multidistrict litigations (MDLs) for various manufacturers.

2016:
Ethicon issued a market withdrawal for its Physiomesh Flexible Composite Mesh.

2015:
A federal judge issues an injunction prohibiting Atrium from manufacturing and distributing the C-QUR product.

2012:
The FDA warns Atrium about its failure to address numerous complaints of infections from the C-QUR mesh.

2011:
C.R. Bard settles 3,000 cases over its Kugel Mesh for $184 million.

2010 onwards:
A significant increase in adverse event reports submitted to the FDA regarding hernia mesh complications.

2005-2007:
C.R. Bard issues several Class 1 and Class 2 recalls for its Kugel Mesh product.

Early 2000s:
Increased use of synthetic surgical mesh for hernia repair becomes widespread.

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HERNIA MESHes LINKED TO serious side effects

HERNIA MESHes LINKED TO serious side effects

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Current allegations

HERNIA MESHes In The News