THOSE WITH HERNIA MESH IMPLANTS THAT FAILED & REQUIRED REPLACEMENT MAY BE ELIGIBLE FOR A SETTLEMENT
Thousands of patients have had to suffer from adverse effects following the implantation of a hernia mesh.
Those have recieved a hernia mesh and suffered adverse side effects or have had multiple surgeries to revise a hernia mesh, may be entitled to compensation.
CASES FILED AGAINST HERNIA MESH COMPANIES
Hernia meshes are used throughout hernia repair surgeries. Nearly 90% of all 800,000 hernia repairs in the United States require the use of a hernia mesh.
However, many patients now argue that several large hernia mesh manufacturers have been selling defective products that caused unecesseary injuries.
Many hernia mesh products were rushed to the marketplace without any scientific study as to the safety of the devices. Now, manufacturers are now silently "withdrawing" their defective meshes that may have otherwise been recalled.
MANUFACTURER – aTRIUM®
MODELS INVOLVED: c-qUR MESH, C-QUR RPM MESH, AND MORE
MANUFACTURER – bARD dAVOL®
MODELS INVOLVED: PERFIX MESH, 3D MAXMESH, AND MUCH MORE
MANUFACTURER - cOVIDIEN®
MODELS INVOLVED: PARIETEX MESH, PARIETIX PROGRIP, AND MUCH MORE
MODELS INVOLVED: PHSYSIOMESH COMPOSITE MESH
100% FREE CASE EVALUATION WITH EXPERIENCED & TRUSTED LAW FIRMS.
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