YOU OR A LOVED ONE MAY BE ELIGIBLE FOR A SETTLEMENT
Thousands of patients have suffered from adverse effects following the implantation of a hernia mesh.
If you or a loved one were received a hernia mesh and suffered adverse side effects or have had multiple surgeries to revise your hernia mesh, you may be entitled to compensation.
OVER 5,000 CASES FILED AGAINST HERNIA MESH COMPANIES TO DATE
Hernia meshes are commonly used in hernia repair surgeries. It is estimated that 90% of all 800,000 hernia repairs in the United States require a hernia mesh.
However, many patients now argue that several large hernia mesh manufacturers have been selling defective products that caused unecesseary injuries.
Hernia mesh products were rushed to the marketplace by their manufacturers without any scientific study as to the safety of the devices. Now, these 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. SEE IF YOU QUALIFY TODAY!
Please seek the advice of a medical professional before making health care decisions. This advertisement is not associated with Atrium®, Bard Davol®, Covidien®, Ethicon®, or any government agency.
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