Hernia Mesh

Get More Qualified Leads Using Facebook

The FDA files show that more than one million hernia repairs are being performed each year in the United States with the overwhelming majority involving the use of hernia mesh. Hernia mesh lawsuits claim the devices caused injuries or complications so severe that people had to have additional surgeries.

Hernia mesh manufacturers have recalled more than 211,000 units of hernia mesh from 2005 to February 2019. Most current hernia mesh lawsuits target Bard’s polypropylene hernia mesh, Ethicon’s Physiomesh, and Atrium’s C-QUR brands. All are the subject of separate multidistrict litigations (MDLs).

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