Company description
Ethicon Physiomesh hernia repair mesh has been pulled from global markets permanently due to high failure rates of the device. Used to repair ventral hernia, or weak spots in the abdominal wall, Ethicon hernia mesh has proven to cause significant injuries and hernia recurrence in many patients.
Approved in 2010 via a short-cut FDA approval process, Ethicon's hernia mesh was only discovered to be dangerous after thousands of patients suffered Physiomesh complications. Now, persons across the nation are filing Physiomesh injury lawsuits against Ethicon to recover compensation for the pain, suffering and losses resulting from hernia mesh injuries and surgery.
