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Recalled Hernia Mesh Patch Patients Retain The Johnson Law Firm


The Johnson Law Firm announced today that it is representing hundreds of patients implanted with the recalled and nonrecalled Bard Composix Kugel Hernia Mesh Patch.

The firm recently expanded its claim evaluation criteria to include non-recalled Kugel hernia mesh patches.

The FDA has urged patients determine if they have a Bard Composix Kugel Mesh Hernia Patch that is part of the FDA hernia mesh recall. The U. S. Food and Drug Administration recently issued a “Class 1” recall of these hernia mesh repair patches because the defect associated with the use or exposure to the Bard Composix Kugel Mesh Large Patch has a reasonable probability to cause serious adverse health consequences, including death, according to the FDA.

Patients can view a complete list of the hernia mesh patches in the recall by going to or by calling toll free 1-866-374-0338 and requesting a copy of the FDA Recall Notice.

The FDA has advised patients who have been implanted with the recalled “Kugel Patch” to seek medical attention immediately if they experience symptoms such as unexplained or persistent abdominal pain, fever, tenderness at the implant site or other unusual symptoms.

The Johnson Law Firm, a national law firm representing a large number of patients who have been injured by the Bard Composix Kugel Hernia Mesh Patch, is providing recall information and claims evaluations at no cost to affected patients on their website at and toll free at 1-866-374-0338.


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