Hernia Patch Recall | Beasley Allen On December 22, 2005, the FDA and Davol/Bard notified healthcare professionals of a class 1 recall of the Bard Composix Kugel Mesh hernia patch (X-Large Patch Oval with ePTFE). Since this time, the hernia patch recall has twice been expanded by the FDA and Davol. Patients who have who have been implanted with one of the recalled hernia patches should seek medical attention immediately if they experience symptoms that could be associated with hernia patch failure such as: fever; unexplained or persistent abdominal pain; tenderness at the implant site; other unusual symptoms. Herniapatchrecall.org~Site InfoWhoisTrace RouteRBL Check
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