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Judge allows users of non-recalled hernia patches to file lawsuits
Thursday, 31 January 2008
A Federal judge has ruled that patients who used a Composix Kugel mesh hernia patch not specifically recalled by the manufacturer can still file a hernia patch lawsuit. The ruling by U.S. District Court Judge Mary Lisi also transferred all federal lawsuits against Davol Inc.—the manufacturer of the Kugel hernia patch—to Rhode Island.
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Federal judicial panel announces transfer of Kugel lawsuits
Wednesday, 05 September 2007
A federal judicial panel has announced that all of the hernia patch lawsuits filed over the Composix Kugel mesh hernia patch will be transferred to Rhode Island for pre-trial proceedings.
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FDA says Davol waited too long to issue hernia patch recall
Saturday, 24 March 2007
The manufacturer of the Composix Kugel mesh patch kept the device on the market long after it learned of several injuries linked with the hernia patch, including at least one fatality, according to an FDA report.
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More criticism of Davol’s slow response in hernia patch recall
Thursday, 15 March 2007
The slow response of C.R. Bard, Inc. to injuries suffered by Composix Kugel mesh hernia patch patients is the subject of criticism in a NY Times article.
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FDA updates hernia patch recall to Class 1
Thursday, 01 February 2007

The Food and Drug Administration has announced that it is updating the recall on large sized versions of the Bard Composix Kugel Mesh hernia patch to a Class 1 recall. Davol Inc.—the manufacturer of the Kugel hernia patch—has issued three separate hernia patch recalls since December 2005 due to reports that the device could break after it is implanted, leading to serious and potentially deadly hernia patch side effects.

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