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product_liability composix-kugelThe Composix Kugel Mesh Patch, a device used in the repair of ventral hernias, was first recalled in December 2005 because of dangerous product defects. According to the U.S. Food and Drug Administration, defective Composix patches could create fistulas – abnormal passages between organs – and also cause organ punctures. Unfortunately, thousands of Americans have been implanted with these potentially defective patches.
If you or a loved one has suffered serious injury because of a defective Composix Kugel Mesh Patch, you may be entitled to damages. Please contact us today for a complimentary consultation with an expert personal injury lawyer who can answer your questions and help you plan a course of action.
Symptoms of a Defective Composix Kugel Mesh Patch
Symptoms of organ punctures or fistulas caused by a defective Composix Kugel Mesh Patch may include:
Individuals using the Kugel patch and experiencing any of these or other symptoms should consult with a physician immediately.
Recalled Patches
Bard, the maker of these patches, expanded the initial recall in March 2006 to include additional products and lot numbers. The patches affected by the product recalls include the following:
Injured by a Defective Composix Kugel Mesh Patch?
If you''ve been harmed by the Composix Kugel Mesh Patch, please contact us to speak with a highly skilled and qualified personal injury attorney FREE of charge. You may be able to recover compensation for your medical expenses, pain, suffering, and more.
Late in 2005, C.R.Bard Inc. issued a recall of the composix hernia patch , which is manufactured by its subsidiary, Davol Inc. The recall urged doctors to stop using the larger i...