The Kugel mesh hernia patch is used to repair ventral hernias. There are over 750,000 hernia operations each year in the U.S. The Kugel hernia mesh patch is manufactured by C.R. Bard, Inc., and their subsidiary, Davol, Inc. who owns the patent on the device. The Kugel mesh patch is made of two pieces of mesh that surround a flexible plastic ring. The surgeon places the mesh patch in a small incision. The surgeon would fold the patch and place it at the site of the hernia. The released ring would then spring back into its original shape, flattening the patch. The meshlike material would serve as a substrate, allowing the hernia patient’s own tissue to grow and assist in healing the hernia.
The Kugel Mesh Patch can break, however, leading to bowel perforations and chronic intestinal fistulae. These are very serious conditions that pose a significant health risk to Kugel hernia patch patients. The problem with the Kugel hernia patch is that the plastic component could break and cut through a patient’s internal organs and tissue. The FDA has received reports of more than 80 injuries and other problems possibly related to it, including several fatalities. Our Kugel hernia patch lawyers expect an increasing number of reports of injuries in the weeks and months to come.
In late 2005, C.R. Bard sent out a recall on the Kugel patch, urging doctors to stop using some versions of the product, because a plastic component could break and cut through a patient’s internal organs and tissue. Our Kugel patch lawyers believe that, at least by this time, C.R. Bard knew, or should have known, that other lots and versions were also implicated, both because of the evidence available to them, and because all of the Kugel patches had the same or similar memory recoil ring, which was causing the defect in the Kugel patches. Accordingly, our Kugel mesh hernia patch lawyers expect that more, if not all, of the patches will eventually be recalled.
Since December, there have been three separate recalls of different models of the Kugel patch. The FDA says surgeons and hospitals should immediately stop using the recalled patches and return the unused patches to the company. Patients who have been implanted with one of the recalled Kugel devices should consult their doctor or surgeon. You should seek immediate medical attention if you are experiencing persistent and/or unexplained abdominal pain, fever, tenderness or any painful lumps or bulges at the site of the Kugel implant/surgery, or any other unusual symptoms.
Our lawyers are currently reviewing Kugel mesh hernia patch cases throughout the United States and Canada. If you have one of these implanted devices, you may be entitled to compensation. Call our Kugel mesh hernia patch lawyers at 1-800-553-8082 click here for a free web consultation.