Beasley, Allen, Crow, Methvin, Portis & Miles, P.C.

With the constant advancements in medical practices and technology, it is sometimes easy for medical professionals to become too confident in their abilities and overlook the underlying facts that are in front of them. This degree of confidence may have been the case for the recall on the Kugel hernia patch made by Davol, a subsidiary of C.R. Bard Inc., which now is paying for its apparent lack of concern over product safety.

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We live in a time when ultramodern technology permeates every aspect of our lives at blistering speeds. Nearly every day we hear of yet another advancement that promises to better our lives in some way. Medicine and medical technologies, such as the Kugel Mesh Patch used to treat hernias, stand on the forefront of medicine’s quantum push forward. Manufactured by Devol, Inc., the Kugel Mesh Patch consists of a circle or oval of mesh that is surrounded by a plastic ring. The device is engineered and folded so that it may be surgically inserted into a small incision. Once in place, the patch unfolds and expands and the abdominal wall is reinforced.

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How do makers of implanted medical devices react when one of their products starts breaking?

One answer can be found in the case of a hernia repair device made by a subsidiary of C. R. Bard Inc. In late 2005, the company sent out a recall, 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.

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