Kugel Mesh Hernia Patch Lawsuit

Medical device makers develop and market products that are supposed to help health care consumers. In each case, manufacturers are expected and required to conduct testing to determine the effectiveness and safety of their product. While the Food and Drug Administration (FDA) is responsible for approving drugs and medical devices, the FDA is not a consumer group or safety watchdog. In fact, the FDA often depends on manufacturers to provide them with proof of product safety. Over the years, however, drug manufacturers and medical device makers have sometimes chosen to place profits above quality control and public safety. At The Potts Law Firm, our attorneys work with medical professionals, researchers, design engineers and other experts in exposing dangers and design flaws inherent in certain drugs and medical devices.

The medical device lawyers at the Potts Law Firm have a successful track record of trying complex medical cases and getting justice for our clients. When it is in the best interests of our clients, our lawyers combine our firm’s resources and abilities with those of other law firms to obtain the best outcomes for individuals or groups of clients.

Dangerous Drugs and Defective Medical Devices

Defective medical devices and dangerous drug cases have included:

Kugel Mesh Hernia Patch Bellweather Jury Trial

Mr. Potts was co-counsel with Don Migliori of Motley Rice and Jeffrey Kuntz in the first Kugel Mesh Hernia Patch bellwether case tried in the country as part of the federal multi district litigation. Mr. Potts handled key witnesses at trial including the plaintiffs’ chief liability expert witness, a bioengineer. After a 4 week jury trial, the 9 person jury unanimously found that the Composix Kugel Hernia Patch which was placed in over 100,000 patients was defective and unreasonably dangerous due to its propensity to change shape and buckle in the body.

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