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Hernia Patch Litigation Court Will Hear Claims by Patients With Non-Recalled Hernia Mesh and Patch Devices Manufactured by Bard, Inc. and Davol, Inc. Over the last few years a number of patients have brought hernia mesh patch lawsuits against C.R. Bard, Inc., and Davol, Inc. alleging that their hernia mesh patch devices were defective and caused injuries. Many the claims were brought after an FDA hernia patch recall including claims based on defects in hernia mesh patches non-recalled hernia mesh patch devices. In a recent ruling the court clarified the scope of the consolidated proceedings to include both recalled and non-recalled devices. Hernia patch lawsuits from across the United States have now been consolidated into a single court for http://www.avvo.com/attorneys/90010-ca-leodis-matthews-297315.html all pretrial proceedings. The court assigned to oversee the nationwide hernia patch and mesh lawsuits will hear claims of patients with both recalled and non-recalled hernia mesh and patch devices. The federal Multi-District Litigation court has announced that it will hear hernia mesh and patch lawsuits involving both recalled and non-recalled devices manufactured by C.R.