Bard Hernia Mesh Recall. Here are some of the hernia mesh recalls since 2005: 2005 Hernia Mesh Implant Recalls. Bard is headquartered in Rhode Island, many hernia mesh lawsuits have been filed in Rhode Island state court. Ethicon Proceed Surgical Mesh was recalled. A Bard Perfix Plug lawsuit alleges that the hernia mesh cut off the flow of blood and sperm to and from a man's testicles after it migrated out of position, resulting in the need for revision surgery. In December 2016, that plaintiff had to go through revision surgery, however, to have the Bard Mesh PerFix Plug removed. Bard’s Ventralex mesh, Perfix plug and Composix Kugel mesh are the hernia mesh products most commonly at issue in these lawsuits. Bard ® Mesh can be tailored preoperatively and customized to any unique situation. Bard ® Mesh reinforces the weakened area, allowing for tissue ingrowth and resiliency. Recall Status 1: Terminated 3 on June 06, 2016: Recall Number: Z-1649-2010: Recall Event ID: 54884: Product Classification: Mesh, surgical, polymeric - Product Code FTL: Product: Bard Mesh Monofilament Knitted Polypropylene; size 3" x 6", 3 units per box. Bard was, at all times relevant hereto, responsible for the actions of Davol and ... PerFix Plug, Cat No. 0112760, Lot No. Case 6:18-cv-03019-DPR Document 1 Filed 01/18/18 Page 3 of 34. An FDA Class 1 recall is the most urgent type of recall. Bard and other mesh products are Class II medical devices which were approved through the FDA’s 510(k) process. With more than 50 years of clinical experience, Bard ® Mesh is the Gold Standard product to be used in a "tension-free" hernia repair technique. Atrium's C-QUR, certain devices from C.R. Approximately 8,000 cases are pending against Bard in Rhode Island state court. This process “fast tracks” a product to market by giving quick approval to medical products when the company … Because C.R. 2013 Hernia Mesh Implant Recalls. 4 13. There have been recalls for these Bard hernia mesh devices. R. Bard and Davol recalled Composix Kugel mesh products from the market starting in 2005. The recall, issued by the Food and Drug Administration (FDA) was a Class 1 recall, the highest level of … 5. The Gold Standard, Monofilament, Polypropylene Mesh. Physiomesh isn't the only hernia mesh product with a number of adverse event reports. It was implanted to fix a right inguinal hernia. Bard, Inc. 100 Sockanossett Crossroad Cranston, RI 02920. The plaintiff in this lawsuit says that a May 2014 procedure was when he first encountered the Bard PerFix Plug. Bard.They are used to treat inguinal hernias.However, both devices suffer from many of the same problems that plague other hernia mesh products. Bard Mesh PerFix Plug. 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