2010 Hernia Mesh Implant Recalls. Bard’s Ventralex mesh, Perfix plug and Composix Kugel mesh are the hernia mesh products most commonly at issue in these lawsuits. Approximately 8,000 cases are pending against Bard in Rhode Island state court. Bard like the PerFix and 3DMax devices, and some devices from Covidien like the Parietex ProGrip have all been the subjects of many such reports. Physiomesh isn't the only hernia mesh product with a number of adverse event reports. The Gold Standard, Monofilament, Polypropylene Mesh. 4 13. Because C.R. Atrium's C-QUR, certain devices from C.R. The recall, issued by the Food and Drug Administration (FDA) was a Class 1 recall, the highest level of … Bard and other mesh products are Class II medical devices which were approved through the FDA’s 510(k) process. This process “fast tracks” a product to market by giving quick approval to medical products when the company … Bard ® Mesh can be tailored preoperatively and customized to any unique situation. Bard ® Mesh reinforces the weakened area, allowing for tissue ingrowth and resiliency. Bard Mesh PerFix Plug. An FDA Class 1 recall is the most urgent type of recall. 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. Bard.They are used to treat inguinal hernias.However, both devices suffer from many of the same problems that plague other hernia mesh products. HUXF0920 was implanted in Plaintiff during this repair. Bard Hernia Mesh FDA Warnings and Recalls. Bard was, at all times relevant hereto, responsible for the actions of Davol and ... PerFix Plug, Cat No. The Bard PerFix Plug and the Bard PerFix Light Plug are implantable hernia mesh devices that were made by C.R. 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 is headquartered in Rhode Island, many hernia mesh lawsuits have been filed in Rhode Island state court. Davol Inc. A Subsidiary of C.R. Bard was subject to recalls for Composix Kugel mesh products due to safety concerns about the plastic which would splinter and migrate away from the surgical site. Here are some of the hernia mesh recalls since 2005: 2005 Hernia Mesh Implant Recalls. C.R. The plaintiff in this lawsuit says that a May 2014 procedure was when he first encountered the Bard PerFix Plug. It was implanted to fix a right inguinal hernia. 2013 Hernia Mesh Implant Recalls. There have been recalls for these Bard hernia mesh devices. Case 6:18-cv-03019-DPR Document 1 Filed 01/18/18 Page 3 of 34. 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