Physiomesh isn't the only hernia mesh product with a number of adverse event reports. 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. Case 6:18-cv-03019-DPR Document 1 Filed 01/18/18 Page 3 of 34. Bard is headquartered in Rhode Island, many hernia mesh lawsuits have been filed in Rhode Island state court. An FDA Class 1 recall is the most urgent type of recall. R. Bard and Davol recalled Composix Kugel mesh products from the market starting in 2005. 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. 5. 2010 Hernia Mesh Implant Recalls. The plaintiff in this lawsuit says that a May 2014 procedure was when he first encountered the Bard PerFix Plug. 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. 0112760, Lot No. Ethicon Proceed Surgical Mesh was recalled. Davol Inc. A Subsidiary of C.R. There have been recalls for these Bard hernia mesh devices. Atrium's C-QUR, certain devices from C.R. 4 13. Bard’s Ventralex mesh, Perfix plug and Composix Kugel mesh are the hernia mesh products most commonly at issue in these lawsuits. This process “fast tracks” a product to market by giving quick approval to medical products when the company … Approximately 8,000 cases are pending against Bard in Rhode Island state court. Bard.They are used to treat inguinal hernias.However, both devices suffer from many of the same problems that plague other hernia mesh products. C.R. 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. Bard was, at all times relevant hereto, responsible for the actions of Davol and ... PerFix Plug, Cat No. Because C.R. Bard, Inc. 100 Sockanossett Crossroad Cranston, RI 02920. The recall, issued by the Food and Drug Administration (FDA) was a Class 1 recall, the highest level of … Bard Mesh PerFix Plug. In December 2016, that plaintiff had to go through revision surgery, however, to have the Bard Mesh PerFix Plug removed. 2013 Hernia Mesh Implant Recalls. Bard ® Mesh can be tailored preoperatively and customized to any unique situation. The Bard PerFix Plug and the Bard PerFix Light Plug are implantable hernia mesh devices that were made by C.R. HUXF0920 was implanted in Plaintiff during this repair. Bard and other mesh products are Class II medical devices which were approved through the FDA’s 510(k) process. 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