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