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