Recall Status 1: Terminated 3 on May 02, 2012 Date Initiated by Firm: DecemRecall Number: Z-0935-2009 Date Posted: JanuRecall Status 1: Terminated 3 on May 02, 2012ĭate Initiated by Firm: December 08, 2008 Recall Event ID: 50479: 510(K)Number: K792281 Product Classification: Surgical mesh - Product Code FTL: Product: Bard 3D Max Mesh, Left large, Sterile Pre-formed Knitted Polypropylene Product.Class 3 Device Recall Bard/Davol fda.gov.The Bard 3dMax mesh is made with Polypropylene, a plastic … However, the number of complications, side effects, and injuries being reported across the country continue to grow. Bard 3D Max Recall - Hernia Mesh Lawsuit Ĭurrently, there is no FDA recall for the Bard 3D Max mesh.It is designated in two orientations - "Right" and "Left" for use to the right or left side of the human body. What is 3D Max mesh?īard 3D Max Mesh is an anatomically shaped pre-formed polypropylene mesh indicated for use in the repair of hernias and chest wall defects.
Below you will find a mesh lawsuit update pertaining to Bard/ Davol mesh. Many people are unaware of Bard’s checkered past in which Bard plead guilty in 1993 to 391 felonies and three Bard executives were sentenced to 18 months in jail. Others are researching whether there has been a Marlex mesh recall. When first released, the Bard 3DMax was constructed with full weight polypropylene fibers. Is there an FDA recall for the Bard 3D Max mesh?Ĭurrently, there is no FDA recall for the Bard 3D Max mesh. 3D Max is a hernia mesh medical device utilized by surgeons as treatment for inguinal hernias. Bard and Bard’s corporate subsidiary, Davol, have manufactured 3DMax mesh since circa 2007. There are currently hundreds of of 3Dmax hernia mesh lawsuits pending in Federal and State Courts.