In April 2017, the Judicial Panel on Multi-district Litigation issued an order consolidating all Stryker LFIT V40 cases filed in federal court before a single judge in Massachusetts. The purpose of this consolidation is to provide oversight and assistance by the Court in conducting complex national discovery in a coordinated manner for all parties. This... Continue Reading →
Femoral Head Implant Recall: Stryker Orthopaedics
To read the original recall from Stryker Orthopaedics regarding the LFIT Anatomic CoCr V40 Femoral Heads manufactured between January 1, 2002 and March 4, 2011, please Click Here.
FDA wants to inform you about complications that may occur with the surgical mesh that is sometimes used to repair hernias, and to provide you with questions you may want to ask your surgeon before having this procedure. Read More...
FDA Safety Communication: Surgical Mesh
The reputation of Roundup, whose active ingredient is the world’s most widely used weed killer, took a hit on Tuesday when a federal court unsealed documents raising questions about its safety and the research practices of its manufacturer, the chemical giant Monsanto.