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Shareholders have sued the maker of a surgical robot claiming the company has “grossly underreported” injuries and deaths attributed to the da Vinci. The 67-page shareholder derivative complaint was filed by the city of Birmingham and Alabama’s Relief and Retirement System naming Intuitive Surgical of Sunnyvale, California, the maker of […]
Search Results: hip implant
Two years ago, the Food and Drug Association (FDA) was still uncertain about how to address growing concerns over the effects of metal-on-metal (MoM) hip implants. So, on June 27, 2012, the FDA’s Orthopaedic and Rehabilitation Devices Panel convened an Advisory Committee in order to hear experts and the public […]
This blog is a continuation of “The FDA’s MoM Panel” which you should read first in order to have a clear idea of what happened at this important event. Click here to go back to Part I. The Manufacturers All major manufacturers still selling MoM hip implants were invited to […]
The start of 2014 has seen some very significant developments in the national Biomet metal-on-metal hip implant litigation. Perhaps the most significant development though is Biomet’s offering, and the court’s acceptance, of a settlement for claimants who have undergone revision surgeries. On February 3, 2014, Judge Miller entered an order […]
This blog is a continuation of our “Metal Testing: New FDA Guidelines” which you should read first if you want more information on how to test for metal artifacts in your hip. Metal Ions Metal ions are different from metal artifacts. They are microscopic, so you cannot see them with […]
The U.S. Food and Drug Administration (FDA) is considered by many to be the premier safety and health regulator in the world. The agency oversees about one-quarter of all products Americans consume including food, drugs and medical devices. Most Americans assume they are safe with the FDA at the helm. […]
Three years ago, Public Citizen issued a report that documents all of the settlements between pharmaceutical giants and the federal and state governments due to violations such as overcharging patients or by off-label marketing. At the time the tally was about $20 billion covering a period of 20 years. The […]
The Food and Drug Administration (FDA) finally seems to be taking something other than a head-in-the-sand approach to monitoring medical devices after they are approved and in use by patients. The U.S. does not monitor medical devices after they go through the FDA’s approval process. Since most medical devices are […]
This is just the latest in a series of recalls for healthcare giant Johnson & Johnson (J&J). This week, the company recalled about 200,000 bottles of concentrated Motrin Infant drops Original Berry Flavor. The company’s McNeil unit made the decision after tiny particles of plastic were found in some bottles […]
The national litigation efforts in state and federal court involving Wright Medical’s defective metal-on-metal hip implant products ( Conserve®,Dynasty®, Profemur® and the Lineage®) have been proceeding well over the past few months with additional progress expected through the end of 2013. The coordinated litigation efforts in both the federal Multi-District Litigation (MDL) […]
