The Biomet MDL (multidistrict litigation) was established for the organization and litigation of individual personal injury lawsuits against Biomet in the fall of 2012. In February of this year, the MDL contained 132 individual lawsuits. The count now stands upwards of 180 individual lawsuits, and it is still growing every […]
Category: Mass Tort News
Nexium – its effective marketing directly to consumers reminds Americans it is the “little purple pill” designed to treat acid reflux disease. Nexium, manufactured by AstraZeneca, is a proton pump inhibitor (PPI) prescribed to treat heartburn, acid-reflux, and inflammation of the esophagus. But plaintiffs allege that Nexium may cause a […]
You might not realize that K-Y Jelly is a medical device but it is and the U.S. Food and Drug Administration (FDA) is not happy about claims made by Johnson & Johnson concerning the personal lubricant. As a result McNeil Consumer Healthcare, a subsidiary of J&J, has recalled 2.3 million […]
It is a popular antibiotic often asked for because it can be taken with fewer doses over a shorter period of time. Now the U.S. Food and Drug Administration (FDA) says azithromycin (Zithromax) has been linked to an irregular heart rhythm that can be fatal in some patients. Medical researchers […]
This report is confusing to the many people who know from experience that taking the anticoagulant Pradaxa (dabigatran) is more dangerous than warfarin (Coumadin), the treatment that’s been the standard of care for decades. According to a published perspective in the online March 14, New England Journal of Medicine (NEJM), […]
With about 10,000 metal hip lawsuits filed around the country, jury selection in the second trial involving the DePuy ASR (Articular Surface Replacement) hip is underway in Cook County, Illinois with opening statements to begin mid-month. Meanwhile the jury is considering the evidence presented in Los Angeles Superior Court in […]
Last month, the U.S. Food and Drug Administration issued a Safety Communication to set some general guidelines for physicians and patients who have metal-on-metal (MoM) hip implants. Last month the agency also issued a proposed order that would require MoM hip manufacturers to submit premarket approval (PMA) applications before […]
Apparently, the FDA will expedite its abbreviated 510K approval process. The medical device industry is painting this as an improvement in the device approval process, but at what cost? And, for who is this expedited clearance process an improvement? According to an analysis from the medical device consulting company Emergo […]
An MDL (multidistrict litigation) was established for the prosecution of individual personal injury lawsuits against Biomet in the fall of 2012. The Judicial Panel on Multidistrict Litigation (JPML) heard attorney arguments on September 20, 2012, at a hearing in New York City. The plaintiffs requested consolidation of the pending lawsuits […]
A Florida grandmother has filed a complaint against the maker of the antidepressant Zoloft over a birth injury suffered by her grandchild. The lawsuit was filed November 28, 2012 in federal court in the Northern District of Florida, which is in Pensacola. According to the complaint against drug maker Pfizer […]
