MDL Mass Tort & Class Action Monitor
Developed to serve primarily as a litigation scouting report for plaintiff and defense counsel, insurers and legal service providers, HarrisMartin’s MDL Mass Tort & Class Action Monitor covers significant new filings and decisions in the JPML, MDL and related mass tort arenas. The quick delivery of breaking news and additional features will keep you within close range of every development occurring in the high-stakes environment of mass torts litigation — where minutes can make a difference. The MDL Mass Tort & Class Action Monitor is an online-only offering that includes frequent email updates and is available at no charge to annual and event sponsors of HarrisMartin’s CLE Conferences.
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Issue #3, February 2017
Howmedica Opposes Motion to Create LFIT V40 MDL Docket, Says ‘Small Number of Actions’ Doesn’t Justify Coordination
Howmedica Osteonics Corp. has opposed a motion to create a coordinated pretrial docket for claims relating to the defendant’s LFIT V40 femoral head, saying that only a handful of cases are implicated in the motion and “only a fraction of those involves products subject” to the recall cited by the plaintiffs.
Plaintiffs with claims relating to Stryker’s LFIT Anatomic Cobalt Chromium V40 femoral heads have sought multi-county litigation designation in the state of New Jersey, saying the cases will involve “recurrent legal issues of design defect, failure to warn, breach of warranty and possibly manufacturing defect.”
A coordinated federal docket will be established in New York for lawsuits targeting the makers of Eliquis, a so-called “breakthrough” anticoagulant that plaintiffs say can cause life-threatening and irreversible bleeding.
Plaintiffs with claims against makers of the Type 2 diabetes drug Farxiga have asked the U.S. Judicial Panel on Multidistrict Litigation to create a centralized docket for their cases, just months after they were excluded from the creation of an Invokana MDL.
Noting that several considerations “fatally undercut the case for centralization,” the Judicial Panel on Multidistrict Litigation denied a petition to consolidate federal lawsuits alleging that proton pump inhibitors (PPI) cause kidney disease.
Plaintiffs have moved to establish a consolidated docket for more than 30 federal lawsuits alleging injury caused by a metal-on-metal hip implant system manufactured by Smith & Nephew.
Issue #2, January 2017
A petition has been filed seeking to establish a centralized MDL docket for more than a dozen pending lawsuits by heart surgery patients who claim they developed serious post-surgical infections caused by bacteria dispersed from the Sorin 3T Heater-Cooler System.
Plaintiffs have asked the JPML to create a multidistrict litigation docket for claims relating to Stryker’s recalled LFIT V40 femoral head, saying that transfer and consolidation for pre-trial proceedings will “promote the just and efficient conduct of these actions.”
Issue #001, December 2016
A petition was filed late Thursday urging the Judicial Panel on Mutlidistrict Litigation (JPML) to create a centralized docket for more than 100 lawsuits filed by women who claim they developed intracranial hypertension as a result of their use of Bayer’s Mirena birth control device.
A Kentucky woman has sued Takeda Pharmaceuticals USA Inc. in Illinois federal court, claiming that the company’s heartburn drug Dexilant is to blame for her development of chronic kidney disease.