Law360 (January 11, 2021, 8:52 PM EST) — A Florida federal choose presiding over sprawling multidistrict litigation involving the carcinogens discovered within the heartburn treatment Zantac minimize extra claims on Friday from the litigation, holding that design defect claims are barred by federal regulation.
U.S. District Decide Robin L. Rosenberg stated that state design defect claims towards name-brand Zantac producers, like Pfizer Inc. and Sanofi-Aventis U.S. LLC, are preempted by the Federal Meals Drug and Beauty Act as a result of it was inconceivable for the businesses to vary the drug’s formulation with out the approval of the U.S. Meals and Drug Administration.
The choose rejected arguments by customers and third-party payers that…
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