Heart Valve Plaintiff Can Sue For Failure To Report Adverse Events To FDA

(October 3, 2018, 10:26 AM EDT) -- NEW YORK — A New York federal judge on Sept. 28 dismissed all claims in a defective heart valve products liability case except one that the defendants failed to report adverse events to the Food and Drug Administration (A.F., et al. v. Sorin Group USA, Inc., et al., No. 17-5903, S.D. N.Y., 2018 U.S. Dist. LEXIS 168726)....

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