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    Products Liability Law Legal Research Blog

    PRODUCTS LIABILITY: Educational Warnings Regarding Drug Discussed in the Context of Removal

    Posted by Gale Burns on Tue, Apr 26, 2011 @ 13:04 PM

    April 26, 2011

    Jeremy Taylor, Senior Attorney, National Legal Research Group

    A recent decision by a U.S. District Court in Pennsylvania combined, in an interesting way, the issues of removal of a case to federal court and of the potential responsibility under a products liability theory of the publisher of an "education monograph" containing warnings about a prescription drug.  See Slater v. Hoffman-La Roche, Inc., Civ. Action No. 10-6956, 2011 WL 1087240, at *1 (E.D. Pa. Mar. 24, 2011).  The plaintiff sued the manufacturer of the acne drug Accutane, alleging that the drug had caused him to develop colitis and ulcerative colitis.  The plaintiff also sued the publisher of a monograph explaining the dangers of Accutane.  The plaintiff was a resident of Wisconsin, the drug manufacturer was a resident of New Jersey, and the publisher of the educational monograph was a Delaware corporation with its principal place of business in Pennsylvania.  Following the plaintiff's filing in Pennsylvania state court, the defendants removed the action to the federal district court.  The plaintiff moved to remand the case to the state court.  The court noted that unless the publisher had been fraudulently joined, the claims against it had to be remanded, in light of the rule that removal to federal court is permissible only if none of the parties in interest properly joined and served as defendants is a citizen of the state in which the action has been brought.  See 28 U.S.C. § 1441(b).

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    Topics: legal research, products liability, Slater v. Hoffman-La Roche, removal, fraudulent joinder, remand, 28 U.S.C. § 1441, intermediary doctrine, monograph publisher

    PRODUCTS LIABILITY: U.S. District Court Upholds Award of $21 Million Against Manufacturer of Anti-Inflammatory Drug

    Posted by Gale Burns on Mon, Jan 17, 2011 @ 12:01 PM

    January 18, 2011

    Jeremy Taylor, Senior Attorney, National Legal Research Group

    A recent decision by the U.S. District Court for the District of New Hampshire addressed a number of issues regarding defective design of an anti-inflammatory drug, in upholding a jury verdict of over $21 million in favor of the plaintiff.  See Bartlett v. Mut. Pharm. Co., Civ. No. 08‑cv‑358‑JL, 2011 DNH 004 (D.N.H. Jan. 5, 2011).  The plaintiff alleged that her use of the defendant's drug "sulindac" had caused her to suffer severe and permanent injuries, including blindness.  Specifically, the plaintiff had contracted Stevens-Johnson Syndrome ("SJS"), progressing to toxic epidermal necrolysis ("TEN"), as a result of her use of sulindac.  The plaintiff asserted claims of strict liability for defective design, strict liability for failure to warn, fraud, and negligence under state law.  The district court granted the manufacturer's motion for summary judgment on all but the plaintiff's defective design claim, which was the sole cause of action proceeding to trial.  The jury found in the plaintiff's favor and awarded her $21.06 million in compensatory damages, including $16.5 million for pain and suffering.  Following the verdict, the defendant manufacturer renewed its motion for judgment as a matter of law under Federal Rule of Civil Procedure 50(b), arguing that there was insufficient evidence to support the plaintiff's claim.

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    Topics: legal research, products liability, defective design, Mutual Pharmaceuticals Company, compensatory damages, risk/benefit test

    PRODUCTS LIABILITY: Exception in State Statute Providing Defense Based upon FDA Approval of Labeling Not Preempted

    Posted by Gale Burns on Fri, Jan 7, 2011 @ 15:01 PM

    November 9, 2010

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    Topics: legal research, products liability, Jeremy Taylor, federal preemption, FDCA, conflict with state tort law, defense to liability

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