Yesterday, the Supreme Court issued its ruling in the much-anticipated Mutual Pharms. Co. v. Bartlett, No. 12-142 (on appeal from the First Circuit Bartlett v. Mutual Pharms. Co., 678 F.3d 30 (1st Cir. 2012)). As we predicted, the Court reversed the First Circuit’s decision and held that “[s]tate-law design defect claims that turn on the adequacy of a drug’s warnings are pre-empted by federal law under PLIVA.”
BARTLETT’S BACKGROUND -
Bartlett’s facts are undeniably tragic. The plaintiff, Karen Bartlett, took generic sulindac (manufactured by Mutual) for shoulder pain. She developed Stevens-Johnson syndrome/toxic epidermal necrolysis (SJS/TEN) and suffered permanent injury and disfigurement. By the time of trial, the only remaining claim for the jury to decide was whether sulindac was defectively designed. The jury found in Bartlett’s favor and awarded her $21.06 million in compensatory damages.
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Topics: Design Defects, Generic Drugs, Mutual Pharmaceuticals v Bartlett, Preemption, Prescription Drugs, SCOTUS, Warning Labels
Published In: Civil Procedure Updates, Conflict of Laws Updates, Products Liability Updates, Science, Computers & Technology Updates
DISCLAIMER: Because of the generality of this update, the information provided herein may not be applicable in all situations and should not be acted upon without specific legal advice based on particular situations.
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