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872 F. Supp. 2d 162
D. Conn.
2012
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Background

  • Diversity-based products liability action involving combination hormone therapy drugs Premarin and Prempro alleged to cause breast cancer.
  • Plaintiff sues Wyeth for eleven counts, including strict liability design defect (Count II) and failure to warn among others.
  • Court previously granted summary judgment on breach of express warranty and CUTPA and partial on alternative design theory; remaining counts treated as a single CPLA claim.
  • Wyeth argues Connecticut does not recognize strict liability design-defect claims for prescription drugs under the CPLA, citing Restatement § 402A cmt. (k).
  • Judge issues memorandum predicting how CT Supreme Court would interpret comment k and how design-warranty/warning claims should be litigated at trial.
  • Key conclusion: CT would apply comment k as a case-by-case affirmative defense to design defects; warning defects remain governed by § 52-572q.

Issues

Issue Plaintiff's Argument Defendant's Argument Held
Does Connecticut recognize design-defect strict liability for prescription drugs? Moss contends CT recognizes design defect claims under CPLA. Wyeth argues comment k provides blanket immunity for all prescription drugs. CT would adopt case-by-case defense under comment k.
How does comment k apply to prescription drug design defects? Design defect claims survive unless proven unavoidably unsafe with warnings. Comment k bars recovery for unavoidably unsafe drugs with proper warnings and manufacturing. Comment k applied as affirmative defense on a case-by-case basis.
What is the scope of warning defect liability for prescription drugs under CT law? 52-572q imposes strict liability for inadequate warnings. Warnings doctrine interacts with negligence principles; warnings can be adequate or inadequate. Warning defects assessed under § 52-572q; foreseeability and knowledge limit warnings.
Is the learned intermediary doctrine relevant to design defect and warning claims? Learned intermediary doctrine affects warnings analysis under CT law. Doctrine supports physician as intermediary; does not immunize design defects. Learned intermediary doctrine partially informs design-warnings analysis; not a shield for design defects.

Key Cases Cited

  • Vitanza v. Upjohn Co., 257 Conn. 365, 778 A.2d 829 (2001) (Conn. 2001) (adopts learned intermediary doctrine; discusses comment k context)
  • Potter v. Chicago Pneumatic Tool Co., 241 Conn. 199, 694 A.2d 1319 (1997) (Conn. 1997) (defines strict liability tests and consumer expectations)
  • Hill v. Searle Laboratories, 884 F.2d 1064 (8th Cir. 1989) (case-by-case view of comment k; affirmative defense approach)
  • Basko v. Sterling Drug, Inc., 416 F.2d 417 (2d Cir. 1969) (rejects blanket strict liability immunity; warns on design defects)
  • Castrignano v. E.R. Squibb & Sons, Inc., 546 A.2d 775 (R.I. 1988) (comment k applied in broader prescription drug context)
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Case Details

Case Name: Moss v. Wyeth Inc.
Court Name: District Court, D. Connecticut
Date Published: May 24, 2012
Citations: 872 F. Supp. 2d 162; 2012 WL 1899876; 2012 U.S. Dist. LEXIS 72569; No. 3:04cv1511 (SRU)
Docket Number: No. 3:04cv1511 (SRU)
Court Abbreviation: D. Conn.
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