Prempro Products Liability Litigation v. Wyeth

591 F.3d 613, 65 A.L.R. Fed. 2d 747, 2010 U.S. App. LEXIS 239, 2010 WL 21090
CourtCourt of Appeals for the Eighth Circuit
DecidedJanuary 6, 2010
Docket09-1205, 09-1250, 09-1373
StatusPublished
Cited by322 cases

This text of 591 F.3d 613 (Prempro Products Liability Litigation v. Wyeth) is published on Counsel Stack Legal Research, covering Court of Appeals for the Eighth Circuit primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Prempro Products Liability Litigation v. Wyeth, 591 F.3d 613, 65 A.L.R. Fed. 2d 747, 2010 U.S. App. LEXIS 239, 2010 WL 21090 (8th Cir. 2010).

Opinion

BRIGHT, Circuit Judge.

The plaintiffs, women and next-of-kin of deceased women, sued a number of manufacturers of hormone replacement therapy drugs, asserting the drugs caused breast cancer. The defendants, manufacturers of hormone replacement therapy drugs (“manufacturers”), removed the cases to federal court. The plaintiffs moved to remand to state court on the grounds that complete diversity of citizenship was lacking, thereby depriving the court of subject matter jurisdiction. The district court concluded that the plaintiffs’ claims were misjoined to defeat diversity jurisdiction, dropped the non-diverse plaintiffs, and dismissed these cases. Plaintiffs appeal, and we reverse the district court’s orders denying plaintiffs’ motions to remand and granting the manufacturers’ motions to dismiss duplicative cases.

I. BACKGROUND

A. Hormone Replacement Therapy

Hormone replacement therapy (“HRT”) drugs are used in the treatment of menopausal symptoms. Such symptoms include hot flashes, chills, headache, irritability, and vaginal atrophy. HRT drugs consist of a combination of estrogen and progestin. The Women’s Health Initiative (WHI), a group focused on defining the risks and benefits of strategies that could reduce heart disease, cancer, and fractures in post-menopausal women, began studying the effects of HRT drugs in the 1990s. The WHI enrolled 161,809 post-menopau *617 sal women between 50 and 79 years of age into a set of clinical trials.

WHI studied the effect of estrogen plus progestin in 16,608 women with an intact uterus. Women were either assigned a daily dose of estrogen plus progestin or a placebo. In 2002, an independent data and safety monitoring board revealed that the number of cases of breast cancer in the estrogen plus progestin group had crossed the boundary established as a signal of increased risk. The independent board recommended that the trial be ended early based on an increased breast cancer risk. The results of the WHI study were published in The Journal of the American Medical Association. See Risks and Benefits of Estrogen Plus Progestin in Healthy Postmenopausal Women, 288 J. Am. Med. Ass’n. 321-33 (2002), available at http:// jama.ama-assn.org/cgi/content/full/288/3/ 321.

B. The Lawsuits

This case concerns three lawsuits. The Kirkland suit was brought by 57 women who each alleged injuries resulting from their use of HRT medications. The Kirkland plaintiffs alleged they each developed breast cancer after taking HRT drugs that were manufactured, marketed, and sold by one or more of eleven manufacturers. Fourteen Kirkland plaintiffs are citizens of the same state as at least one of the manufacturers. Three of those fourteen plaintiffs asserted claims against manufacturers with the same citizenship. For example, Nancy States is a citizen of Pennsylvania, the same state as Wyeth Pharmaceuticals, Inc., a company that manufactured and marketed HRT drugs she took.

The Jasperson suit was brought by Rick Jasperson, as trustee of the next-of-kin of six decedents who used HRT drugs. The Jasperson plaintiffs alleged that in each case, the next-of-kin sustained injuries when a woman family member developed breast cancer as a result of taking HRT drugs that were manufactured, marketed, and sold by one or more of six defendants. One of the six decedents, Elizabeth Mendelson, was a citizen-of New Jersey, the same state as Pharmacia Corporation, Wyeth, and Pharmacia & Upjohn Company, companies that manufactured and marketed HRT drugs that Mendelson took.

The Allen suit was brought by 60 women who also alleged they each developed breast cancer as a result of HRT medications manufactured, marketed, and sold by one or more of eight defendants. Five Allen plaintiffs are citizens of the same state as at least one of the defendants. Three of these five plaintiffs asserted claims against manufacturers who were citizens of the same state. For example, Rachel Epstein is a citizen of New York, the same state as Pfizer, a company that manufactured and marketed HRT drugs that she took.

C. Procedural History

The Kirkland, Jasperson, and Allen plaintiffs filed suits for damages in Minnesota state court in July 2008. In each of the three consolidated cases, the plaintiffs alleged they or a decedent family member had developed breast cancer from taking HRT medications. The plaintiffs asserted state law claims for negligence, strict liability, breach of implied warranty, breach of express warranty, fraud, negligent misrepresentation, and statutory violations of the False and Misleading Advertising Act, the Prevention of Consumer Fraud Act, and the Uniform Deceptive Trade Practices Act.

The manufacturers removed all three cases to the United States District Court for the District of Minnesota. In the manufacturers’ removal petitions, they argued *618 diversity jurisdiction existed under the fraudulent misjoinder doctrine. They alleged that the plaintiffs joined their claims together against the manufacturers to defeat diversity jurisdiction. The manufacturers argued that the plaintiffs’ claims were fraudulently misjoined, stating that those claims did not arise out of the same transaction or occurrence, a requirement for joinder under Federal Rule of Civil Procedure 20(a).

The plaintiffs filed motions to remand the cases to state court for lack of subject matter jurisdiction, asserting that complete diversity between the plaintiffs and defendants did not exist. Before the plaintiffs’ motions were addressed, the litigation came before the United States Judicial Panel on Multidistrict Litigation (“MDL”). The Kirkland and Jasperson cases were transferred to the Eastern District of Arkansas and assigned to an MDL judge. Plaintiffs requested that the MDL court rule on their pending motions to remand to state court.

Before the MDL court ruled on the question of remand, on December 19, 2008, the manufacturers moved to dismiss most of the claims brought by the Kirkland plaintiffs and all of the claims brought on behalf of the Jasperson decedents on the grounds that the plaintiffs’ claims were duplicative of earlier filed California claims. 1 Plaintiffs’ oppositions to the motions were due on December 30, 2008, and they requested an extension of time to reply to the manufacturers’ motions to dismiss.

On December 29, 2008, the court denied plaintiffs’ requests for an extension, stating that it “did not grant your Motion for Extension of Time to Respond, because Pm satisfied that you couldn’t say anything that would change my mind on the issues involved here.” On that same day, the court denied in part plaintiffs’ motions to remand the Kirkland and Jasperson cases to state court, concluding that the plaintiffs were misjoined.

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Bluebook (online)
591 F.3d 613, 65 A.L.R. Fed. 2d 747, 2010 U.S. App. LEXIS 239, 2010 WL 21090, Counsel Stack Legal Research, https://law.counselstack.com/opinion/prempro-products-liability-litigation-v-wyeth-ca8-2010.