In Re Avandia Marketing, Sales Practices & Products Liability Litigation

687 F. App'x 210
CourtCourt of Appeals for the Third Circuit
DecidedApril 19, 2017
Docket16-4161
StatusUnpublished
Cited by17 cases

This text of 687 F. App'x 210 (In Re Avandia Marketing, Sales Practices & Products Liability Litigation) is published on Counsel Stack Legal Research, covering Court of Appeals for the Third Circuit primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
In Re Avandia Marketing, Sales Practices & Products Liability Litigation, 687 F. App'x 210 (3d Cir. 2017).

Opinion

*212 OPINION *

PER CURIAM

The Mayfields appeal pro se from the District Court’s order dismissing their complaint with prejudice after they failed to comply with a pretrial discovery order. We will affirm.

I.

Rosie Mayfield died in 2012. According to her family, her death was attributable to complications traceable to long-term use of Avandia, an anti-diabetic medication manufactured by GlaxoSmithKline (GSK). When she died, she was part of a multi-plaintiff action against GSK in Missouri state court. In early 2015, Rosie’s spouse, ¿Tames, and their nine children—the Appellants here— opted but of a master settlement agreement in the Missouri action. The Missouri state court then granted GSK’s motion to dismiss that action in September 2015, citing the Mayfields’ failure to prosecute. Several months later, in March of 2015, the Mayfields filed a new Avandia-related negligence action against GSK in -the Superior Court of Arizona, Maricopa County. 1 GSK removed the action to the United States District Court for the District of Arizona based on diversity jurisdiction, and, on August 5, 2015, the Judicial Panel on Multidistrict Litigation transferred the case to the United States District Court for the Eastern District of Pennsylvania for pretrial proceedings as part of the Avandia Multidistrict Litigation (Avandia MDL), 2 finding that the “Mayfield Family action involves common questions of fact with actions previously transferred to MDL No. 1871.”

Meanwhile, on April 16, 2015, the District Judge in the Avandia MDL issued a pretrial order—which applied to “all cases that are originally filed in, transferred to, or removed to this Court and assigned to MDL 1871 on or after the date of this Order”—requiring that plaintiffs provide GSK an expert report 3 within 60 days of the date their action was transferred to the Avandia MDL. The order further provided that, if a plaintiff did not timely submit a report, GSK could send a deficiency notice, and then move to dismiss a complaint 14 days later if a plaintiff still had not filed a complying expert report.

On August 6, 2015, GSK sent the May-fields a letter accurately advising them that that their report would be due on October 5, 2015, but the Mayfields did not submit a report by that date. On October 13, 2015, GSK sent the Mayfields another letter stating that if they did not submit a report by October 27, 2015, it would move for dismissal. After Lawanda Mayfield contacted GSK, it permitted them to file their report by November 10, 2015, before moving for dismissal. Around that date, *213 James Mayfield submitted a letter to GSK and the District Judge, in which he appeared to suggest that Rosie’s medical records—-which apparently were in GSK’s possession—were sufficient to proceed in the litigation. 4 The Mayfields never filed a complying expert report, however.

GSK moved for dismissal under Federal Rule of Civil Procedure 37 on December 4, 2015, and, after the Mayfields failed to respond for almost a year, the District Judge dismissed their complaint with prejudice on October 19, 2016. A month later, Nicole Mayfield submitted a letter to the District Judge, stating that the Mayfields had attempted to obtain an expert report, but were unable to do so because they were proceeding pro se, and suggesting that they should be permitted to proceed to trial based on general existing medical knowledge about the dangers of Avandia. This timely appeal ensued.

II.

We have jurisdiction under 28 U.S.C. § 1291. We review, for abuse of discretion, the District Court’s dismissal of a complaint under Rule 37 for failure to comply with pretrial discovery orders, see Curtis T. Bedwell & Sons, Inc. v. Int’l Fid. Ins. Co., 843 F.2d 683, 691 (3d Cir. 1988), based on the factors set out in Poulis v. State Farm Fire & Cas. Co., 747 F.2d 863, 868-70 (3d Cir. 1984), which are: (1) the extent of the party’s personal responsibility; (2) prejudice to the adversary; (3) a history of dilatoriness; (4) whether the conduct of the party was willful or in bad faith; (5) the effectiveness of sanctions other than dismissal; and (6) the meritoriousness of the claim or defense. Not all factors need to be satisfied for the District Court to dismiss a complaint, and while we recognize that the sanction of dismissal is extreme and should be reserved for cases where it is “justly merited,” our standard of review is deferential. Ware v. Rodale Press, Inc., 322 F.3d 218, 221-22 (3d Cir. 2003).

The District Court explicitly addressed four factors in dismissing the Mayfields’ complaint: (1) that the Mayfields were personally responsible for their non-compliance; (2) that the non-compliance “reflected] an intentional disregard for the Court’s instructions”; (3) that GSK was prejudiced by the delay arising from noncompliance; and (4) that no other, lesser sanctions would have been effective. The Mayfields do not directly argue that the District Court inappropriately applied the Poulis factors; instead they argue that (1) they were unable to obtain a complying expert report, despite having attempted to do so; (2) Rosie’s medical records, GSK’s previous settlement offer in the Missouri action, and other existing general medical knowledge concerning the dangers of Avandia constituted sufficient proof to proceed to trial; and (3) the District Court’s pretrial order did not apply to them because they initially filed their action in Arizona state court in March 2015. None of these arguments persuades us that the District Court abused its discretion in dismissing their complaint. 5

First, the District Judge’s April 16, 2016, order—which applied to all cases transferred to the Avandia MDL after that *214 date—plainly applied to the Mayfields’ action, which was transferred to the Avandia MDL in August 2015. The Mayfields appear to argue that, because they filed their action in state court before the District Judge issued the order, it did not apply to them. This argument simply misreads—or overlooks—the unambiguous language of the order.

As to their remaining arguments, we have recognized that multidistrict litigation “presents a special situation, in which the district judge must be given wide latitude with regard to case management in order to effectively achieve the goals set forth by the legislation that created the Judicial Panel on Multidistrict Litigation.” In re Asbestos Prod. Liab.

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Bluebook (online)
687 F. App'x 210, Counsel Stack Legal Research, https://law.counselstack.com/opinion/in-re-avandia-marketing-sales-practices-products-liability-litigation-ca3-2017.