In Re Blood Reagents Antitrust Litigation

783 F.3d 183, 91 Fed. R. Serv. 3d 693, 2015 U.S. App. LEXIS 5630, 2015 WL 1543101
CourtCourt of Appeals for the Third Circuit
DecidedApril 8, 2015
Docket12-4067
StatusPublished
Cited by77 cases

This text of 783 F.3d 183 (In Re Blood Reagents Antitrust 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 Blood Reagents Antitrust Litigation, 783 F.3d 183, 91 Fed. R. Serv. 3d 693, 2015 U.S. App. LEXIS 5630, 2015 WL 1543101 (3d Cir. 2015).

Opinion

OPINION OF THE COURT

SCIRICA, Circuit Judge.

The principal issues in this appeal under Federal Rule of Civil Procedure 23(f) in this antitrust action are (1) whether Rule 23 requires scrutiny under Daubert v. Merrell Dow Pharmaceuticals, Inc., 509 U.S. 579, 113 S.Ct. 2786, 125 L.Ed.2d 469 (1993), of challenged expert testimony and (2) the propriety of class certification in light of the Supreme Court’s decision in Comcast Corp. v. Behrend, - U.S. -, 133 S.Ct. 1426, 185 L.Ed.2d 515 (2013) (Comcast), which re *185 versed Behrend v. Comcast Corp., 655 F.3d 182 (3d Cir.2011) {Behrend), after the District Court relied on Behrend in granting class certification. Because we find that the District Court had no opportunity to consider the implications of Com-cast and hold that, if applicable, a court must resolve any Daubert challenges to expert testimony offered to demonstrate conformity with Rule 23, we vacate and remand. 1

I. 2

Plaintiffs are direct purchasers of traditional blood reagents, products used to test blood compatibility between donors and recipients, from two companies, defendants Immucor, Inc., which has settled with plaintiffs, and Ortho-Clinical Diagnostics, Inc., the appellant here. Plaintiffs claim Ortho and Immucor violated federal antitrust law by conspiring to fix traditional blood reagent prices.

By 1999, the entire domestic supply of traditional blood reagents had come under the control of Ortho and Immucor in a duopoly in which both companies anticipated they could raise their prices and increase their profits. 3 In November 2000, Ortho and Immucor executives attended an annual trade meeting at which plaintiffs assert the conspiracy began. Soon thereafter, both Ortho and Immucor began increasing traditional blood reagents prices in rapid succession, and by 2009, many prices had risen more than 2000%. Following a Department of Justice probe, a number of private suits were filed and transferred by the Judicial Panel on Multidistrict Litigation to the District Court, which consolidated them in December 2009.

Plaintiffs seek damages under the Clayton Act, see 15 U.S.C. § 15, for alleged horizontal price fixing in violation of the Sherman Act, see 15 U.S.C. § 1. In July 2012, after preliminary approval of plaintiffs’ settlement with Immucor, the court-held a hearing to determine whether to certify plaintiffs’ class of “[a]ll individuals and entities who purchased traditional blood reagents in the United States directly from Defendants Immucor, Inc., and Ortho-Clinical Diagnostics, Inc. at any time from January 1, 2000 through the present.” 283 F.R.D. at 247. The court then certified the class over Ortho’s objection. We granted Ortho’s petition to appeal under Rule 23(f).

II.

Plaintiffs relied in part on expert testimony to produce their antitrust impact analyses and damages models. The District Court evaluated the testimony, the reliability of which Ortho consistently chal *186 lenged, and, in part by holding that the testimony “could evolve to become admissible evidence” at trial, determined that plaintiffs had met Rule 23(b)(3)’s predominance requirement. See 283 F.R.D. at 243-45 (quoting Behrend, 655 F.3d at 204 n. 13). Relying on our decision in Behrend, the court rejected Ortho’s challenges to plaintiffs’ damages models as irrelevant to class certification because, the court reasoned,

[vjirtually all of Ortho’s arguments go to the merits of the models [plaintiffs’ expert] has constructed: the question whether the models give rise to “a just and reasonable inference or [are] speculative.” Behrend, 655 F.3d at 206. These merits questions have some force, and they may prove persuasive at the summary judgment stage. However, they do not overlap with the Rule 23 requirements, because they neither implicate a need for individual proof nor convince the Court that [the] models could not “evolve to become admissible evidence.” Id. at 204 n. 13.

Blood Reagents, 283 F.R.D. at 240-41 (third alteration in original).

On appeal, Ortho contends the trial court failed to rigorously scrutinize whether “questions of law or fact common to class members predominate over any questions affecting only individual members.” Fed.R.Civ.P. 23(b)(3). In particular, pointing to Comcast, Ortho asserts the trial court erred by declining to address at class certification whether plaintiffs’ damages models were capable of producing just and reasonable damage estimates at trial and by accepting plaintiffs’ theory as capable of proving classwide antitrust impact: 4 Or-tho also argues that, under the class certification standard, the trial court should have scrutinized the plaintiffs’ expert’s testimony under Daubert.

III.

A.

Because the District Court did not have the opportunity to consider Corn-cast’s later-issued guidance in the first instance, we will vacate the class certification order and remand for reconsideration. Without foreclosing what other conclusions the District Court might reach regarding Comcast’s ramifications for antitrust damages models 5 or proving antitrust impact, 6 we believe Behrend’s “could evolve” formulation of the Rule 23 standard did not survive Comcast. See Comcast, 133 S.Ct. at 1433 (criticizing Behrend for “finding it *187 unnecessary to decide “whether the [expert’s damages] methodology [was] a just and reasonable inference or speculative’ ” and indicating that such a methodology is not “acceptable so long as it can be applied classwide, no matter how arbitrary the measurements may be” (second alteration in original) (quoting Behrend, 655 F.3d at 206)). As we stated in In re Hydrogen Peroxide Antitrust Litigation,

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Bluebook (online)
783 F.3d 183, 91 Fed. R. Serv. 3d 693, 2015 U.S. App. LEXIS 5630, 2015 WL 1543101, Counsel Stack Legal Research, https://law.counselstack.com/opinion/in-re-blood-reagents-antitrust-litigation-ca3-2015.