In re BLOOD REAGENTS ANTITRUST LITIGATION.
Ortho Clinical Diagnostics, Inc., Appellant.
No. 12-4067.
United States Court of Appeals, Third Circuit.
Argued: Feb. 12, 2014. Filed: April 8, 2015.
183-189
IV.
For the reasons set forth above, we will reverse the District Court‘s order dismissing Kaymark‘s
Richard E. Coe, Esq., Joanne C. Lewers, Esq., Chanda A. Miller, Esq., Paul H. Saint-Antoine, Esq., [Argued] Drinker, Biddle & Reath, Philadelphia, PA, for Appellant.
Before: SMITH, CHAGARES, and SCIRICA, Circuit Judges.
OPINION OF THE COURT
SCIRICA, Circuit Judge.
The principal issues in this appeal under
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
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
[v]irtually 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.”
III.
A.
Because the District Court did not have the opportunity to consider Comcast‘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 models5 or proving antitrust impact,6 we believe Behrend‘s “could evolve” formulation of the
B.
We join certain of our sister courts to hold that a plaintiff cannot rely on challenged expert testimony, when critical to class certification, to demonstrate conformity with
In the District Court, plaintiffs relied on expert testimony to produce most of their antitrust impact analyses and damages models, which they offered to demonstrate that common questions predominated over individual questions as required by
Because Ortho consistently challenged the reliability of plaintiffs’ expert‘s methodologies and the sufficiency of his testimony to satisfy
IV.
For the foregoing reasons, we will vacate the class certification order and remand for proceedings consistent with this opinion.
SCIRICA, Circuit Judge.
