In re Blood Reagents Antitrust Litigation

266 F. Supp. 3d 750
CourtDistrict Court, E.D. Pennsylvania
DecidedJuly 19, 2017
DocketMDL NO. 2081; MASTER FILE NO. 09-MD-2081
StatusPublished
Cited by3 cases

This text of 266 F. Supp. 3d 750 (In re Blood Reagents Antitrust Litigation) is published on Counsel Stack Legal Research, covering District Court, E.D. Pennsylvania 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, 266 F. Supp. 3d 750 (E.D. Pa. 2017).

Opinion

[754]*754MEMORANDUM

DuBois, District Judge

TABLE OF CONTENTS

I. INTRODUCTION... 754

II. BACKGROUND... 754

A. Factual Background... 755

B. Creation of a Duopoly.. .756

C. 2001 Price Increase... 756

1. Shift to Blood Bank Leadership Program ...757

2. Aleged Price-Fixing Conspiracy. . .757

D. 2005 Price Increases... 759

1. Price Increases... 759

2. 2004 GPO Contract Cancellations ...762

E. 2008 Price Increase... 762

F. Evidentiary Issues... 764

1. Parties’ Statements... 764

2. Co-Conspirator Statements... 764

III. Procedural History.. .764

IV. Applicable Law.. .766

A. The Matsushita Standard... 766

B. Analyzing Evidence at the Summary Judgment Stage.. .768

V. Discussion... 768

A. Per Se Standard — Rule of Reason Standard...769

B. Parallel Conduct — 2005 and 2008 Price Increases.. .769

C. Motive to Enter, into Conspiracy. . .772

D. Actions Contrary to Interest.. .772

E. Pretextual Explanations... 774

F. Evidence Implying a Traditional Conspiracy.. .775

1. 2001 Price Increase... 775

2. 2005 Price Increase... 778

3. 2008 Price Increase.,. 782

G. “Plus Factors” — Conclusion... 783

H. Fraudulent Concealment.. .784

I. Applicable Law.. .784

2. Discussion.. .784

a. Awareness of Facts Supporting Claim... 784

b. Reasonable Diligence... 786

VI.Conclusion.. .787

I. INTRODUCTION

In this multidistrict litigation consolidating thirty-three separate civil antitrust actions, plaintiffs, purchasers of traditional blood reagents (“TBRs”) allege that defendants, the two leading producers of blood reagents — Ortho-Clinical Diagnostics, Inc. (“Ortho”) and Immucor, Inc. (“Immu-cor”) — conspired to unreasonably restrain trade and commerce in violation of § 1 of the Sherman Antitrust Act, 15 U.S.C. § 1. In September 2012, plaintiffs and Immucor reached a settlement. Ortho is the sole remaining defendant. Presently before the Court is Ortho’s Motion for Summary Judgment. For the reasons that follow, the Court denies in part and grants in part Ortho’s Motion.

II. BACKGROUND

Between 2000 and 2009, Ortho and Im-mucor drastically increased the prices of [755]*755their blood reagent products — some product prices increased 20 fold. Resp. to Mot. for Summ. J., Ex. 1, Corrected Rep. of John C. Beyer, Ph.D. Regarding Liability and Damages (“Beyer Aug. Rep.”), Aug. 14, 2012, ¶ 28. The parties agree that some part of this increase resulted from the elimination of all firms in the blood reagents market except .for Ortho and Immu-cor by 1999, and the resulting market power of those two firms. However, plaintiffs allege that an unlawful horizontal price-fixing agreement between Ortho and Im-mucor, beginning in November 2000, resulting in more than $650 million in market overcharges to plaintiffs and class members.

A. Factual Background

Blood reagents are used to identify properties of human blood. Most large purchasers of blood reagents are blood donor centers and hospitals, which use them to test whether the blood of a potential donor is compatible with the blood of a potential recipient. Mot. for Summ. J, Ex. 15, Report of Teresa Harris (“Harris Rep.”), ¶¶ 6-8. Under applicable Food and Drug Administration (“FDA”) regulations, Blood Bank and Transfusion Standards promulgated by the American Association of Blood Banks (“AABB”), and other rules, blood donor centers must test a donor’s ABO group (blood classification based on the inherited properties of red blood cells) and Rh type and perform an antibody screen each time he or she donates. Harris Rep. ¶ 20. Hospitals must conduct similar tests on a recipient before providing a blood transfusion. Id. ¶ 7.

There are two basic categories of blood reagents: traditional and automated. Although Ortho and Immucor sold products in both categories throughout the class period, the class in this case includes only purchasers of TBRs. When using TBRs, laboratory technicians test blood manually in test tubes and interpret the results. Id. ¶ 14. “Automated” or “proprietary” blood reagents (“ABRs”), on the other hand, are often used with specialized equipment. Id. ABRs allow for quicker testing while requiring less skill and decreasing the risk of technician error but tend to be more expensive than TBRs. Resp., Ex. 27, Declaration of Bill Weiss (“Weiss Deck”), ¶ 14.

From 2000 to 2010, Ortho and Immucor each sold more than forty different TBR products. Harris Rep. Ex. C. A list provided by plaintiffs’ industry expert, Teresa Harris, shows that most Ortho TBR products had an equivalent Immucor TBR product, and vice versa. Id. Harris opines that, while some ¿re nonidentical pairs, the nonidentical pairs “perform exactly the same function.” Resp., Ex. 11, Reply Report of Teresa Harris' (“Harris Reply”) Ex. B, ¶ 8.

For much of the period between 2000 and 2009, Ortho and Immucor remained the sole producers of TBRs because the market was difficult to enter. New entrants into the TBR market faced a prolonged FDA licensing process. Resp., Ex. 21, Declaration of Mike Poynter (“Poynter Decl.”), ¶ 26. Ed Gallup, the Chief Executive of Immucor from 1982 until 2003,1 addressed what he believed to be the significant barriers to entry in a 2002 interview with The Wall Street Transcript. SOF ¶¶ 117-19. In regard to potential competition, Gallup stated that “[i]t took the last company that applied six years to receive a FDA establishment license in this industry” and branded FDA licensing as a “fairly large barrier to entry.” SOF ¶ 119. Similarly,, John Kingsbury, Director of Sales and Marketing for Ortho from [756]*7561996 through 1999, testified that FDA regulations made Ortho’s blood bank business, including TBRs, “more complex to operate in, more time consuming, more costly, etc.” Pis. SOF ¶ 51. In 2008, two new TBR producers, Alba Bioscience, and Biotest, overcame those barriers and joined Ortho and Immucor in the market. SOF ¶¶ 565-70.

B. Creation of a Duopoly

In the 1980s and 1990s, the TBR industry was highly competitive. Pis. SOF ¶ 24. In the fifteen to twenty years prior to 2003, there were as many as fourteen competitors in the market. Pis. SOF ¶ 27. As a result, prices steadily decreased and profitability diminished. Pis. SOF ¶ 24.

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