Incubadora Mexicana, SA de CV v. Zoetis, Inc.

116 F. Supp. 3d 519, 2015 U.S. Dist. LEXIS 100103, 2015 WL 4598031
CourtDistrict Court, E.D. Pennsylvania
DecidedJuly 31, 2015
DocketCivil Action No. 15-216
StatusPublished
Cited by8 cases

This text of 116 F. Supp. 3d 519 (Incubadora Mexicana, SA de CV v. Zoetis, Inc.) 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
Incubadora Mexicana, SA de CV v. Zoetis, Inc., 116 F. Supp. 3d 519, 2015 U.S. Dist. LEXIS 100103, 2015 WL 4598031 (E.D. Pa. 2015).

Opinion

[522]*522 OPINION

WENDY BEETLESTONE, District Judge.

I. INTRODUCTION

Plaintiffs are Mexican chicken breeders who have sued two American pharmaceutical companies, Defendant Zoetis Inc. and Defendant Pfizer Inc., for claims based upon Defendants’ alleged manufacture, sale, and distribution of a defective poultry vaccine, “Poulvac,” which failed to prevent Plaintiffs’ livestock from becoming infected with the deadly Marek virus. Before the Court is Defendant Zoetis, Inc.’s motion to dismiss on the grounds of forum non con-veniens.1 Zoetis asserts that the doctrine of forum non conveniens mandates dismissal because Mexico provides an adequate alternative forum for this dispute and the relevant interests weigh in favor of trial there. For the reasons set forth below, the motion shall be denied.

II. BACKGROUND

Plaintiff Incubadora Mexicana, SA de CV (“IMSA”) is a Mexican company, with corporate quarters in Puebla, Mexico. Am. Compl. ¶ 3. Plaintiff Incubadoras Ran-cho Grande S.A. de C.V. (“Rancho Grande”) is also a Mexican company, with corporate headquarters in Sonora, Mexico. Id. ¶ 5. Both IMSA and Rancho Grande breed and supply egg-laying chickens. Id. ¶¶4, 6. Rancho Grande also distributes chicken eggs. Id. ¶ 6.

Defendant Pfizer, Inc. (“Pfizer”) is an international pharmaceutical company with corporate headquarters in New York, New York. Id. ¶8. In 1952, Defendant Pfizer created a dedicated animal health division for the development, manufacture and distribution of animal health pharmaceuticals. Id. ¶ 9. The North American headquarters for Pfizer’s Animal Health Division was located in Exton, Pennsylvania with a distribution warehouse located in Lewisberry, Pennsylvania. Id. ¶ 10. In 2002, Pfizer announced the formation of Zoetis, Inc. (“Zoetis”), which was to replace Pfizer’s Animal Health Division and operate as an independent company. Id. ¶ 12. In June 2013, Zoetis moved its global headquarters from Pennsylvania to Florham Park, New Jersey and completed its corporate separation from Pfizer. Id. ¶ 13. Zoetis operates in four regions, including Mexico. Id. ¶ 15.

As part of their business, Plaintiffs routinely purchase a vaccine to protect their chickens from the Marek virus, which is often fatal to young chicks if not properly treated. Id. ¶27. Since at least 2007, Plaintiffs have purchased Defendants’ Poulvac vaccine, which Defendants advertised as the “most effective [Marek vaccine] on the market.” Id. ¶¶ 33-36. The shipment of the vaccines was controlled and supervised through a series of agents and couriers, all of whom Plaintiffs allege were selected and hired by Defendants. Id. ¶ 21. To effectuate sales to customers in Mexico, Defendants transferred title of the vaccine to a Belgian subsidiary. Id. ¶ 21(d). They transferred possession of the vaccine from the manufacturing plant to a customs agent, who brought the product through Mexican customs before turning it over to a Mexican “logistical services provider.” Id. The logistical service provider then shipped the product, via courier, to regional sales representatives, who delivered the product to customers, including Plaintiffs. Id.

As a result of Plaintiffs’ commercial relationship with Defendants, Plaintiffs “enjoyed a highly successful vaccination program in their poultry business, which resulted in very low rates of Marek’s disease and in turn high yields of commercial eggs.” Id. ¶ 40. In the summer [523]*523of 2013 through the spring of 2014, Plaintiffs once again placed orders for Poulvac through Defendant Zoetis’ sales and marketing staff. Id. ¶41. In January 2014, Defendants determined that the vaccine lots that had been shipped to Plaintiffs and other breeders in Mexico were defective because they had been improperly stored and/or transported. Id. ¶47. In response, Defendants Zoetis and Pfizer coordinated an effort to investigate, test, and manage potential claims arising out of the business losses from the defective vaccine lots. Id. ¶ 50.

Defendants did not notify Plaintiffs of the defect in their vaccine until July 31, 2014, more than seven months after they became aware of the vaccine’s,ineffectiveness. Id. ¶ 59. Meanwhile, Plaintiffs continued to administer vaccine from the defective lots. Id. ¶ 51. As a result, Plaintiffs began to experience significant loss of poultry livestock. Id. ¶ 53, Plaintiffs suffered further losses when their customers also began to experience significant livestock losses or diminished production capacity because the chickens they had purchased from Plaintiffs were treated with the defective vaccine. Id. ¶ 57.

Plaintiffs attempted to contact the local Zoetis region affiliate to address the issue but were told by the head of the poultry unit at Zoetis Mexico that his branch had no authority and that Zoetis’ corporate headquarters in New Jersey was handling the matter. Id. ¶¶ 55-56. In response to Plaintiffs’ complaints, Zoetis suggested that the parties meet in January 2015 at the International Production and Processing Expo (IPPE) in Atlanta to try to resolve Plaintiffs’ claims. Id. ¶63. Plaintiffs sent representatives to Atlanta, where they met with Zoetis’ U.S.-based in-house counsel for Latin America and Zoetis’ U.S.-based Director of Global Poultry as well as the head of the poultry unit at Zoetis Mexico. Id. ¶64. During that meeting, the Zoetis personnel reiterated that the matter had to be addressed and decided by corporate officers in the United States. Id. ¶ 65.

III. LEGAL STANDARD

Under the doctrine of forum non conveniens, a district court may exercise its discretion to dismiss a case where: (1) an alternative forum has jurisdiction to hear the case; and (2) when trial in the plaintiffs chosen forum “would establish oppressiveness and vexation to a defendant out of all proportion to the plaintiffs convenience,” or when the Plaintiffs chosen forum is inappropriate due to the court’s own administrative and legal problems. Eurofins Pharma U.S. Holdings v. BioAlliance Pharma SA, 623 F.3d 147, 160 (3d Cir.2010) (citing Windt v. Qwest Commc’ns Int’l, Inc., 529 F.3d 183, 189 (3d Cir.2008)).

The first step when considering a motion to dismiss on forum non conveniens grounds is to determine whether an adequate alternate forum exists. Id. at 160 (citing Windt, 529 F.3d at 189-90). If an adequate alternate forum exists, the district court must then determine the amount of deference to give the plaintiffs choice of forum. Id. (citing Windt, 529 F.3d at 190). Finally, the district court must then determine if the chosen forum would result in oppression or vexation to the defendant out of all proportion to the plaintiffs convenience. Id. In undertaking this final analysis, the Court considers the private interest factors affecting the convenience of the litigants and public interest factors affecting the convenience of the forum. Windt, 529 F.3d at 189 (citing Gulf Oil Corp. v. Gilbert,

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Bluebook (online)
116 F. Supp. 3d 519, 2015 U.S. Dist. LEXIS 100103, 2015 WL 4598031, Counsel Stack Legal Research, https://law.counselstack.com/opinion/incubadora-mexicana-sa-de-cv-v-zoetis-inc-paed-2015.