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BARTAL v. AstraZENECA PHARMACEUTICALS LP, 5:12-cv-02548 (PSG) RMW. (2012)

Court: District Court, N.D. California Number: infdco20120806481 Visitors: 4
Filed: Aug. 03, 2012
Latest Update: Aug. 03, 2012
Summary: ORDER GRANTING MOTION TO REMAND [Re Docket No. 16] RONALD M. WHYTE, District Judge. Plaintiffs move to remand this case to Santa Clara County Superior Court, arguing that the court lacks subject matter jurisdiction because of the absence of complete diversity of citizenship. Defendants AstraZeneca Pharmaceuticals LP and AstraZeneca LP (collectively "AstraZeneca") oppose the motion. Defendant McKesson Corporation ("McKesson") has not filed a response. For the reasons set forth below, the court
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ORDER GRANTING MOTION TO REMAND

[Re Docket No. 16]

RONALD M. WHYTE, District Judge.

Plaintiffs move to remand this case to Santa Clara County Superior Court, arguing that the court lacks subject matter jurisdiction because of the absence of complete diversity of citizenship. Defendants AstraZeneca Pharmaceuticals LP and AstraZeneca LP (collectively "AstraZeneca") oppose the motion. Defendant McKesson Corporation ("McKesson") has not filed a response. For the reasons set forth below, the court grants plaintiffs' motion to remand.

I. BACKGROUND

On April 17, 2012, plaintiffs commenced this action in Santa Clara County Superior Court, alleging state law causes of action against AstraZeneca and McKesson (collectively "defendants") for (1) strict products liability; (2) negligence; (3) breach of express warranty; (4) breach of implied warranty; (5) fraud; (6) fraudulent concealment; and (7) loss of consortium. Dkt. No. 1-1 (Compl.) ¶¶ 42-78. The six plaintiffs are residents of California, Arizona, Washington, and Puerto Rico. Id. ¶¶ 1-5. AstraZeneca is a Delaware corporation, with its principal place of business in that state. Id. ¶ 6. McKesson is also incorporated in Delaware, but has its principal place of business in California. Id. ¶ 7.

Plaintiffs' claims arise from their ingestion of Crestor, a cholesterol lowering medication manufactured by AstraZeneca and allegedly distributed by McKesson, which plaintiffs assert caused various serious health problems. Id. ¶¶ 14-17. Plaintiffs allege that, in addition to distribution, McKesson also participated in Crestor's marketing and promotion, intentionally and negligently misrepresenting the severity and scope of the drug's adverse effects. Id. ¶¶ 16-24; see also Dkt. No. 16 at 2:8-4:3.

AstraZeneca removed the action to this court on May 17, 2012, asserting diversity jurisdiction under 28 U.S.C. § 1332. Dkt. No. 1 ¶ 3. In its notice of remand, AstraZeneca conceded that McKesson is a California-based corporation, but contended that it was fraudulently joined. Accordingly, AstraZeneca maintains that there is complete diversity of citizenship and federal jurisdiction is proper. Id. ¶ 7.

II. ANALYSIS

A defendant can remove any civil action from state court if the federal courts would have original jurisdiction over the matter. 28 U.S.C. § 1441. However, "to protect the jurisdiction of state courts, removal jurisdiction is strictly construed in favor of remand." Harris v. Bankers Life and Cas. Co., 425 F.3d 689, 698 (9th Cir. 2005) (citing Shamrock Oil & Gas Corp. v. Sheets, 313 U.S. 100, 108-09 (1941)). Because "any doubt as to the right of removal must be resolved in favor of remand," Nasrawi v. Buck Consultants, LLC, 713 F.Supp.2d 1080, 1084 (E.D. Cal. 2010) (citing Gaus v. Miles, Inc., 980 F.2d 564, 566 (9th Cir. 1992)), if it appears a case was improperly removed, the district court is required to remand the action to state court. "This strong presumption against removal jurisdiction means that the defendant always has the burden of establishing that removal is proper." Id. (citation omitted).

When removal is based on diversity jurisdiction, as it is here, the court must exclude any fraudulently joined defendants from its determination of whether diversity exists. McCabe v. General Foods Corp., 811 F.2d 1336, 1339 (9th Cir. 1987). A defendant is fraudulently joined "[i]f the plaintiff fails to state a cause of action against [the] resident defendant, and the failure is obvious according to the settled rules of the state." Id. In the Ninth Circuit, failure to state a claim is "obvious" if, "after all disputed questions of fact and all ambiguities in the controlling state law are resolved in the plaintiff's favor, the plaintiff could not possibly recover against the party whose joinder is questioned." Nasrawi, 713 F. Supp. 2d at 1084-85 (citing Kruso v. Int'l Tel. & Tel. Corp., 872 F.2d 1416, 1426 (9th Cir. 1989)) (emphasis added).

AstraZeneca asserts that McKesson was fraudulently joined because plaintiffs rely solely on "`information and belief'" in alleging that McKesson distributed the Crestor they ingested. Dkt. No. 1 ¶ 15. AstraZeneca notes that thirty-five other entities also distributed Crestor during the time in question, and "plaintiffs provide no factual support for their implausible allegation that McKesson, one of these thirty-six distributors of Crestor, distributed the Crestor ingested by each and every one of the five personal injury Plaintiffs to this action." Id. ¶ 19. AstraZeneca concludes that, given the possibility that plaintiffs could have purchased Crestor from a distributor other than McKesson, McKesson is not a proper defendant.

However, plaintiffs allege that McKesson is "the largest pharmaceutical distributor in North America, distributing one-third of the medications used daily in North America." Compl. ¶ 7. Additionally, plaintiffs contend that McKesson is "fully injected into the marketing, distributing, testing, and patient-contacting aspects of the pharmaceutical world." Dkt. No. 16 at 2:8-9. While these assertions do not conclusively demonstrate that McKesson distributed the specific Crestor plaintiffs ingested or participated in the marketing or testing that ultimately caused plaintiffs' injury, AstraZeneca fails to provide any evidence that would unequivocally exclude these possibilities.1 As the court cannot conclude that it is "obvious" that plaintiffs will be unable to recover against McKesson, the court finds that McKesson is not fraudulently joined.

The court's conclusion is supported by the decisions of the federal courts in the Central, Eastern, and Southern Districts of California. Other plaintiffs in those districts filed identical claims against AstraZeneca and McKesson, and each court found that McKesson was not fraudulently joined and granted the plaintiffs' motions to remand. See Rivera v. AstraZeneca Pharmaceuticals LP, CV 12-02921 GAF JEMX, 2012 WL 2031348 (C.D. Cal. June 5, 2012); Mendez v. AstraZeneca Pharmaceuticals LP, 1-12-CV-00535-LJO, 2012 WL 1911382 (E.D. Cal. May 25, 2012); Norris v. AstraZeneca Pharmaceuticals LP, 12CV0836 JM BLM, 2012 WL 1944760 (S.D. Cal. May 30, 2012).

AstraZeneca also argues that, under Bockrath v. Aldrich Chem. Co., Inc., 21 Cal.4th 71, 81-83 (1999), because plaintiffs are uncertain of the identity of the distributor, they are required to name Doe defendants instead of asserting claims against McKesson on "information and belief." Dkt. No 1 ¶ 17. AstraZeneca reads Bockrath too broadly. The plaintiff in Bockrath brought an action against fifty-five defendants, claiming that the combined long-term exposure to these defendants' products caused him to develop cancer. Id. at 77. The California Supreme Court indicated that "if plaintiffs do not have a sufficient basis to allege that a particular internalized injury-causing toxin was manufactured or supplied by a specific person or entity, their complaints must name Doe defendants." Id. at 81 (citing Cal. Code Civ. Proc. § 474). However, the court went on to state that naming Doe defendants pursuant to section 474 was only appropriate if "plaintiff [was] ignorant of the identities of those who allegedly caused him to contract multiple myeloma." Id. at 83. The court explained that the purpose of section 474 was to protect plaintiffs "against the statute of limitations until they [could] identify the defendants and name them by their true names." Id. at 81.

Here, plaintiffs were fully aware of McKesson's identity and potential involvement from the outset and so had no need to avail themselves of the protection afforded by section 474. Further, given that plaintiffs allege that McKesson is the largest pharmaceutical distributor in North America and AstraZeneca does not offer any evidence that McKesson did not distribute the Crestor plaintiffs ingested, plaintiffs have a "sufficient basis" to name McKesson as a defendant. See Id. at 82 (defining a sufficient basis as a "well-founded belief" based on evidence that "has been or is likely to be found)"; see also Cal. Code Civ. Proc. § 128.7 (requiring that allegations in the pleading, "to the best of the person's knowledge, information, and belief. . . have evidentiary support or, if specifically so identified, are likely to have evidentiary support after a reasonable opportunity for further investigation or discovery"). In addition, plaintiffs contend that McKesson was involved in the marketing and promotion of Crestor and, therefore, is liable even if it did not distribute the particular Crestor plaintiffs took. Thus, it was proper for plaintiffs to join McKesson by name rather than as an additional Doe defendant.

III. ORDER

For the foregoing reasons, the court grants plaintiffs' motion to remand to Santa Clara County Superior Court.

IT IS SO ORDERED.

FootNotes


1. AstraZeneca notes that McKesson only distributed to Veterans Affairs hospitals in Puerto Rico (where plaintiff Rodriguez-Rivera is domiciled) and asserts that "there is no allegation that Ms. Rodriguez-Rivera obtained Crestor from a VA facility." Dkt. No 1 ¶ 20. However, AstraZeneca does not provide evidence showing that Ms. Rodriguez-Rivera did not obtain Crestor from a VA facility and, thus, fails to eliminate this possibility.
Source:  Leagle

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