In re Zoloft (Sertraline Hydrochloride) Products Liability Litigation

257 F. Supp. 3d 717
District Court, E.D. Pennsylvania·Decided June 20, 2017·No. MDL NO. 2342 12-MD-2342; Civil Action No. 16-1438·Published·Cited by 3 cases

Opinion

[718] MEMORANDUM OPINION

Rufe, District Judge.

Plaintiffs brought suit against Pfizer, Inc., Pfizer International LLC, J.B. Roerig & Co. and Greenstone LLC (collectively, “Pfizer”) and McKesson Inc., alleging numerous state-law claims, including failure to warn, negligence, and fraudulent concealment. Plaintiffs filed the action in California state court, Defendants removed it to federal court on the basis of diversity jurisdiction, and the case was transferred to this Court as part of the Zoloft Multidis-trict Litigation (“MDL”).

Plaintiffs have moved to remand the matter to California state court for lack of diversity jurisdiction, as Plaintiffs are California citizens and Defendant McKesson is a California corporation. Defendants argue that the lone California defendant, McKes-son, is fraudulently joined and therefore complete diversity exists between the parties. This Court has considered the issue before, in both the Avandia and Zoloft MDLs. Consistent with those earlier decisions, the Court holds that Plaintiffs have pled sufficient facts to assert a claim against McKesson,1 but that the history of the Zoloft litigation shows that Plaintiffs have no real intention to pursue claims against McKesson, such that McKesson was fraudulently joined.2 Therefore, Plaintiffs’ motion to remand will be denied.

I. BACKGROUND

Plaintiff D.B. was born in 2014 with a serious birth defect allegedly caused by Zoloft taken during pregnancy by his mother, Plaintiff Julie Parmley.3 Plaintiffs allege Defendants aggressively marketed and sold Zoloft to pregnant women despite evidence that Zoloft increased the risk for birth defects, without informing doctors or consumers of these risks.4 The only specific allegations related to McKesson state that McKesson is a Delaware corporation headquartered in California, and “at all times relevant hereto, Defendant McKes-son was engaged in the business of researching, designing, developing, licensing, compounding, testing, producing, manufacturing, assembling, processing, packaging, inspecting, labeling, supplying, distributing, selling and/or warranting Zoloft.... Plaintiffs are informed and believe Defendant McKesson distributed the Zoloft that was dispensed to [Parmley].”5 Plaintiffs also allege that, according to Pfizer’s website, McKesson was the single largest distributor of Pfizer’s pharmaceutical products.6

II. LEGAL STANDARD

Removal of a civil action from state to federal court is governed by 28 U.S.C. § 1441. The removal statutes “are to be [719] strictly construed against removal and all doubts should be resolved in favor of remand.” 7 The party removing the case has the burden to prove that federal jurisdiction is proper at all stages of the litigation.8 As is relevant here, Defendants may only “remove an action on the basis of diversity of citizenship if there is complete diversity between all named plaintiffs and all named defendants, and no defendant is a citizen of the forum State.”9

III. DISCUSSION

Plaintiffs argue that remand is proper because there is incomplete diversity between the Plaintiffs and all named Defendants.10 Defendants argue that McKesson is fraudulently joined and therefore should not be considered in any diversity jurisdiction analysis and that, without McKesson, diversity jurisdiction is properly invoked. Defendants therefore seek to “establish that the non-diverse defendant!;] [was] ‘fraudulently named or joined solely to defeat diversity jurisdiction.” 11

In order to establish fraudulent joinder, a defendant must prove that “there is no reasonable basis in fact or colorable ground supporting the claim against the joined defendant, or no real intention in good faith to prosecute the action against the defendants or seek a joint judgment.”12 A claim is colorable if it is not “wholly insubstantial and frivolous” in light of the relevant law.13 With respect to a claim’s factual basis, a “limited piercing of the allegations to discover fraudulent joinder” may be appropriate.14 The limitation is significant, however, with the permissible inquiry being, less probing than the review a district court conducts in deciding a motion to dismiss for failure to state a claim under Federal Rule of Civil Procedure 12(b)(6).15 Moreover, “if there is even a possibility that a state court would find that the complaint states a cause of action against any one of the resident defendants, the federal court must find that joinder was proper and remand the case to state court.”16 A plaintiffs alleged failure to adequately plead a viable cause of action against a defendant must be “obvious according to the settled rules of the state.”17 The heavy burden of demonstrating that a defendant was fraudulently joined rests with the defendant making the charge.18 When evaluating a charge of fraudulent joinder, the “district court must’ resolve all [720] contested issues of substantive fact” and “any uncertainties as to the current state of controlling substantive law in favor of the plaintiff.”19

Defendants first argue that Plaintiffs’ Complaint lacks specific allegations necessary to assert a claim against McKesson. The Court has explored, and rejected, this argument in the Avandia MDL, which included numerous motions to remand individual cases involving McKesson to California state court, and where the Court held that similar allegations against McKesson satisfied California’s permissive pleading standard for the asserted failure to warn and strict product liability claims.20 Thus, the Court finds the allegations sufficient for purposes of this motion.

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In re Zoloft (Sertraline Hydrochloride) Products Liability Litigation, 257 F. Supp. 3d 717 (E.D. Pa. 2017).

257 F. Supp. 3d 717 (In re Zoloft (Sertraline Hydrochloride) Products Liability Litigation) — published by Counsel Stack Legal Research, free access to 12M+ legal documents.

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