F. DENNIS SAYLOR, IV, District Judge.
This case is part of a multi-district litigation proceeding arising out of claims that the use of the drug Zofran (ondansetron) by pregnant women caused birth defects. Plaintiffs Thomas Brown and Maria Del Carmen Espindola Gomez originally filed suit in Oregon state court against defendants GlaxoSmithKline, LLC ("GSK") and Providence Health System-Oregon d/b/a Providence Newberg Medical Center f/k/a Providence Newberg Hospital ("Providence") alleging that Espindola Gomez's use of Zofran during pregnancy caused congenital heart defects in her child.
This case is before the Court for a second time, having been removed, transferred to this MDL proceeding, and then remanded three years ago. See Brown, et al. v. GlaxoSmithKline, LLC, et al., 16-cv-10215-FDS. Upon remand, and after two more years of litigation in Oregon state court, the claims against Providence were dismissed following a successful motion for summary judgment. That prompted GSK to remove the case to federal court for a second time. Plaintiffs have again moved to remand, contending that the removal was untimely and barred by the "voluntary-involuntary" doctrine. With plaintiffs' motion to remand pending, the Judicial Panel for Multidistrict Litigation ("MDL Panel") once again transferred the case to this district.
For the following reasons, and having considered the issue with the benefit of the state court's summary-judgment record, plaintiffs' motion to remand will be granted.
Defendant GSK distributed and sold the drug ondansetron under the brand name Zofran. Zofran was first approved in 1991 for the prevention of post-operative nausea and vomiting associated with anesthesia and for nausea and vomiting caused by radiotherapy and chemotherapy. In addition to those approved uses, GSK is alleged to have marketed Zofran "off-label" for pregnancy-related nausea and vomiting, commonly known as "morning sickness." Plaintiffs in this multidistrict litigation allege that Zofran was in fact unsafe for use in pregnant women, and that in utero exposure to Zofran caused birth defects in children born to mothers who took the drug. This particular action involves the claims of two plaintiffs: Thomas Brown and Maria Del Carmen Espindola Gomez, who are the parents of M.B. Plaintiffs sued both GSK, the manufacturer of Zofran, and Providence, a hospital located in Oregon that dispensed Zofran to Espindola Gomez.
On August 28, 2015, plaintiffs filed a complaint in Oregon state court. The complaint named GSK and Providence as defendants, and alleged seven counts arising out of congenital heart defects suffered by M.B. and allegedly caused by Espindola Gomez's use of name-brand Zofran during pregnancy. Three of those claims were brought against Providence: strict liability (Count Three); negligent misrepresentation (Count Five); and loss of consortium (Count Seven).
In October 2015, GSK removed the action to the United States District Court for the District of Oregon based on a facial challenge to the complaint, contending that Providence's citizenship should be ignored for diversity jurisdiction purposes because it was fraudulently joined. Plaintiffs moved to remand the case for lack of subject-matter jurisdiction due to a lack of complete diversity of citizenship among the parties. On January 5, 2016, the district court stayed the case pending its transfer to this district by the MDL Panel for consolidation pursuant to 28 U.S.C. § 1407.
The case was transferred by the MDL Panel to this district in February 2016. On April 21, 2016, plaintiffs renewed their motion to remand. GSK opposed remand on the ground that complete diversity existed based on the doctrine of fraudulent joinder.
The Court granted the motion to remand on June 16, 2016. It observed that under Oregon law, strict liability may attach to a "seller" of a product in a defective condition, unreasonably dangerous to the user or consumer, if the seller "is engaged in the business of selling" such a product. Or. Rev. Stat. Ann. § 30.920(1). At the time, the Oregon Supreme Court had not decided the issue of whether a healthcare provider such as a hospital may be held liable on a strict-liability claim as a "seller" of a prescription drug. However, at least two federal courts in the District of Oregon had held that such a products-liability claim against a healthcare provider may, in fact, be viable under Oregon law. Thus, and in the absence of any controlling Oregon authority, the Court concluded that there was at least a "reasonable possibility" that the Oregon Supreme Court would recognize a strict-liability claim against a healthcare provider that dispensed a pharmaceutical product. See Universal Truck & Equip. Co. v. Southworth-Milton, Inc., 765 F.3d 103, 108 (1st Cir. 2014). The Court also concluded that the allegations in the complaint, although sparse, appeared sufficient to meet the statutory requirement that Providence was in the "business of selling" Zofran as required by the statute.
The parties then litigated the case for two more years in Oregon state court. Plaintiffs' claims against Providence survived a motion to dismiss in December 2016, and the parties proceeded to discovery. At the close of discovery, Providence moved for summary judgment on the two remaining claims against it: strict liability and negligent misrepresentation.
As to the strict-liability claim, Providence contended that plaintiffs had no basis for their claims that the hospital "sold" Zofran to Espindola Gomez. It supported that contention with, among other things, the following undisputed facts:
Plaintiffs opposed the motion as to the strict-liability claim, contending that "Providence was engaged in the business of selling Zofran and that defendant sold, distributed, vended, administered and/or supplied the Zofran which caused the injuries at issue in this case." (Pls.' Resp. at 7). They supported that contention with, among other things, the following undisputed facts:
Plaintiffs voluntarily dismissed their negligent-misrepresentation claim during oral argument on October 29, 2018.
(Oct. 29, 2018 Tr. at 83-87). Following the that ruling, plaintiffs' counsel stated on the record that an appeal of the ruling "might not be needed . . . depending on the outcome of what happens with GSK." (Id. at 89).
On November 27, 2018, the Oregon trial court entered an order granting Providence's motion for summary judgment on the strict-liability claim—the only remaining claim against it—and entered a limited judgment dismissing plaintiffs' claims against Providence with prejudice. That same day, GSK removed the action to the United States District Court for the District of Oregon for a second time.
Meanwhile, on December 4, 2018, plaintiffs filed a notice of appeal with the Oregon circuit court—that is, an appeal of the limited judgment dismissing the claims against Providence. Providence then moved to dismiss the appeal on the grounds that GSK's removal of the case to federal court deprived the circuit court of jurisdiction. On February 7, 2019, the circuit court issued an order denying Providence's motion to dismiss, but holding plaintiffs' appeal in abeyance pending the federal court's disposition of the notice of removal.
Under 28 U.S.C. § 1441(a), "any civil action brought in a State court of which the district courts of the United States have original jurisdiction, may be removed by the defendant or the defendants, to the district court of the United States for the district and division embracing the place where such action is pending." By statute, this Court has subject-matter jurisdiction over, among other things, all civil actions where the amount in controversy exceeds $75,000 and where there is diversity of citizenship. See 28 U.S.C. § 1332(a). "This statutory grant requires complete diversity between the plaintiffs and defendants in an action." Picciotto v. Continental Cas. Co., 512 F.3d 9, 17 (1st Cir. 2008) (citing Strawbridge v. Curtiss, 7 U.S. (3 Cranch) 267 (1806); Halleran v. Hoffman, 966 F.2d 45, 47 (1st Cir. 1992)).
A notice of removal must be filed "within 30 days after the receipt by the defendant . . . of a copy of the initial pleading setting forth the claim for relief upon which such action or proceeding is based," 28 U.S.C. § 1446(b)(1), or "within 30 days after receipt by the defendant . . . of a copy of an amended pleading, motion, order or other paper from which it may first be ascertained that the case is one which is or has become removable." Id. § 1446(b)(3). However, "[a] case may not be removed . . . on the basis of [diversity jurisdiction] . . . more than 1 year after commencement of the action, unless the district court finds that the plaintiff has acted in bad faith in order to prevent a defendant from removing the action." Id. § 1446(c)(1). Federal courts have defined bad faith under § 1446(c)(1) as engaging in intentional conduct— action or inaction—to defeat removal. See Comer v. Schmitt, 2015 WL 5954589, at *4 (S.D. Ohio Oct. 14, 2015), rept. and recomm. adopted, 2015 WL 7076634 (S.D. Ohio Nov. 13, 2015); Ehrenreich v. Black, 994 F.Supp.2d 284, 288-89 (E.D.N.Y. 2014).
A case removed from state court must be remanded "[i]f at any time before final judgment it appears that the district court lacks subject matter jurisdiction." 28 U.S.C. § 1447(c). The removing defendant bears the burden of demonstrating the subject-matter jurisdiction of the federal court. Danca v. Private Health Care Sys., Inc., 185 F.3d 1, 4 (1st Cir. 1999). There is a presumption against removal, and any doubts as to the court's jurisdiction must be resolved in favor of remand. Tremblay v. Phillip Morris, Inc., 231 F.Supp.2d 411, 414 (D.N.H. 2002). "[A]ny legal ambiguities in the controlling state law are resolved in favor of the non-removing party and all contested factual issues and any doubt as to the propriety of the removal must be resolved in favor of remand." Nordin v. PB&J Resorts, LLC, 2016 WL 2757696, at *1 (D.N.H. May 12, 2016) (quoting Burden v. General Dynamics Corp., 60 F.3d 213, 217 (5th Cir. 1995); Renaissance Mktg., Inc. v. Monitronics Int'l, Inc., 606 F.Supp.2d 201, 208 (D.P.R. 2009)) (internal quotations omitted).
One limitation on removal is the so-called "voluntary-involuntary" doctrine, which provides that "when a case is not removable at the time it is filed, but becomes facially removable at a later date because of the dismissal of a non-diverse defendant, removal is authorized only if diversity results from a voluntary act of the plaintiff." Five Star Quality Care, Inc. v. Sunrise Senior Living, Inc., 2009 WL 1456303, at *1 (D. Mass. May 22, 2009); see also Self v. General Motors Corp., 588 F.2d 655, 658-59 (9th Cir. 1978).
"A party fraudulently joined to defeat removal . . . is disregarded in determining diversity of citizenship." Nordin, 2016 WL 2757696, at *2 (quoting Polyplastics, Inc. v. Transconex, Inc., 713 F.2d 875, 877 (1st Cir. 1983)). "In the context of fraudulent joinder, `fraudulent is a term of art' that applies to the joinder of an in-state defendant against whom plaintiff `simply has no chance of success, whatever the plaintiff's motives.'" Longden v. Philip Morris, Inc., 2003 WL 21975365, at *3 (D.N.H. Aug. 19, 2003) (quoting Hardy v. Ajax Magnathermic Corp., 122 F.Supp.2d 757, 759 (W.D. Ky. 2000)). Thus, "removal is not defeated by the joinder of a nondiverse defendant where there is no reasonable possibility that the state's highest court would find that the complaint states a cause of action upon which relief may be granted against the nondiverse defendant." Universal Truck, 765 F.3d at 108; see also Five Star Quality Care, 2009 WL 1456303, at *1 n.2 ("Fraudulent joinder occurs when a defendant against whom a plaintiff has no conceivable claim is named as a party to a lawsuit solely for the purpose of defeating federal jurisdiction.").
"Where the defendants have raised fraudulent joinder as the basis for diversity jurisdiction, that burden is a heavy one." Nordin, 2016 WL 2757696, at *1 (citing Rosbeck v. Corin Grp., PLC, 140 F.Supp.3d 197, 203 (D. Mass. 2015)). The removing party must show "that there is no reasonable possibility of a cause of action through clear and convincing evidence." Id. at *3. The analysis is "not dissimilar" to a Rule 12(b)(6) analysis. Id.; see also Longden, 2003 WL 21975365, at *3 ("[J]oinder [is] not fraudulent if [a] case can withstand a 12(b)(6) motion directed to [the] sufficiency of the cause of action.") (alteration in original) (quoting Ritchey v. Upjohn Drug Co., 139 F.3d 1313, 1319 (9th Cir. 1998)). To decide the question of fraudulent joinder, the court "may consider additional evidence beyond the claims made in the pleadings, including affidavits of the parties." See Nordin, 2016 WL 2757696, at *3 (quoting Phillips v. Medtronic, Inc., 754 F.Supp.2d 211, 215 (D. Mass. 2010)); see also Badon v. RJR Nabisco Inc., 236 F.3d 282, 284-85 & n.3 (5th Cir. 2000) (considering "undisputed summary judgment type evidence" for claim of fraudulent joinder).
Plaintiffs contend that removal was improper, and the case should be remanded, for two reasons. First, they contend that removal violated the voluntary-involuntary doctrine, because GSK filed its notice of removal after the entry of a state-court order granting a contested motion for summary judgment and entering a limited judgment eliminating the non-diverse defendant— an order that plaintiffs have appealed in the state court system. In other words, they contend that removal is barred because the dismissal of Providence was not the result of a voluntary step by plaintiffs. Second, they contend that GSK's notice of removal was untimely because it was filed more than three years after the original complaint, and outside the one-year deadline set forth in 28 U.S.C. § 1446(c)(1).
GSK counters that removal is not barred by the voluntary-involuntary doctrine because plaintiffs voluntarily dismissed their negligent-misrepresentation claim against Providence, and, in any event, the equitable exception of fraudulent joinder applies because plaintiffs fraudulently joined Providence in order to destroy complete diversity and defeat removal. In addition, GSK contends that removal was not untimely because Providence was named as a defendant in bad faith, and therefore the one-year rule does not apply.
Because the Court concludes that removal is barred by the voluntary-involuntary doctrine and the fraudulent-joinder exception does not apply, it will not reach the issue of timeliness.
Absent fraudulent joinder, GSK's removal appears to be barred by a straightforward application of the voluntary-involuntary doctrine. Diversity in this case was not created by a voluntary act of plaintiffs. Rather, GSK removed the case only after the Oregon state court granted Providence's contested motion for summary judgment on the strict-liability claim and entered a limited judgment dismissing Providence from the case. See Maine Employers, 52 F. Supp. 2d at 138. Moreover, plaintiffs subsequently filed a timely notice of appeal of that order. See id. Plaintiffs' voluntary dismissal of one claim (negligent misrepresentation) does not change the result when plaintiffs opposed the summary judgment motion as to their other claim (strict liability).
Accordingly, unless the fraudulent-joinder exception applies, removal is barred by the voluntary-involuntary doctrine.
The complaint asserts a claim for strict liability against Providence as a "seller" of the Zofran taken by Espindola Gomez. GSK contends that Providence was fraudulently joined in the action because Oregon does not recognize a cause of action against healthcare providers for strict liability. As noted, at the time of the Court's 2016 remand, the Oregon Supreme Court had not decided the issue of whether a healthcare provider such as a hospital may be held liable on a strict-liability claim as a "seller" of a prescription drug under Or. Rev. Stat. Ann. § 30.920(1). However, at least two federal courts in the District of Oregon had held that "a products liability claim against a healthcare provider . . . may, in fact, be viable under Oregon law." See Ryles v. I-Flow Corp., 2011 WL 669124, at *2 (D. Or. Feb. 17, 2011) (quoting Snyder v. Davol, Inc., 2008 WL 113902, at *1 (D. Or. Jan. 7, 2008) (citing Docken v. Ciba-Geigy, 739 P.2d 591, 594 (1987))). The parties have not provided anything to suggest that the law of Oregon has since changed.
When faced with removal of an action on the basis of alleged fraudulent joinder, courts have an "obligation to `resolv[e] . . . legal ambiguities in the controlling state law in favor of the non-removing party." Rosbeck, 140 F. Supp. 3d at 203 (quoting Bruden v. General Dynamics Corp., 60 F.3d 213, 217 (5th Cir. 1995)). Thus, in the absence of any controlling Oregon authority, the Court concludes, as it did in 2016, that at the time the complaint was filed there was at least a reasonable possibility that the Oregon Supreme Court would recognize a strictliability claim against a healthcare provider that dispensed a pharmaceutical product.
GSK further contends that even assuming a strict-liability action against Providence is viable under Oregon law, the summary judgment evidence fell short of establishing that Providence is in the "business of selling" Zofran as required by Or. Rev. Stat. Ann. § 30.920(1)(a). In other words, GSK contends that plaintiffs had no reasonable basis in fact for their claim that Providence sold Zofran to Espindola Gomez, much less that Providence was "in the business of selling" Zofran. The complaint alleged that Espindola Gomez was administered Zofran while being treated at Providence's emergency room, and that Providence sold Zofran to her while she was pregnant with M.B. (Compl. ¶¶ 27, 56). That allegation survived a motion to dismiss. Discovery then revealed at least some evidence that Providence sold her Zofran, including an invoice from Providence for the cost of the drug, and a document plaintiff signed agreeing that she was buying products from Providence.
Under the circumstances—and even though the Oregon judge ultimately concluded that plaintiffs were incorrect in their interpretation of the statute based on contrary evidence—the Court cannot say that plaintiffs had no reasonable basis in fact for their claim that Providence was in the business of selling Zofran, or that there was no reasonable possibility that an Oregon court would render that conclusion.
Finally, GSK argues that plaintiffs made "little effort to prosecute their claims against [Providence]." It specifically points to plaintiffs' failure to depose a single corporate witness;
Plaintiffs' litigation efforts against Providence certainly do not inspire confidence that they intended to prosecute their claims vigorously, and there is ample reason to suspect that the hospital was joined simply in order to defeat diversity jurisdiction. Nonetheless, under the applicable legal framework, the evidence is not sufficient to find that joinder was fraudulent and that therefore the non-diverse defendant may be disregarded. Cf. In re Avandia Mktg., Sales Practices & Prod. Liab. Litig., 2014 WL 2011597, at *3 (E.D. Pa. May 15, 2014) (finding that the plaintiffs "lack[ed] [a] genuine intent to proceed with claims against [the non-diverse defendant]" and therefore disregarding the non-diverse defendant for purposes of determining whether the court had jurisdiction).
Accordingly, the fraudulent-joinder exception does not apply, and removal is barred by the voluntary-involuntary doctrine.
In the alternative, GSK contends that even if federal jurisdiction did not properly exist when it removed the case, the Oregon district court's dismissal of Providence cured any jurisdictional issue, and a federal court therefore has jurisdiction to try the case and enter a valid judgment. See Caterpillar Inc. v. Lewis, 519 U.S. 61, 73 (1996). Had the Oregon district court not dismissed Providence, GSK further contends, the court could have severed the claims against Providence under Fed. R. Civ. P. 21, because plaintiffs can achieve complete relief in its absence, as evidenced by its counsel's statement that an appeal of the Oregon state court's summary judgment ruling "might not be needed . . . depending on the outcome of what happens with GSK." (Oct. 29, 2018 Tr. at 89). GSK characterizes that statement as an admission of plaintiffs' intent to proceed only against GSK, and contends that Providence is therefore a dispensable party, the claims against which can be severed under Rule 21.
Rule 21 provides that "[m]isjoinder of parties is not a ground for dismissing an action. On motion or on its own, the court may at any time, on just terms, add or drop a party. The court may also sever any claim against a party." Fed. R. Civ. P. 21. "In addition, `[a] court may declare a misjoinder of parties because no relief is demanded from one or more of the parties joined as defendants.'" See Varsity Wireless Inv'rs, LLC v. Town of Hamilton, 370 F.Supp.3d 292, 297 (D. Mass. 2019) (quoting 7 Fed. Prac. & Proc. Civ. § 1683). "[I]t is well settled that Rule 21 invests district courts with authority to allow a dispensable nondiverse party to be dropped at any time." Newman-Green, Inc. v. Alfonzo-Larrain, 490 U.S. 826, 832 (1989). "The decision to dismiss a non-diverse party is within discretion of the court, but this authority should be exercised `sparingly.'" Quincy Mut. Fire Ins. Co. v. Vivint Solar Developer, LLC, 2018 WL 3974820, at *4 (D. Mass. Aug. 20, 2018) (quoting Casas Office Machs., Inc. v. Mita Copystar Am., Inc., 42 F.3d 668, 677 (1st Cir. 1994)). "The decision to dismiss `revolves largely around whether the non-diverse litigant is a dispensable or indispensable party.'" Carden v. Klucznik, 775 F.Supp.2d 247, 251 (D. Mass. 2011) (quoting American Fiber & Finishing Inc. v. Tyco Healthcare Grp., LP, 362 F.3d 136, 142 (1st Cir. 2004)). At least one court in this district has held that it is improper for a Court to apply Rule 21 to drop a party where "the lack of complete diversity was apparent at the time of removal and where defendants have failed to show fraudulent joinder." See Quincy, 2018 WL 3974820, at *4 .
Under the circumstances, applying Rule 21 would "allow[] [GSK] to succeed in retaining federal jurisdiction over the case despite not being able to meet the heavy burden of proving fraudulent joinder." See id. at *5. Accordingly, the Court declines to exercise its discretion to sever the claims against Providence.
For the foregoing reasons, plaintiffs' motion to remand is GRANTED.
Plaintiffs respond that they "propounded requests for production to Providence in order to obtain documents related to Providence's communications with and purchases from GSK, documentation and billing records from the hospital which showed that Providence in turn sold Zofran to the Plaintiff, charged the Plaintiff for it, and that it was paid for, and any records which would tend to show that Providence had prior knowledge of the potential of Zofran to harm fetal development." (Pls.' Reply at 5). They further contend that "[the] depositions and the records established the prima facie elements necessary to prove that Providence sold the subject drug to the Plaintiff, that it was provided to her without alteration, and that it was administered to her in the facility. That is, the discovery was properly aimed to prove the elements of strict product liability against Providence. Put another way, no further discovery was undertaken because none was necessary." (Id.).