STEWART v. ETHICON, INC.

CourtDistrict Court, E.D. Pennsylvania
DecidedMarch 19, 2020
Docket2:19-cv-04776
StatusUnknown

This text of STEWART v. ETHICON, INC. (STEWART v. ETHICON, 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
STEWART v. ETHICON, INC., (E.D. Pa. 2020).

Opinion

IN THE UNITED STATES DISTRICT COURT FOR THE EASTERN DISTRICT OF PENNSYLVANIA

CHERYL STEWART, : : CIVIL ACTION Plaintiff, : No. 19-4776 : v. : : ETHICON, INC., and JOHNSON & : JOHNSON, : : Defendants. :

McHUGH, J. March 19, 2020 MEMORANDUM I. Introduction This case is one of several cases in this district arising out of injuries caused by alleged defects in so-called pelvic mesh devices manufactured by Ethicon, Inc., and Johnson & Johnson. In August 2019, Plaintiff Cheryl Stewart, a citizen of Texas, sued Ethicon and Johnson & Johnson in the Court of Common Pleas of Philadelphia County, pleading various state law claims for injuries allegedly caused by defects in the manufacturers’ device. The suit was filed in the Court of Common Pleas’ mass-tort program under the caption In re: Pelvic Mesh Litigation. In addition to Ethicon and Johnson & Johnson, Plaintiff also sued Secant Medical, Inc., and Secant Medical, LLC (collectively referred to as “Secant”), which produce the mesh used in the devices. Ethicon and Johnson & Johnson are citizens of New Jersey. Secant, with its principal place of business in Bucks County, is a citizen of Pennsylvania. After Plaintiff filed her state court complaint, Secant moved to dismiss. To support its motion, Secant pointed to a previous order in the same case holding that Secant was a “biomaterials supplier” and, as such, statutorily immunized under the Biomaterials Access Assurance Act (BAAA), a federal law that generally protects “biomaterial suppliers” from

liability in claims alleging injury from medical implant devices. See 21 U.S.C. § 1601 et seq. The Court of Common Pleas granted Secant’s motion to dismiss and ordered Plaintiff to file an amended complaint “that does not name any Secant entity as a defendant.” ECF 1-1, at 82 (PDF p. 98). Plaintiff complied, see ECF 1-1, at 84-85, after which Ethicon and Johnson & Johnson (hereinafter referred to as the “Removing Defendants”) removed the case to this Court, claiming diversity as the basis for the Court’s subject matter jurisdiction. ECF 1, ¶ 1. The current dispute centers on whether removal was proper. To support their claim that this Court may exercise subject matter jurisdiction, the Removing Defendants contend that complete diversity exists even though Plaintiff also named Secant, a nondiverse party, in its complaint. According to the Removing Defendants, complete diversity exists because the

nondiverse defendant was joined only to destroy diversity jurisdiction, thus implicating the “fraudulent joinder” exception to the complete diversity requirement. Id. Plaintiff responds that the nondiverse defendant was properly joined and moves to remand the case to state court. ECF 6, at 10-13. For the reasons that follow, I will deny Plaintiff’s motion to remand, and grant Removing Defendants’ motion to transfer this action to the Northern District of Texas. II. Background Resolution of the present motion to remand requires some insight into the history of litigation over these devices in the Philadelphia County Court of Common Pleas and the federal courts, as follows.1

1 For a thorough discussion of the history of this and related litigations, see Judge Kearney’s opinion in Monroe v. Ethicon, Inc., et al., No. 19-5384, at 3-9 (E.D. Pa. Dec. 23, 2019), ECF 21. 1. Suits filed in Philadelphia state court, removal to federal court, transfer to a multidistrict litigation, and remand to state court. Pelvic mesh devices manufactured by these

Removing Defendants have been controversial for years, allegedly causing injuries to many thousands of women who thought they could rely on them. As a result of these injuries, individual plaintiffs have brought lawsuits in state and federal courts across the country. In July 2013, three plaintiffs filed claims against Ethicon and other defendants, including Secant, in the Philadelphia Court of Common Pleas. After those plaintiffs filed suit, Ethicon removed each case to this Court. See In re Ethicon, Inc. Pelvic Repair Sys. Prod. Liab. Litig., 2013 WL 6710345, at *1 (S.D.W. Va. Dec. 19, 2013). After removal, but before any additional motions practice, the cases were transferred to a multidistrict litigation (MDL) that had been established in the United States District Court for the Southern District of West Virginia. That MDL was tasked to handle various individual pelvic mesh cases filed against Ethicon and

Johnson & Johnson. See In re Ethicon, Inc., Pelvic Repair Sys. Prod. Liab. Litig., MDL No. 2327, 2019 WL 385423, at *2 (S.D.W. Va. Jan. 30, 2019) (discussing the history of the multidistrict litigation, hereinafter referred to as the Southern District of West Virginia MDL). Once transferred to the Southern District of West Virginia MDL, the plaintiffs moved to remand their cases back to the Philadelphia Court of Common Pleas. In doing so, plaintiffs argued that Ethicon’s removal of the state court actions was barred by the “forum defendant rule” because Secant, a citizen of Pennsylvania, was named as a defendant in the original complaint. The forum-defendant rule provides that an action otherwise removable based on diversity jurisdiction “may not be removed if any of the parties in interest properly joined and

served as defendants is a citizen of the State in which such action is brought.” 28 U.S.C. § 1441(b)(2). In its opposition to plaintiffs’ motion to remand, Ethicon argued that Secant was “fraudulently joined” because it was immune from liability as a “biomaterials supplier” under the

BAAA. The BAAA generally provides that “a biomaterials supplier”—an entity that supplies either raw materials or component parts for medical implants—“shall not be liable for harm to a claimant caused by an implant.” 21 U.S.C. § 1604(a). To effectuate that goal, for parties believing themselves to be biomaterials suppliers, the BAAA created an “expeditious” motion to dismiss procedure. See 21 U.S.C. §§ 1601(15)(B), 1605(a). Suppliers such as Secant can secure dismissal by establishing: (1) that it is “a biomaterials supplier”; (2) that it is not liable as a “manufacturer” or “seller” of the failed implant as those terms are narrowly defined by the Act; and (3) that it did not furnish raw materials or component parts for an implant that failed to meet applicable contractual requirements or specifications. 21 U.S.C. § 1604(a), (b), (d). The plaintiffs disputed that the BAAA immunized Secant but maintained that whether

Secant ultimately was protected by the BAAA was legally irrelevant. They noted that the fraudulent joinder doctrine placed a “heavy burden” on the party seeking to invoke it to show that “there is no possibility that the plaintiff would be able to establish a cause of action against the in-state defendant in state court.” In re Ethicon, Inc. Pelvic Repair Sys. Prod. Liab. Litig., 2013 WL 6710345, at *2 (quoting Hartley v. CSX Transp., Inc., 187 F.3d 422, 424 (4th Cir. 1999)). Plaintiffs argued that they had presented enough evidence that the BAAA may be applicable to Secant, which they believed was sufficient to defeat a claim of fraudulent joinder. In December 2013, the Southern District of West Virginia MDL granted plaintiffs’ motion to remand. Id. at *1. In doing so, the court reasoned that “the dearth of case law

interpreting the B.A.A.A.” made it “difficult to determine whether the B.A.A.A. is applicable to Secant.” Id. at *3.

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