Pettit v. AngioDynamics, Inc.

CourtDistrict Court, D. Massachusetts
DecidedSeptember 28, 2021
Docket1:21-cv-10568
StatusUnknown

This text of Pettit v. AngioDynamics, Inc. (Pettit v. AngioDynamics, Inc.) is published on Counsel Stack Legal Research, covering District Court, D. Massachusetts primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Pettit v. AngioDynamics, Inc., (D. Mass. 2021).

Opinion

UNITED STATES DISTRICT COURT DISTRICT OF MASSACHUSETTS

* NICOLE PETTIT, * * Plaintiff, * * v. * * Civil Action No. 21-cv-10568-ADB ANGIODYNAMICS, INC. and NAVILYST * MEDICAL, INC., * * Defendants. * *

MEMORANDUM AND ORDER

BURROUGHS, D.J. In this action, which was originally filed in state court, Plaintiff Nicole Pettit brings various state law claims arising from injuries allegedly caused by a defective medical device made by Defendants AngioDynamics, Inc. (“AngioDynamics”) and Navilyst Medical, Inc. (“Navilyst,” and, together with AngioDynamics, “Defendants”). [ECF No. 1-3]. Currently before the Court are Ms. Pettit’s motion for remand, [ECF No. 12], and Defendants’ motion to dismiss for lack of personal jurisdiction, [ECF No. 8]. For the reasons set forth below, Ms. Pettit’s motion is DENIED, and Defendants’ motion is GRANTED. Ms. Pettit’s complaint, [ECF No. 1-3], is DISMISSED without prejudice. I. BACKGROUND A. Factual Background The following facts are taken primarily from the complaint, [ECF No. 1-3], the factual allegations of which are assumed to be true when considering a motion to dismiss, Ruivo v. Wells Fargo Bank, N.A., 766 F.3d 87, 90 (1st Cir. 2014). Ms. Pettit is a West Virginia resident. [ECF No. 1-3 at 3].1 AngioDynamics, and its wholly-owned subsidiary Navilyst, are Delaware corporations.2 [Id. at 4; ECF No. 1-4 ¶ 6]. In or around 2010, the U.S. Food and Drug Administration authorized Defendants to market and sell an implantable vascular access device called the SmartPort (the “Device”). [ECF

No. 1-3 at 5–6]. The Device is designed to deliver medication, intravenous fluids, parenteral nutrition solutions, and blood products directly into the bloodstream. [Id. at 6]. The Device consists of two components: an injection port and a silicone catheter. [Id.]. Due to an alleged design defect, the catheter sometimes separates from the injection port while implanted in a patient. [Id. at 7]. If such separation occurs, and the Device is being used to administer chemotherapy drugs, there can be serious medical consequences. [Id.]. Years before Ms. Pettit was implanted with the Device, Defendants received numerous adverse event reports indicating that the Device was failing because of catheter separation and causing severe injuries. [Id. at 8–9]. On October 19, 2018, Ms. Pettit was implanted with the Device at a hospital in West

Virginia. [ECF No. 1-3 at 10]. On February 13, 2019, at a routine chemotherapy session at a hospital in West Virginia, Ms. Pettit’s nurses initiated a saline flush before administering her a chemotherapy drug. [Id. at 11]. During the flush, the saline began leaking from Ms. Pettit’s chest. [Id.]. After an x-ray revealed that the Device’s catheter had become disconnected from the port, Ms. Pettit’s doctor recommended that the Device be removed. [Id.]. A few days later, the Device was surgically removed at a hospital in West Virginia. [Id.]. The surgeon who

1 Although it would typically cite to the complaint using paragraph numbers, because Ms. Pettit appears to have used certain paragraph numbers twice, the Court cites to page numbers. 2 As discussed infra, the parties dispute whether Defendants’ principal places of business are in New York or Massachusetts. removed the Device observed that the catheter was completely disconnected from the injection port. [Id.]. Because of these events, Ms. Pettit experienced significant mental and physical pain and suffering, sustained physical injuries and permanent physical deformities, underwent (and will

undergo additional) corrective surgery, and suffered financial and economic losses (including medical expenses and lost wages). [ECF No. 1-3 at 12]. B. Procedural Background Ms. Pettit filed this suit in Middlesex Superior Court on February 12, 2021. [ECF No. 1-3]. On April 5, 2021, Defendants removed the case to this Court, asserting diversity jurisdiction. [ECF No. 1]. On April 12, 2021, Defendants moved to dismiss based on lack of personal jurisdiction. [ECF No. 8]. Ms. Pettit opposed on April 30, 2021, [ECF No. 11], and Defendants replied on June 1, 2021, [ECF No. 17]. Additionally, Ms. Pettit filed a motion for remand on May 5, 2021, [ECF No. 12], which Defendants opposed on May 19, 2021, [ECF No. 16]. On July 22, 2021, Defendants filed a notice of supplemental authority. [ECF No. 20

(notice); ECF No. 20-1 (supplemental authority)]. II. MS. PETTIT’S MOTION FOR REMAND Defendants removed this case based on diversity jurisdiction. See [ECF No. 1 at 2–5]. “Federal diversity jurisdiction is available in cases arising between citizens of different states in which the amount in controversy exceeds $75,000.” Rizzi v. 178 Lowell St. Operating Co., 180 F. Supp. 3d 66, 67 (D. Mass. 2016) (citing 28 U.S.C. § 1332(a)). “Diversity jurisdiction ‘requires complete diversity between the plaintiffs and the defendants in an action.’” Id. (quoting Picciotto v. Cont’l Cas. Co., 512 F.3d 9, 17 (1st Cir. 2008)). Ms. Pettit does not contest that the complete diversity and amount in controversy requirements are met here. Instead, she argues that because Defendants are Massachusetts citizens, removal is precluded under the “forum defendant rule.” [ECF No. 13 at 2–7]. Defendants maintain that because they are not Massachusetts citizens, the “forum defendant rule” is inapplicable, and removal was therefore proper. [ECF No. 16 at 8–16].

Where, as here, removal is premised on diversity jurisdiction, it is improper “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). “This is known as the ‘forum defendant rule.’” DaSilva v. Germany, No. 19-cv-11184, 2021 WL 210788, at *2 (D. Mass. Jan. 21, 2021) (quoting Rizzi, 180 F. Supp. 3d at 68)). “A corporation’s citizenship, for diversity jurisdiction purposes, is both the state where it is incorporated and the state ‘where it has its principal place of business.’” Celli v. Greenwich Ins. Co., 478 F. Supp. 3d 93, 95–96 (D. Mass. 2020) (quoting 28 U.S.C. § 1332(c)(1)). Ms. Pettit concedes (and, in fact, specifically alleges) that both AngioDynamics and Navilyst are incorporated in Delaware. See [ECF No. 1-3 at 4]. She also alleges in her

complaint that AngioDynamics has its principal place of business in New York and Navilyst has its principal place of business in Massachusetts. See [id.]. Nevertheless, in her briefs, she maintains that both AngioDynamics and Navilyst have a principal place of business in Massachusetts. See [ECF No. 11 at 4]. Although the Court could treat Ms. Pettit’s allegation as to the location of AngioDynamics’ principal place of business as a binding judicial admission (and focus its analysis solely on Navilyst), see Schott Motorcycle Supply, Inc. v. Am. Honda Motor Co., 976 F.2d 58, 61 (1st Cir. 1992), it need not do so here because, for the reasons below, the Court finds that both AngioDynamics and Navilyst clearly have their principal places of business in New York. Several years ago, the Supreme Court established beyond any doubt that federal courts must employ the “nerve center” test to determine the location of a corporation’s principal place of business. The test is straightforward.

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