Harness v. AngioDynamics, Inc.

CourtDistrict Court, D. Massachusetts
DecidedSeptember 28, 2021
Docket1:21-cv-10233
StatusUnknown

This text of Harness v. AngioDynamics, Inc. (Harness 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
Harness v. AngioDynamics, Inc., (D. Mass. 2021).

Opinion

UNITED STATES DISTRICT COURT DISTRICT OF MASSACHUSETTS

* DAVID HARNESS, * * Plaintiff, * * v. * * Civil Action No. 21-cv-10233-ADB ANGIODYNAMICS, INC. and NAVILYST * MEDICAL, INC., * * Defendants. * *

MEMORANDUM AND ORDER

BURROUGHS, D.J. Plaintiff David Harness alleges that he was injured 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 Mr. Harness’ motion for remand, [ECF No. 17], and Defendants’ motion to dismiss for lack of personal jurisdiction, [ECF No. 9]. For the reasons set forth below, Mr. Harness’ motion is DENIED, and Defendants’ motion is GRANTED. Mr. Harness’ complaint 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). Mr. Harness is a Tennessee resident. [ECF No. 1-3 ¶ 2]. AngioDynamics and Navilyst are both Delaware corporations.1 [Id. ¶¶ 3–4]. In or around 2013, Defendants received clearance from the U.S. Food and Drug Administration to market and sell a vascular access device called the BioFlo (the “Device”).

[ECF No. 1-3 ¶ 15]. The Device is designed to deliver medication, intravenous fluids, parenteral nutrition solutions, and blood products directly into the bloodstream. [Id. ¶ 18]. The Device has two parts: an injection port and a polyurethane catheter. [Id. ¶ 20]. Because of an alleged design and manufacturing defect, the catheter sometimes fractures. [Id. ¶¶ 23–29]. If a catheter fractures, the results can be life-threatening. See [id. ¶ 37]. Years before Mr. Harness was implanted with the Device, Defendants received numerous adverse event reports indicating that catheters were fracturing and pieces were migrating through users’ bodies, with catastrophic consequences. [Id. ¶ 38]. On July 31, 2019, Mr. Harness was implanted with the Device at a hospital in Tennessee. [ECF No. 1-3 ¶ 47]. On January 8, 2020, the Device, and fractured fragments from its catheter,

were surgically removed from Mr. Harness also at a hospital in Tennessee. [Id. ¶ 48]. As a result of the Device fracturing, Mr. Harness 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). [Id. ¶ 56].

1 As discussed infra, the parties dispute whether Defendants’ principal places of business are in New York or Massachusetts. B. Procedural Background Mr. Harness filed this suit in Middlesex County Superior Court on December 23, 2020. [ECF No. 1-3]. On February 11, 2021, Defendants removed the case. [ECF No. 1]. On February 18, 2021, Defendants moved to dismiss based on lack of personal jurisdiction. [ECF

No. 9]. Mr. Harness opposed on March 11, 2021, [ECF No. 14], and Defendants replied on April 5, 2021, [ECF No. 21]. Additionally, Mr. Harness filed a motion for remand on March 12, 2021, [ECF No. 17], which Defendants opposed on April 9, 2021, [ECF No. 22]. On April 28, 2021, Mr. Harness filed a notice of supplemental authority, [ECF No. 25], to which Defendants responded on May 3, 2021, [ECF No. 28]. On July 22, 2021, Defendants filed a notice of supplemental authority of their own. [ECF No. 31 (notice); ECF No. 31-1 (authority)]. Finally, on September 1, 2021, Mr. Harness filed a motion to consolidate this case with four similar cases also before the Court, [ECF No. 32], which the Court will address in a separate Order. II. MR. HARNESS’ 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)). Mr. Harness concedes that the diversity and amount-in-controversy requirements are met here but maintains that because Defendants are Massachusetts citizens, removal is prohibited by the “forum defendant rule.” [ECF No. 16 at 3 (emphasis omitted)]. Defendants respond that the “forum defendant rule” is inapplicable because they are not Massachusetts citizens. [ECF No. 22 at 8–15]. 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)). Mr. Harness does not dispute (and, in fact, specifically avers) that Defendants are incorporated in Delaware. [ECF No. 1-3 ¶¶ 3–4]. In his complaint, he alleges that AngioDynamics and Navilyst have their principal places of business in New York and Massachusetts, respectively. [Id.]. Nevertheless, in his briefs, he contends that both Defendants have their principal places of business in Massachusetts. See [ECF No. 16 at 3–7]. Although the Court could treat Mr. Harness’ allegation that AngioDynamics’ principal place of business is in New York as a binding judicial admission (and focus exclusively 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 that follow, 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. A corporation’s “nerve center” (i.e., its principal place of business) is the particular location from which its “officers direct, control, and coordinate the corporation’s activities.” Generally speaking, this will “be the place where the corporation maintains its headquarters—provided that the headquarters is the actual center of direction, control, and coordination . . . and not simply an office where the corporation holds its board meetings (for example, attended by directors and officers who have traveled there for the occasion).” Harrison v. Granite Bay Care, Inc., 811 F.3d 36, 40 (1st Cir. 2016) (citations omitted) (quoting Hertz Corp. v. Friend, 559 U.S. 77, 80–81, 92–93 (2010)). “At its heart, the nerve center test is an inquiry to find the one location from which a corporation is ultimately controlled.” Id. at 41. Applying the nerve center test to the facts at hand leads to the conclusion that

Defendants’ principal places of business are in New York. According to an affidavit filed by Stephen A.

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