Kitchen v. AngioDynamics, Inc.

CourtDistrict Court, N.D. Ohio
DecidedJune 28, 2024
Docket1:24-cv-00132
StatusUnknown

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

Bluebook
Kitchen v. AngioDynamics, Inc., (N.D. Ohio 2024).

Opinion

IN THE UNITED STATES DISTRICT COURT FOR THE NORTHERN DISTRICT OF OHIO EASTERN DIVISION

PATRICIA KITCHEN, ) ) Case No. 1:24-cv-00132 Plaintiff, ) ) Judge Dan Aaron Polster v. ) ) OPINION & ORDER ANGIODYNAMICS, INC., ET AL., ) ) Defendants. )

Before the Court is AngioDynamics, Inc. and Navilyst Medical, Inc.’s (“Defendants”) partial motion to dismiss under Fed. R. Civ. P. 12(b)(6), 8(a)(2), and 9(b). This products liability case stems from Plaintiff’s use of Defendants’ SmartPort device, which purportedly caused Plaintiff to develop an infection, undergo additional surgery, and sustain physical harm, emotional distress, and financial loss. For the following reasons, the Court GRANTS IN PART and DENIES IN PART Defendants’ partial motion to dismiss. The Court DISMISSES WITH PREJUDICE Counts 1, 4, 6, and 7 of Plaintiff’s amended complaint. Background and Procedural History In October 2020, Patricia Kitchen (“Ms. Kitchen” or “Plaintiff”) had an AngioDynamics SmartPort implanted, in Cleveland, Ohio, to administer her chemotherapy medication. ECF Doc. 7, ¶ 38. Generally, a SmartPort device is surgically implanted underneath the skin and designed to deliver medications directly into a patient’s blood stream. Id. at ¶¶ 13-14. In January 2022, Plaintiff experienced symptoms of an infection. Id. at ¶ 41. Plaintiff’s medical team determined that Ms. Kitchen’s SmartPort device had caused her to develop an infection. Id. One day later, Plaintiff’s medical team removed her SmartPort device. Id. at ¶ 42. As a result, Plaintiff alleges that she “experienced significant mental and physical pain and suffering, has undergone additional surgeries, and has suffered financial or economic loss, including, but not limited to, obligations for medical services and expenses.” Id. at ¶ 50. Plaintiff’s SmartPort device “is one of several varieties of port/catheter systems that has been designed, manufactured, marketed, and sold by Defendants.” Id. at ¶ 12. The SmartPort

device consists of two primary components: an injection port and a silicone catheter, the latter of which consists of “a polymeric mixture of silicone and a barium sulfate radiopacity agent.” Id. at ¶¶ 15, 18. Plaintiff contends that manufacturing and design defects caused Plaintiff’s catheter to have “too high a concentration of barium sulfate particles for the polymer formation,” which in turn led to “an irregular catheter surface replete with fissure, pits and cracks,” and thereby, “drastically increase[ed] the risk of biofilm, infection, and sepsis.” Id. at ¶¶ 19-24. Additionally, Plaintiff alleges that Defendants did not incorporate design modifications that would have made the SmartPort safer; that Defendants “misrepresented the safety of the SmartPort system;” that Defendants “failed to warn consumers” of the device’s higher failure rate compared to similar products on the market; and that Defendants “intentionally concealed the severity of

complications caused by the SmartPort and the likelihood of these events occurring.” Id. at ¶¶ 25, 26, 33, 34. On January 23, 2024, Plaintiff filed a complaint in the Northern District of Ohio. ECF Doc. 1. The complaint contained six common law product liability claims (Counts 1 through 6) and one claim under the Ohio Consumer Sales Practices Act (“CSPA”), R.C. § 1345.01 (Count 7). Id. Specifically, Plaintiff asserted claims of: Negligence (Count 1); Strict Products Liability – Design Defect (Count 2); Strict Products Liability – Failure to Warn (Count 3); Breach of Implied Warranty (Count 4); Breach of Express Warranty (Count 5); Fraudulent Concealment (Count 6); and violations of Ohio’s CSPA (Count 7). Id. On March 25, 2024, Defendants filed a motion to dismiss. ECF Doc. 5. One month later, Plaintiff filed her first amended complaint (“amended complaint”). ECF Doc. 7. The amended complaint contains the same seven claims as her original complaint, only now, Plaintiff appears to assert Counts 1 through 5 under the OPLA instead of common law. Id. Counts 2 and

3 reference a specific section of the OPLA, while Counts 1, 4, and 5 reference the entire OPLA statute. Id. Plaintiff brings the following claims in her amended complaint: Negligence, in violation of R.C. §§ 2307.71, et seq. (Count 1); Strict Products Liability – Design Defect, in violation of R.C. § 2307.75 (Count 2); Strict Products Liability – Failure to Warn, in violation of R.C. § 2307.76 (Count 3); Breach of Implied Warranty, in violation of R.C. §§ 2307.71, et seq. (Count 4); Breach of Express Warranty, in violation of R.C. §§ 2307.71, et seq. (Count 5); Fraudulent Concealment (Count 6); and violations of Ohio’s CSPA (Count 7). Id. On May 8, 2024, Defendants filed a partial motion to dismiss Counts 1, 4, 5, 6, and 7 of the amended complaint. ECF Doc. 11. On June 7, 2024, Plaintiff filed her response in opposition. ECF Doc. 16. Two weeks later, Defendants filed their reply. ECF Doc. 21.

Standard The Court may dismiss a claim when a party fails to plead facts on which relief can be granted. See Fed. R. Civ. P. 12(b)(6). “To survive a motion to dismiss, a complaint must contain sufficient factual matter, accepted as true, to ‘state a claim to relief that is plausible on its face.’ ” Ashcroft v. Iqbal, 556 U.S. 662, 678 (2009) (quoting Bell Atl. Corp. v. Twombly, 550 U.S. 544, 570 (2007)). “A claim has facial plausibility when the plaintiff pleads factual content that allows the court to draw the reasonable inference that the defendant is liable for the misconduct alleged.” Id. (citation omitted). A pleading must contain “a short and plain statement of the claim showing that the pleader is entitled to relief.” Fed. R. Civ. P. 8(a)(2). The plaintiff is not required to include “detailed factual allegations,” but must provide more than “an unadorned, the-defendant-unlawfully-harmed-me accusation.” Iqbal, 556 U.S. at 678 (citation omitted). In reviewing a complaint, this Court “must construe the complaint in the light most favorable to the plaintiff and accept all allegations as true.” Doe v. Miami Univ., 882 F.3d 579,

588 (6th Cir. 2018) (citation omitted). As the moving party, Defendants bears the burden of proof. Total Benefits Planning Agency, Inc. v. Anthem Blue Cross & Blue Shield, 552 F.3d 430, 434 (6th Cir. 2008). OPLA Analysis Defendants argue that Count 1 (Negligence), Count 4 (Breach of Implied Warranty), and Count 5 (Breach of Express Warranty) are barred because they are common law claims, and the OPLA abrogates all common law product liability claims pled outside of it. ECF Doc. 11-1, PageID# 102. Plaintiff maintains that she “has adequately pled claims pursuant to the Ohio Products Liability Act,” and the “sole basis” for Defendants’ motion is the fact that the claims “also reference the common law analogues to the statutory provisions of the OPLA.” ECF Doc.

16, PageID# 169. The essential question here is whether the allegations in Counts 1, 4, and 5 of Plaintiff’s amended complaint fall within one of the four types of claims permitted by the OPLA. Lorenzo v. Bristol-Myers Squibb Co., 2012 U.S. Dist. LEXIS 105518, at *7 (N.D.

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Kitchen v. AngioDynamics, Inc., Counsel Stack Legal Research, https://law.counselstack.com/opinion/kitchen-v-angiodynamics-inc-ohnd-2024.