KIMBERLY ANN SCIANDRA, as Administrator of the ESTATE OF MARSHA KATHLEEN SCIANDRA v. INSULET CORPORATION; DEXCOM, INC.; US MED, LLC; and CARY ENDOCRINE & DIABETES CENTER, P.A.

CourtDistrict Court, E.D. North Carolina
DecidedDecember 2, 2025
Docket5:25-cv-00519
StatusUnknown

This text of KIMBERLY ANN SCIANDRA, as Administrator of the ESTATE OF MARSHA KATHLEEN SCIANDRA v. INSULET CORPORATION; DEXCOM, INC.; US MED, LLC; and CARY ENDOCRINE & DIABETES CENTER, P.A. (KIMBERLY ANN SCIANDRA, as Administrator of the ESTATE OF MARSHA KATHLEEN SCIANDRA v. INSULET CORPORATION; DEXCOM, INC.; US MED, LLC; and CARY ENDOCRINE & DIABETES CENTER, P.A.) is published on Counsel Stack Legal Research, covering District Court, E.D. North Carolina primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

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KIMBERLY ANN SCIANDRA, as Administrator of the ESTATE OF MARSHA KATHLEEN SCIANDRA v. INSULET CORPORATION; DEXCOM, INC.; US MED, LLC; and CARY ENDOCRINE & DIABETES CENTER, P.A., (E.D.N.C. 2025).

Opinion

IN THE UNITED STATES DISTRICT COURT FOR THE EASTERN DISTRICT OF NORTH CAROLINA WESTERN DIVISION

NO. 5:25-CV-519-FL

KIMBERLY ANN SCIANDRA, as ) Administrator of the ESTATE OF ) MARSHA KATHLEEN SCIANDRA, ) ) Plaintiff, ) ) v. ) ORDER ) INSULET CORPORATION; DEXCOM, ) INC.; US MED, LLC; and CARY ) ENDOCRINE & DIABETES CENTER, ) P.A., ) ) Defendants. )

This matter is before the court on plaintiff’s motion to remand (DE 33), which motion has been briefed fully, and is ripe for ruling. Also pending is a motion for leave to file sur-reply filed by defendants Dexcom, Inc. (“Dexcom”), Insulet Corporation (“Insulet”), and US Med, LLC (“US Med”), in which said defendants seek to address issues allegedly raised for the first time in plaintiff’s reply in support of her motion to remand. (DE 44). For the following reasons, the court grants the motion for leave to file sur-reply, and upon consideration of the briefing thus expanded the court grants the motion for remand. STATEMENT OF THE CASE Plaintiff commenced this products liability and negligence action June 27, 2025, in Wake County Superior Court, asserting claims arising out of the death of Marsha Kathleen Sciandra (“decedent”) following her use of an insulin pump and monitoring system allegedly designed, manufactured, assembled, inspected, maintained, sold, marketed, distributed, and/or supplied by defendants. Plaintiff asserts seventeen claims in the following categories: 1. “Negligent, grossly negligent, reckless, willful, and wanton conduct” of all defendants,1 2. “Breach of express and implied warranties” by all defendants, 3. “Chapter 75 violations” by defendants Insulet, Dexcom, and US Med,

4. “Negligent and wanton misrepresentation” by defendants Insulet, Dexcom, and US Med, and 5. “Punitive damages” against defendants Insulet, Dexcom, and US Med. (Compl. (DE 1-9) 8, 12, 14, 17-19, 23, 25, 28, 30, 34, 36, 39, 41, 45).2 Plaintiff seeks compensatory and punitive damages, costs and interest. Defendant Insulet filed notice of removal in this court August 22, 2025, asserting jurisdiction under 28 U.S.C. § 1332(a), on the basis of diversity jurisdiction. While acknowledging that defendant Cary Endocrine & Diabetes Center, P.A. (“Cary Endocrine”), is a North Carolina business entity, defendant Insulet asserts that “Cary Endocrine is fraudulently joined” or claims

against it should be severed to preserve diversity jurisdiction. (Notice of Removal (DE 1) at 2). Plaintiff thereafter filed the instant motion to remand, on the basis that the court lacks diversity jurisdiction, defendant Cary Endocrine was not fraudulently joined, and claims against it are not severable. Plaintiff relies upon her own declaration. Defendants3 filed a response in

1 The caption of the claim against defendant US Med is limited to “Negligent and wanton conduct,” but the substance of the claim encompasses also gross negligence, recklessness, and willfulness. (Compl. (DE 1-9) at 30-32).

2 In citations to the complaint and other filings in the record, page numbers in citations specify the page numbers supplied by the court’s case management / electronic case filing (“CM/ECF”) system and not the page numbers, if any, showing on the face of the documents.

3 Hereinafter, all references to “defendants” in the instant order are to defendants Insulet, Dexcom, and US Med, to the exclusion of defendant Cary Endocrine, unless otherwise specified. opposition, relying upon articles of incorporation of Cary Endocrine and an affidavit of Sung-Eun Yoo, M.D. (“Yoo”), owner of Cary Endocrine. Plaintiff replied, relying upon a supplemental affidavit. Defendants then filed the instant motion for leave to file sur-reply, relying upon a proposed sur-reply. STATEMENT OF THE FACTS

The facts alleged in the complaint, as pertinent to the instant motion, may be summarized as follows. Decedent “was a Type 1, insulin dependent diabetic from the age of three years old until her death at the age of seventy-five on August 27, 2023.” (Compl. ¶ 23). “The Omnipod 5 is a wearable, tubeless automated insulin delivery system designed to manage diabetes by delivering insulin subcutaneously.” (Id. ¶ 24). “The Omnipod 5 is used in conjunction with a continuous glucose monitoring system and is specifically designed to be compatible with the Dexcom G6 CGMS.” (Id.). “Used together, these devices are designed to automatically adjust insulin delivery based on a patient’s blood glucose level to more effectively manage diabetes.” (Id.). “Elevated

or depressed blood glucose levels during sleep can be particularly dangerous because diabetics are unaware of fluctuations. Dexcom designed and markets the Dexcom G6 CGMS as being able to alert and awaken users who become hypo or hyperglycemic.” (Id. ¶ 25). Decedent “was sold the Omnipod 5 insulin pump on August 4, 2022 by [defendant] Cary Endocrine.” (Id. ¶ 26). She “utilized the Dexcom G6 CGMS and the Omnipod 5 as part of her diabetes management plan.” (Id. ¶ 27). “Upon information and belief, [decedent’s] Omnipod 5 and Dexcom G6 units were sold by [defendant] US Med.” (Id. ¶ 28). “After beginning use of the Omnipod, [decedent] experienced difficulty in maintaining her blood glucose at safe levels, reporting sustained elevated blood glucose levels after meals and overnight despite receiving insulin via the pump.” (Id. ¶ 29). “On August 8, 2023, [decedent’s] blood glucose level was persistently elevated throughout the day.” (Id. ¶ 30). “That evening, after receiving [an elevated] blood glucose reading . . . on her Dexcom, she directed the Omnipod to administer several doses of insulin to bring her level down.” (Id.). “The Omnipod registered that the doses were given.” (Id.).

“Believing the insulin to be delivered, [decedent] went to bed.” (Id. ¶ 31). The next morning, decedent’s husband found decedent “collapsed on the bedroom floor,” and he called emergency medical services, which determined decedent had highly elevated blood glucose level. (Id. ¶ 32). Decedent’s blood glucose level further increased upon hospital admission. (Id.). Decedent was “diagnosed and treated for severe diabetic ketoacidosis (OKA), acute kidney injury, and hypotension.” (Id. ¶ 33). Despite aggressive treatment, her “condition deteriorated, leading to her death on August 27, 2023.” (Id.). Decedent’s “attending physician . . . discovered that the Omnipod unit used by [decedent] at the time of injury had a bent needle.” (Id. ¶ 34). “As a result, the Omnipod had not

subcutaneously delivered the insulin as designed.” (Id.). “Despite having a warning system to alert users to other sources of needle occlusion, the alert does not function when the needle is bent.” (Id.). According to the complaint defendant Cary Endocrine “derives profit from inspecting, testing, warning, advertising, promoting, and supplying [the] Omnipod [and] Dexcom” products, “including, but not limited to, the Omnipod 5 and Dexcom G6 CGMS being used” by decedent. (Id. ¶ 175). It “produced, advertised, sold, and supplied” the subject Omnipod 5 and Dexcom G6 CGMS, which was defective in manufacture” and “in design.” (Id. ¶ 176). It “failed to properly test,” “inspect,” “provide appropriate manuals,” and “provide adequate and appropriate warnings,” and it “continued to make statements touting the reliability and safety of” the Omnipod and Dexcom products. (Id. ¶ 178). Plaintiff also alleges that defendant Cary Endocrine “by and through its officers, managers, agents, suppliers, contractors, subcontractors, representatives, and others for whom they are legally responsible, in order to induce the purchase of Omnipod 5 and Dexcom G6 CMGS devices, which

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KIMBERLY ANN SCIANDRA, as Administrator of the ESTATE OF MARSHA KATHLEEN SCIANDRA v. INSULET CORPORATION; DEXCOM, INC.; US MED, LLC; and CARY ENDOCRINE & DIABETES CENTER, P.A., Counsel Stack Legal Research, https://law.counselstack.com/opinion/kimberly-ann-sciandra-as-administrator-of-the-estate-of-marsha-kathleen-nced-2025.