Exela Pharma Scis., LLC v. Rei Automation, Inc.

North Carolina Business Court·Decided April 2, 2026·No. 24-CVS-158·Published·Adam M. Conrad

Opinion

Exela Pharma Scis., LLC v. REI Automation, Inc., 2026 NCBC 30.

STATE OF NORTH CAROLINA IN THE GENERAL COURT OF JUSTICE SUPERIOR COURT DIVISION

CALDWELL COUNTY 24CVS000158-130

EXELA PHARMA SCIENCES, LLC, Plaintiff,

v. ORDER AND OPINION ON DEFENDANT’S MOTION FOR

REI AUTOMATION, INC., PARTIAL SUMMARY JUDGMENT Defendant.

1. This case arises out of a dispute over a contract for the development of an intravenous (IV) bag filling system. Plaintiff Exela Pharma Sciences, LLC claims that Defendant REI Automation, Inc. misrepresented its expertise and failed to design and deliver the system as promised. REI denies the allegations and blames Exela for the project’s failure. REI’s motion for partial summary judgment is now pending, as are two related motions to strike certain evidence and to supplement the record. (See ECF Nos. 61, 81, 105.) For the following reasons, the Court GRANTS REI’s summary-judgment motion and DENIES as moot its motions to strike and supplement.

Nelson Mullins Riley & Scarborough LLP, by G. Gray Wilson and Linda L. Helms, and Chintapalli Law Firm, PLLC, by Satish Chintapalli, for Plaintiff Exela Pharma Sciences, LLC.

Smith, Anderson, Blount, Dorsett, Mitchell & Jernigan, LLP, by Hope Garber, Christopher G. Smith, and Daniel Harrell, and Orrick, Herrington & Sutcliffe, LLP, by David P. Fuad, for Defendant REI Automation, Inc.

Conrad, Judge.

I.

BACKGROUND

2. The Court does not make findings of fact when deciding motions for summary judgment. The purpose of this background is to give context for the Court’s analysis and ruling.

3. Exela makes and sells pharmaceuticals. For some products, Exela uses a post-manufacturing process called terminal sterilization to reduce microbial contamination. This is done by putting the finished pharmaceutical product into an autoclave and using a combination of high pressure and high temperature to kill microbes. For products that cannot survive high temperatures, Exela uses an aseptic manufacturing process without terminal sterilization. In this context, an aseptic process broadly means that the pharmaceutical manufacturing process itself is designed to prevent or mitigate microbial contamination. (See 30(b)(6) Dep. P. Koneru 17:4–10, 18:9–19:19, 38:3–11, ECF Nos. 62.2, 72.1.)

4. REI describes itself as a builder of special or custom machinery. Its customers include pharmaceutical makers, as well as other businesses in fields as varied as the nuclear, automotive, and consumer products industries. (See Dep. M. Ahring 16:6–24, ECF Nos. 62.5, 72.11.)

5. In the summer of 2021, the parties began discussing a project to design and build a robotic, aseptic IV bag filler machine. At that time, Exela was seeking regulatory approval for a new product to be manufactured aseptically and delivered through IV bags. But its existing IV bag filler was not automated and would not have been suitable for this product. Ernest Shepard, who was then serving as Exela’s chief operating officer, had worked with REI in the past and recommended engaging it to create an aseptic robotic bag filler that could operate at scale. A series of meetings and communications followed in late July and early August 2021. During these preliminary discussions, Exela’s representatives toured REI’s facilities, and REI told Exela that it was in the process of building an aseptic IV bag filling system for another company. (See 30(b)(6) Dep. P. Koneru 93:6–94:20, 135:2–136:17; Dep. E. Shepard 7:17–8:9, 71:4–72:22, ECF Nos. 62.3, 72.2; Dep. M. Pope 50:3–51:14, ECF Nos. 62.4, 72.5; Aff. E. Shepard ¶¶ 2, 3, ECF No. 72.6.)

6. At the end of October 2021, REI tendered a proposal in which it touted its “core competencies” as its “ability to develop elegant, robust automation system designs from fully automatic assembly lines to robotic cells to semi-automatic lean assembly cells.” The proposal also contains a project description, various conceptual sketches, price and payment terms, a summary of deliverables, and more. Exela accepted the proposal and issued a purchase order just a few days later. Together, the proposal and the purchase order make up the parties’ contract. (Aff. E. Shepard Ex. A; 30(b)(6) Dep. P. Koneru Ex. 18; Dep. E. Shepard 110:2–7.)

7. REI began working on the project soon after but never completed it. The parties now blame each other for its failure. According to Exela, a third-party consulting firm assessed REI’s progress and determined that its work was shoddy and beyond salvaging. What this shows, Exela says, is that REI lacked the necessary expertise and bit off more than it could chew. REI’s answer to that charge is that it takes two to tango. As REI tells it, Exela derailed the project by withholding crucial input, repeatedly making design changes, and either firing or failing to retain most of the staff members responsible for coordinating with REI. Whatever the true reason may have been, it is undisputed that Exela terminated the project in 2023. (Compare, e.g., Decl. W. McKinney ¶¶ 2, 3, ECF No. 72.7; Dep. M. Ahring 20:13–16, with, e.g., 30(b)(6) Dep. P. Koneru 176:6–9, 191:16–192:4; Dep. G. Phillips 19:19–23, ECF No. 62.8.)

8. Exela then filed this action, complaining that it had paid REI more than $3 million with nothing to show for the effort. The complaint claims that REI breached the parties’ contract and seeks damages and declaratory relief, as well as rescission as an alternative remedy. The complaint also asserts claims for fraud and unfair or deceptive trade practices under N.C.G.S. § 75-1.1 based on the allegation that REI’s October 2021 “budget proposal . . . was false and fraudulent” because REI “knew that it lacked the expertise to fabricate” the bag filler system “in a timely manner and actively concealed . . . that it had never manufactured such products before.” By counterclaim, REI asserts that Exela breached the parties’ contract. (See, e.g., Compl. ¶¶ 6–8, 11, 13, 16, 21, 23, ECF No. 3; Ans. & Countercl., ECF No. 7.)

9. Discovery is now closed. REI has moved for partial summary judgment on Exela’s fraud and section 75-1.1 claims. During briefing on the summary-judgment motion, REI also filed a motion to strike certain evidence attached to Exela’s response brief, primarily on the ground that Exela had obtained the documents from a nonparty and then neglected to produce them to REI during discovery.

10. Once briefing on these motions was complete, the Court held a hearing on 10 February 2026. Afterward, REI moved to supplement the record, contending that Exela had mischaracterized certain evidence during the hearing. Briefing related to the motion to supplement ended on 9 March 2026.

11. REI’s motions are now ripe for resolution.

II.

LEGAL STANDARD

12. Summary judgment is proper when the record “show[s] that there is no genuine issue at to any material fact and that any party is entitled to a judgment as a matter of law.” N.C. R. Civ. P. 56(c). The Court must view the evidence in the light most favorable to the nonmoving party and draw all inferences in its favor. See Vizant Techs., LLC v. YRC Worldwide, Inc., 373 N.C. 549, 556 (2020); N.C. Farm Bureau Mut. Ins. Co v. Sadler, 365 N.C. 178, 182 (2011).

III.

ANALYSIS

13. REI’s motion targets Exela’s fraud claim. REI also contends that Exela’s section 75-1.1 claim is predicated on the fraud claim, so that the two claims rise or fall together.

14. Fraud has five “essential elements”: (a) a false representation or concealment of a material fact, (b) calculated to deceive, (c) made with intent to deceive, (d) that did in fact deceive, and (e) that resulted in damage to the injured party. Rowan Cnty. Bd. of Educ. v. U.S. Gypsum Co., 332 N.C. 1, 17 (1992). The plaintiff must show not only that it actually relied on the misrepresentation or omission but also that its reliance was reasonable. See Forbis v. Neal, 361 N.C. 519, 527 (2007).

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Exela Pharma Scis., LLC v. Rei Automation, Inc., (N.C. Super. Ct. 2026).

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