Gelt Trading v. Co-Diagnostics

District Court, D. Utah·Decided August 18, 2023·No. 2:20-cv-00368·Unknown

Opinion

IN THE UNITED STATES DISTRICT COURT FOR THE DISTRICT OF UTAH

GELT TRADING LTD., MEMORANDUM DECISION AND ORDER PARTIALLY GRANTING Plaintiff, MOTION FOR CLASS v. CERTIFICATION, APPOINTMENT OF CLASS REPRESENTATIVE, AND CO-DIAGNOSTICS, INC.; DWIGHT APPOINTMENT OF CLASS COUNSEL EGAN; JAMES NELSON; EUGENE DURENARD; EDWARD MURPHY; Case No. 2:20-CV-00368-JNP-DBP RICHARD SERBIN; REED BENSON; and BRENT SATTERFIELD, District Judge Jill N. Parrish

Defendants. Magistrate Judge Dustin B. Pead

Pursuant to Federal Rule of Civil Procedure 23, lead plaintiff Gelt Trading Ltd. (“Gelt”) moves for the court to order (i) the certification of a class of investors in Co-Diagnostics, Inc. (“Co-Diagnostics”) defined as all those who purchased the securities of Co-Diagnostics between May 1, 2020 and May 15, 2020 inclusive, and who were damaged thereby, (ii) the appointment of Gelt as class representative, and (iii) the appointment of Armstrong Teasdale, LLP, Marcus Neiman Rashbaum & Pineiro LLP, and Fasano Law Firm, PLLC, as co-class counsel. ECF No. 114. Co-Diagnostics and several of the company’s executives (“Defendants”) oppose this motion by arguing that Gelt has failed to establish commonality, typicality, and adequacy, as required by Rule 23(a). Having reviewed the parties’ memoranda, the court PARTIALLY GRANTS Gelt’s motions. FACTUAL BACKGROUND Co-Diagnostics is a Utah Corporation that develops and sells diagnostic tests for several diseases, including zika virus, tuberculosis, hepatitis B and C, malaria, dengue fever, and HIV. When the COVID-19 pandemic began in early 2020, the corporation developed a test to detect the disease. On February 24, 2020, Co-Diagnostics announced that it was the first company to receive regulatory approval to sell its COVID-19 tests in the European Economic Area. Its stock price rose sharply on this news. On April 6, 2020, the U.S. Food and Drug Administration (“FDA”) likewise

granted Co-Diagnostics’ COVID-19 test emergency use authorization. Co-Diagnostics’ new test led to lucrative contracts at home and abroad. It sold tests to fifty countries and more than twelve U.S. states. Co-Diagnostics also agreed to provide the majority of the COVID-19 tests for a $5 million contract between TestUtah and the state of Utah. It entered a similar agreement related to a $26 million contract in Iowa. Co-Diagnostics’ value grew accordingly. The company has been publicly listed on the NASDAQ since July 12, 2017. Prior to the pandemic, Co-Diagnostics stock regularly traded for under a dollar. As its COVID-19 test found success, the company’s stock price reached an all-time high of $29.72 per share. But medical experts began raising concerns about Co-Diagnostics’ COVID-19 tests. On

April 30, 2020, the Salt Lake Tribune published an article questioning the accuracy of its tests. Specifically, the Tribune reported that the TestUtah sites that used Co-Diagnostics’ tests saw a 2% positivity rate, whereas other sites across the state saw a positivity rate closer to 5%. One doctor called this discrepancy “a potential public health disaster.” ECF No. 91-2. In the article, the Tribune quoted Brent Satterfield, Co-Diagnostics’ Chief Science Officer, as stating that studies had shown that the tests were between 99.52% and 100% accurate. On May 1, 2020, Co- Diagnostics issued a press release claiming that multiple independent evaluations had shown that its tests were 100% accurate. On May 14, 2020, Co-Diagnostics stock reached its highest ever price. But that day journalists again began questioning the company’s claims of 100% test accuracy. The Salt Lake Tribune reported that the state of Utah had declined to join other major Utah labs in a joint experiment to confirm one another’s testing quality. The Tribune article also stated that Co-

Diagnostics tests required a higher concentration of the COVID-19 virus than other tests to register a positive result. Soon thereafter, the Governor of Iowa issued a public statement explaining that the test was 95% accurate in determining positive results and 99.7% accurate in determining negative results. Later that day, the FDA issued a press release stating that no test would be 100% accurate. Co-Diagnostics’ stock price declined as this news broke. On May 14, the stock’s trading was stopped twice. Ultimately, Co-Diagnostics’ stock value went from a high of $29.52, to an intra-day low of $18.35, before closing at $22.13. The next day, May 15, the stock opened at a price of $15.80 per share. Gelt, a Cayman Island limited liability company purchased Co-Diagnostics shares on May 14 prior to the release of news pertaining to the COVID-19 test’s inaccuracy. Gelt claims that, as

a result of Defendants’ allegedly misleading statements, it lost $117,845.87 when the stock price fell. On June 15, 2020, it filed a class action lawsuit against Co-Diagnostics and its officers and directors for violations of Sections 10(b) and 20(a) of the Securities Exchange Act of 1934. ECF No. 1. Gelt alleged that the injured class of investors it represented included all individuals who purchased Co-Diagnostics stock between February 25, 2020 and May 15, 2020. But Gelt never served this initial complaint. On July 15, 2020, it filed an amended complaint. The amended complaint shortened the proposed class period to those who purchased Co-Diagnostics stock from April 30, 2020 to May 15, 2020. ECF No. 14. It served this amended complaint to the relevant parties. On March 10, 2021, the court appointed Gelt lead plaintiff. ECF No. 84. Soon thereafter, Gelt filed a second amended complaint, which became the subject of a motion to dismiss filed by Defendants on May 5, 2021. ECF No. 86; ECF No. 91. The court partially denied Defendants’ motion on March 9, 2022; however, it dismissed the portion of the claim alleging a misstatement

on April 30, 2020. ECF No. 101 at 14. As a result of this ruling, the putative class could only include those who purchased shares of Co-Diagnostics between May 1, 2020, and May 15, 2020, inclusive. Id. Following the court’s decision to allow this case to move forward, on October 17, 2022, Gelt filed the present motion for class certification. ECF No. 114. LEGAL STANDARD To certify a class, a plaintiff must satisfy four requirements under Fed. R. Civ. P. 23(a): numerosity, commonality, typicality, and adequacy. A proposed class must also fit into one of the subdivisions of Fed. R. Civ. P. 23(b). Gelt seeks class certification under Rule 23(b)(3), which requires that questions of law or fact common to the class “predominate over any questions affecting only individual members” and that “a class action is superior to other available methods for fairly and efficiently adjudicating the controversy.” Fed. R. Civ. P. 23(b)(3).

Class certification is “committed to the discretion of the trial court.” Anderson v. City of Albuquerque, 690 F.2d 796, 799 (10th Cir. 1982). Plaintiffs bear the burden of establishing class certification by a preponderance of evidence. See Shook v. El Paso Cnty., 386 F.3d 963, 968 (10th Cir. 2004). Courts “must accept the substantive allegations of the complaint as true . . . although [they] need not blindly rely on conclusory allegations . . . and may consider the legal and factual issues presented by plaintiff’s complaints.” Id. (cleaned up).

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Gelt Trading v. Co-Diagnostics, (D. Utah 2023).

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