Block Scientific, Inc. v. True Diagnostics, Inc.

District Court, S.D. California·Decided January 3, 2023·No. 3:21-cv-01118·Unknown

Opinion

BLOCK SCIENTIFIC, INC., Case No.: 3:21-cv-01118-RBM-JLB

Plaintiff, ORDER GRANTING IN PART AND v. DENYING IN PART MOTION TO DISMISS FIRST AMENDED COMPLAINT SYNTRON BIORESEARCH, INC., et al., Defendants. [Doc. 22] On April 1, 2022, Syntron Bioresearch, Inc. (“Syntron”) and True Diagnostics, Inc. (“True Diagnostics”) (collectively the “Suppliers” or “Defendants”) filed a motion to dismiss portions of the first amended complaint (“FAC”) filed by Plaintiff Block Scientific, Inc. (“Plaintiff”). (Doc. 22 (“MTD”).) Plaintiff filed its opposition to the MTD on April 28, 2022. (Doc. 25 (“Opp.”).) Defendants filed a response in support of their MTD on May 5, 2022. (Doc. 28 (“Reply”).) The Court took the matter under submission without oral argument pursuant to Civil Local Rule 7.1(d)(1). (Doc. 24.) For the reasons discussed below, the MTD is GRANTED IN PART AND DENIED Syntron and True Diagnostics are “the purported suppliers of an alleged COVID-19 antibody testing kit known as the ‘QuikPac II IgG & IgM COVID-19 Test Kit’ (the ‘QuikPac Test’), through their respective agents, Jerry Lee and Arjang Amini.” (Doc. 19, First Amended Complaint (“FAC”) ¶ 2.) Plaintiff asserts that in March 2020, Plaintiff learned that the Suppliers “had purportedly developed a serology test to identify IgG and IgM antibodies to SARS-CoV-2 in human serum, plasma, or whole blood, called the QuikPac Test.” (Id. ¶ 31.) Plaintiff and the Suppliers had numerous conversations about the QuikPac Test in March and April 2020, “including with respect to its legality, availability, and sensitivity and specificity testing results.” (Id. ¶ 32.) Plaintiff claims the Suppliers represented during these conversations that they would abide by all requirements set by the United States Food and Drug Administration (“FDA”) for serology testing, including obtaining all applicable authorizations and approvals. (Id. ¶¶ 32–33.) Additionally, Plaintiff alleges the Suppliers represented “the QuikPac Test was highly effective and would exceed the minimum sensitivity and specificity required by the FDA,” including in product inserts provided to Plaintiff in which the Suppliers “represented that the QuikPac Test scored IgG PPA sensitivity and specificity rates well in excess of 90%.” (Id. ¶ 33.) On April 15, 2020, Plaintiff and the Suppliers executed a Manufacturing Supply Agreement (the “Agreement”)1 for the manufacture and sale of QuikPac Tests, which Plaintiff planned to distribute to its customers in the United States. (Id. ¶ 34.) “In accordance with the Agreement and its customers’ purchase orders, Block Scientific tendered $2,028,695.00 to Syntron.” (Id. ¶ 35.) Plaintiff alleges it was fraudulently induced to enter the Agreement due to two of the Suppliers’ allegedly misleading or fraudulent statements: “(1) that the QuikPac Test was manufactured by Syntron in its Carlsbad, California facility; and (2) that Syntron submitted a Premarket Notification to the FDA and that the FDA’s device listing website would show Syntron as the 1 The Manufacturing Supply Agreement is attached to Plaintiff’s FAC as Exhibit A. (See manufacturer of the QuikPac Test.” (Id. ¶ 36.) Plaintiff alleges that, in reliance on the parties’ Agreement and the Suppliers’ fraudulent assurances, Plaintiff entered contracts with two of its own customers, Meridian Bioscience, Inc. (“Meridian”) and Hopco for the sale of QuikPac Tests. (Id. ¶ 54.) Plaintiff’s agreements with Meridian and Hopco were collectively worth millions of dollars in sales to Plaintiff, and included the potential for tens of millions of dollars more in future sales. (Id. ¶ 57.) Plaintiff alleges the Suppliers “were well aware of the existence and significance of” Plaintiff’s contracts with Meridian and Hopco because Plaintiff and the Suppliers “had multiple telephonic and written communications with Hopco and Meridian, beginning in April 2020, regarding the parties’ respective commitments and expectations.” (Id. ¶ 58.) Plaintiff alleges the Suppliers’ conduct disrupted its contracts with Meridian and Hopco. First, “Defendants continuously failed to deliver the QuikPac Tests on time, altered production timelines and missed production schedules, and failed to properly communicate delays.” (Id. ¶ 62.) Additionally, “in June 2020, Block Scientific learned that Defendants failed to properly submit a Premarket Notification to the FDA for the QuikPac Tests by failing to list Syntron as the manufacturer of the QuikPac Tests on the FDA’s website.” (Id. ¶ 64.) Plaintiff alleges that, upon learning the Suppliers failed to properly submit the Premarket Notification, both Hopco and Meridian cancelled their contracts with Plaintiff and requested refunds, which Plaintiff timely issued. (Id. ¶¶ 65–69.) The Suppliers also informed Plaintiff in July 2020 “that the QuikPac Test failed a serology test evaluation, scoring an IgG PPA/sensitivity rate of only 73.3%, far below the minimum sensitivity and specificity required by the FDA.” (Id. ¶ 67.) At this point, the QuikPac Tests were immediately withdrawn from the market. (Id.) On June 15, 2021, Plaintiff filed suit for breach of contract, intentional interference with contractual relations, intentional interference with prospective economic relations, and negligent interference with prospective economic relations against Syntron and True Diagnostics. (See generally Doc. 1.) On August 17, 2021, Syntron and True Diagnostics filed a motion to dismiss the complaint pursuant to Federal Rule of Civil Procedure 12(b)(6). (Doc. 7.) The Honorable Janis L. Sammartino granted in part and denied in part the motion on February 16, 2022. (See Doc. 15.) Specifically, Judge Sammartino dismissed without prejudice Plaintiff’s claims for intentional interference with contractual relations, intentional interference with prospective economic relations claims, and negligent interference with prospective economic relations. (Id.) Judge Sammartino also dismissed Plaintiff’s breach of contract claim without prejudice to the extent that claim was based on Syntron’s and True Diagnostics’ purported failure to timely deliver the QuikPac Tests or properly submit the QuikPac Test for emergency use authorization to the FDA, but denied the motion to dismiss the breach of contract claim as to Plaintiff’s allegations that the QuikPac Test was less effective than Syntron and True Diagnostics represented, which led to the Suppliers’ failure to obtain Emergency Use Authorization for the QuikPac Test. (See id. at 6–12, 19–20.) Plaintiff was granted leave to file an amended complaint within 30 days of the Court’s order, which it did on March 18, 2022. (Doc. 19.) Plaintiff added two defendants in its FAC: Jerry Lee (“Lee”), the founder and Chief Executive Officer of True Diagnostics, and Arjang Amini (“Amini”), the Quality Assurance Manager of Syntron. (FAC ¶¶ 19–20.) The FAC alleges four causes of action: (1) breach of contract against True Diagnostics and Syntron; (2) money had and received against True Diagnostics and Syntron; (3) fraudulent inducement against all defendants; and (4) rescission against True Diagnostics and Syntron. (Id. ¶¶ 76–105.) The Suppliers filed the instant MTD on April 1, 2022, seeking dismissal of Plaintiff’s claims for breach of contract, money had and received, and rescission. (MTD at 2.)2 This action was transferred to the undersigned on April 7, 2022. (Doc. 23.) Under Federal Rule of Civil Procedure (“Rule”) 12(b)(6), a party may move to 2 True Diagnostics and Syntron do not seek dismissal of Plaintiff’s third claim for dismiss a complaint for “failure to state a claim upon which relief can be granted.” FED. R. CIV. P. 12(b)(6). At the motion to dismiss stage, all material factual allegations in the complaint are accepted as true and are construed in the

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Block Scientific, Inc. v. True Diagnostics, Inc., (S.D. Cal. 2023).

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