Elevation Health LLC v. Americare, Inc.

District Court, D. Nevada·Decided September 29, 2024·No. 2:22-cv-01590·Unknown

Opinion

ELEVATION HEALTH, LLC, Plaintiff, Case No.: 2:22-cv-01590-GMN-NJK vs. ORDER GRANTING IN PART AND DENYING IN PART MOTION FOR AMERICARE, INC., et. al., SUMMARY JUDGMENT

Defendants. Pending before the Court is the Motion for Summary Judgment, (ECF No. 62), filed by Plaintiff and Counter Defendant Elevation Health, LLC (“Elevation”). Defendants Jennifer and Mario Gonzalez filed a Response, (ECF No. 65), to which Plaintiff filed a Reply, (ECF No. 67). For the reasons discussed below, the Court DENIES Plaintiff’s Motion as to its claims against both Jennifer and Mario Gonzalez and GRANTS Plaintiff’s Motion for Summary Judgment as to the Americare’s counterclaims. This case arises out of Elevation’s order for over-the-counter COVID-19 tests from Americare, a healthcare industry “middle-man” that sources products from suppliers and delivers them to healthcare providers. (Gonzalez Decl. ¶ 2, Ex. 1 to Resp., ECF No. 65-1). Joe Goldsmith, CEO of Plaintiff Elevation, approached Defendant Mario Gonzalez, CEO of Defendant Americare, about a need for COVID-19 antigen tests for resale over-the-counter distribution to its United States’ customers. (Id. ¶ 3). Prior to this request, Elevation had entered into at least two other contracts with Americare to purchase COVID-19 tests authorized for sale in the United States. (Goldsmith Decl. ¶ 5, Ex. 1 to Mot. Summ. J., ECF No. 62-1). To source the requested tests, Gonzalez contacted Global Health Supply and Silver Peaks Holdings, (collectively, “GHS”). (Gonzalez Decl. ¶ 4, Ex. 1 to Resp.). GHS informed him that they had Flowflex COVID-19 tests available that were approved for use by the United States Food and Drug Administration, (“FDA”). (Id.). On October 20, 2021, Mr. Kasbee, a GHS representative, sent Gonzalez an email containing several documents about the “OTC” Flowflex COVID-19 Rapid Antigen Home Test, including a FDA letter stating that the tests had been approved for emergency use authorization, (“EUA”). (Id.); (Kasbee Email, Ex. 2 to Resp., ECF No. 65-2). The email subject line is “Flowflex EUA-ACONlab-FlowflexAG-letter, Shipping Data and Specs.” (Kasbee Email, Ex. 2 to Resp.). Within an hour, Gonazlez forwarded the email to Goldsmith at Elevation without any additional text or changes to the original email from Kasbeee. (Gonzalez Decl. ¶ 5, Ex. 1 to Resp.); (Gonzalez Email, Ex. 7 to Mot. Summ. J., ECF No. 62-7). The next day, October 21, Goldsmith asked Gonzalez if he could secure the Flowflex tests for $8 per test. (Gonzalez Decl. ¶ 6, Ex. 1 to Resp.). Gonzalez confirmed the price and represented that he could get the tests within the week. (Id.); (WhatsApp Messages at 47–48, Ex. 3 to Resp., ECF No. 65-4). On

October 22, Americare sent an invoice for 59,520 “Flowflex Antigen OTC” tests for $476,160 payable upon receipt. (Oct. 22 Invoice, Ex. 3 to Mot. Summ. J., ECF No. 62-3). Americare contracted with GHS to buy the tests at $7 per test for a total purchase price of $416,640. (Gonzalez Decl. ¶ 8, Ex. 1 to Resp.). The tests from GHS arrived in late November and Gonzalez met with a GHS representative at a warehouse to receive them. (Id. ¶ 9). Gonzalez noticed that the tests kits were marked as “CE” and were in blue boxes with white stickers stating “For use under Emergency Use Authorization (EUA) only.” (Id.); (Resp. to Request for Admission, Ex. 12 to Mot. Summ. J., ECF No. 62-12); (Photographs of Subject Test, Ex. 6 to Mot. Summ. J., ECF No. 62-6). When Gonzalez asked about the stickers, the representative assured him that the tests were fully approved as EUA in the United States and showed him a FDA letter purporting as much. (Gonzalez Decl. ¶ 10, Ex. 1 to Resp.). Gonzalez called Goldsmith, showed him the stickers on the boxes, and asked how he wanted to proceed. (Id. ¶ 11). Goldsmith approved the delivery and instructed Gonzalez to rush the tests to Maryland. (Id.). Americare drop-shipped the COVID-19 tests to warehouses beginning November 24, 2021. (Goldsmith Decl. ¶ 7, Ex. 1 to Mot. Summ. J.). On January 9, 2022, ACON Laboratories issued a press release explaining that there were two types of Flowflex COVID-19 tests, but that only one of them was approved for sale in the United States. (Acon Press Release, Ex. 7 to Mot. Summ. J., ECF No. 62-7). The Flowflex COVID-19 Antigen Home Tests (white box) were approved, but the Flowflex SARS-CoV-2 Antigen Rapid Tests (blue box) were not. (Acon Press Release, Ex. 7 to Mot. Summ. J., ECF No. 62-7). On the same day, the FDA issued a recall for the CE blue-box tests. (FDA Recall, Ex. 8 to Mot. Summ. J., ECF No. 62-8). This is where the conflict arises. GHS emailed Gonzalez details about the approved white-box tests, which was the email that Gonzalez forwarded to Goldsmith. (Kasbee Email, Ex. 2 to Resp., ECF No. 65-2). So, it appears that

both Americare and Elevation expected to receive the approved white-box tests. But the tests that GHS sent, and Americare then shipped to Elevation, were the blue-box tests. A week after the recall, Goldsmith sent Gonzalez a message stating that the Flowflex tests were “blue boxed and no good.” (WhatsApp Messages at 59, Ex. 3 to Resp.). When Gonzalez replied that he didn’t know there was a problem with the tests, Goldsmith wrote that perhaps GHS had lied to Americare or were also lied to themselves. (Id.). The next day, Goldsmith messaged, “All the tests you supplied were CE!” “This was fraud bro,” and “I never ordered CE.” (Id.). Gonzalez insisted that he had no idea because the boxes said they were EUA authorized, and Goldsmith responded that this was “now a legal issue.” (Id.). Gonzalez offered to replace the blue-box tests with approved white-box tests and asked Goldsmith to send back the blue-box tests. (Id. at 60–61). Goldsmith said that he would not return the tests because the FDA instructed for them to be disposed of. (Id.); (Gonzalez Decl. ¶¶ 19–21, Ex. 1 to Resp.). Goldsmith also declined to provide proof that the tests were actually destroyed. (Id.). Gonzalez reminded Goldsmith that he called him when the tests arrived in his warehouse, showed him the blue-box tests, and that Goldsmith agreed they should be shipped. (WhatsApp Messages at 64, Ex. 3 to Resp.). Goldsmith asserted for the first time that he never saw the goods. (Id.). Because Goldsmith did not return the tests or provide proof they were disposed of, GHS and Americare did not replace the blue-box tests. (Gonzalez Decl. ¶ 21, Ex. 1 to Resp.). Elevation acquired replacement tests from a different supplier. (Goldsmith Decl. ¶ 13, Ex. 1 to Mot. Summ. J.). According to Elevation, Americare has refused to accept a return of the blue-box COVID-19 tests. (Id. ¶ 15). In September 2022, Elevation initiated the instant action against Americare, Gonzalez, and Mrs. Gonzalez. (Compl., ECF No. 1). Americare filed an Answer and brought Counterclaims against Elevation. (Ans., ECF No. 12). Americare also filed a Third-Party

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Elevation Health LLC v. Americare, Inc., (D. Nev. 2024).

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