Lenco Diagnostic Laboratories, Inc. v. McKinley Scientific, Inc.

CourtDistrict Court, E.D. New York
DecidedJuly 7, 2020
Docket1:15-cv-01435
StatusUnknown

This text of Lenco Diagnostic Laboratories, Inc. v. McKinley Scientific, Inc. (Lenco Diagnostic Laboratories, Inc. v. McKinley Scientific, Inc.) is published on Counsel Stack Legal Research, covering District Court, E.D. New York primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Lenco Diagnostic Laboratories, Inc. v. McKinley Scientific, Inc., (E.D.N.Y. 2020).

Opinion

UNITED STATES DISTRICT COURT EASTERN DISTRICT OF NEW YORK -------------------------------------------------------X LENCO DIAGNOSTIC LABORATORIES, INC.,

Plaintiff, MEMORANDUM AND ORDER -against- 15 CV 1435 (FB)(RML) MCKINLEY SCIENTIFIC, INC.,

Defendant. --------------------------------------------------------X LEVY, United States Magistrate Judge: Plaintiff Lenco Diagnostic Laboratories, Inc. (“plaintiff” or “Lenco”) moves for leave to amend its Second Amended Complaint to add an alternative claim for breach of contract. Defendant McKinley Scientific, Inc. (“defendant” or “McKinley”), the only remaining defendant in this case, opposes the motion. I heard oral argument on November 22, 2019.1 For the reasons stated below, plaintiff’s motion is granted. BACKGROUND AND PROCEDURAL HISTORY Familiarity with the prior proceedings is assumed. Briefly, plaintiff, a clinical laboratory based in Brooklyn, New York, commenced this diversity action on March 18, 2015. It alleges, inter alia, that McKinley, a New Jersey company that acts as a selling agent for new and used laboratory equipment, made false representations to plaintiff regarding its ability to assist plaintiff with developing and certifying a mass spectrometry (“MS”) toxicology testing

1 A few days after the oral argument, the parties advised that they were willing to engage in court-annexed mediation. I referred the case to mediation on November 30, 2019, and the parties selected a mediator on December 16, 2019. After receiving extensions of time, the parties completed mediation on June 16, 2020, reporting to the court that they were unable to resolve this case. operation in accordance with New York State Department of Health (“DOH”) procedures. (See Complaint, dated Mar. 18, 2015 (“Compl.”), Dkt. No. 1; Second Amended Complaint, dated Oct. 3, 2018 (“Second Am. Compl.”), Dkt. No. 74.) Lenco claims to be “one of the largest independent clinical labs in the region, with well over 100 employees, offering a full range of

diagnostic services to doctors, hospitals and individual patients.” (Second Am. Compl. ¶ 22.) In 2012, “Lenco decided to add clinical toxicology to its expanding menu of diagnostic services” and thus “needed to purchase MS equipment, consisting of numerous pieces of advance technology machinery integrated with software as well as the necessary supplies, additional staff and support services.” (Id. ¶ 23.) Plaintiff explains that MS is a “testing procedure that helps identify the amount and type of chemicals present in a sample by measuring the mass-to-charge ratio and abundance of gas-phase ions.” (Id. ¶ 24.) MS is “a highly complex testing process, involving sophisticated equipment and protocols that enable labs to test for chemical substances in, among other things, urine and blood—with accuracy and sensitivity significantly greater than with other, older testing procedures.” (Id. ¶ 25.)

In addition, according to plaintiff, MS is “a heavily regulated field of diagnostics” and “each state has developed its own regulations and procedures governing certification of labs for MS testing.” (Id. ¶ 26.) In New York, the DOH “is responsible for quality review and certification of all clinical labs, including with respect to MS testing.” (Id. ¶ 27.) The DOH’s certification procedure “is a multi-step process requiring a lab . . . seeking to engage in MS testing to: (i) provide a set of accurate, reproducible and scientifically robust instructions for MS testing of laboratory samples, commonly referred to as “methods;” (ii) validate these methods internally through a series of scientific experiments, patient sample simulations as well as data collection and analysis, commonly referred to as “Method Validation”; and (iii) submit these methods and the standard operating procedure manuals (“SOPM”) to DOH for review and approval.” (Id. ¶ 28.) Labs “are further required to conduct proficiency tests (hereinafter “Proficiency Testing”) on simulated patient samples provided by DOH and report the results to DOH, which judges the accuracy of these results in determining whether to provide the lab with

the appropriate license.” (Id. ¶ 29.) Because Lenco “had neither the necessary in-house expertise nor sufficient resources” to carry out these requirements, it alleges that it sought out a “turn-key” toxicology operation. (Id. ¶ 30.) Lenco claims that between January and March 2012, Martin Steel, a senior executive at McKinley, repeatedly represented to it that McKinley “was going to be able to deliver precisely the type of ‘turn-key’ operation Lenco was looking for.” (Id. ¶¶ 31-32.) Lenco alleges that on March 15, 2012, it paid McKinley $608,890 for equipment and services, including: (1) three refurbished “Thermo TSQ Quantum Ultra” machines (“MS Machines”); (2) two “Peak Scientific N2” generators (“Generators”); (3) numerous pieces of supporting equipment; and (4) comprehensive consulting and technical support services

necessary to assist Lenco in launching toxicology diagnostics. (Id. ¶¶ 37-38.) One year later, on March 11, 2013, Lenco paid McKinley $531,021 for more MS equipment and services, including three refurbished MS Machines, two new Generators, various items of supporting equipment, and comprehensive consulting and technical support services on that additional equipment. (Id. ¶¶ 64-66.) According to the Second Amended Complaint, Lenco failed its initial Proficiency Tests with DOH in March 2013, at approximately the time of its second purchase of equipment and services. (Id. ¶ 69.) Despite McKinley’s assurances that this was a “minor setback,” Lenco claims that it eventually determined that “the entire package of equipment and services purchased by Lenco was riddled with so many deficiencies and shortcomings as to be totally unusable.” (Id. ¶ 82.) Ultimately, “Lenco came to believe that the MS Machines it had purchased from McKinley were utterly unsuitable for the only purpose Plaintiff needed them – i.e. to run a high-volume commercial MS diagnostic service in a clinical setting.” (Id. ¶ 93.)

In the Second Amended Complaint, plaintiff asserted claims for fraud, conspiracy, and unjust enrichment. (See generally id.) It now moves to amend its complaint again to add an “alternative” claim for breach of contract. It has submitted a proposed Third Amended Complaint. (See Declaration of Joshua M. Lurie, Esq., dated Sept. 20, 2019, Dkt. No. 96, Ex. A.) Defendant opposes the motion, arguing that plaintiff delayed in seeking to amend after representing that it did not intend to pursue a contract theory. (Defendant’s Brief in Opposition to Plaintiff’s Motion to Amend the Complaint, dated Sept. 30, 2019 (“Def.’s Mem.”), Dkt. No. 98, at 1.) Defendant also argues that the proposed amendment should be denied because it is not based on any newly-discovered facts, the last-minute change in litigation strategy would prejudice defendant and lead to additional discovery and delays, and the

amendment would be futile. (See id.) I will address defendant’s arguments in turn. DISCUSSION A. Legal Standard Federal Rule of Civil Procedure 15(a) provides that leave to amend a complaint “should [be] freely give[n] . . . when justice so requires.” FED. R. CIV. P. 15(a). In Foman v. Davis, the Supreme Court set out the standard for motions to amend: “In the absence of any apparent or declared reason—such as undue delay, bad faith or dilatory motive on the part of the movant, repeated failure to cure deficiencies by amendments previously allowed, undue prejudice to the opposing party by virtue of allowance of the amendment, futility of amendment, etc.—the leave sought should, as the rules require, be ‘freely given.’” Foman v. Davis, 371 U.S. 178, 182 (1962). B.

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Bluebook (online)
Lenco Diagnostic Laboratories, Inc. v. McKinley Scientific, Inc., Counsel Stack Legal Research, https://law.counselstack.com/opinion/lenco-diagnostic-laboratories-inc-v-mckinley-scientific-inc-nyed-2020.