In re Lyman Good Dietary Supplements Litigation

CourtDistrict Court, S.D. New York
DecidedJune 22, 2020
Docket1:17-cv-08047
StatusUnknown

This text of In re Lyman Good Dietary Supplements Litigation (In re Lyman Good Dietary Supplements Litigation) is published on Counsel Stack Legal Research, covering District Court, S.D. New York primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
In re Lyman Good Dietary Supplements Litigation, (S.D.N.Y. 2020).

Opinion

UNITED STATES DISTRICT COURT DATE FILED: 6/22/2 020 SOUTHERN DISTRICT OF NEW YORK -------------------------------------------------------------- X : 17-CV-8047 (VEC) In re Lyman Good Dietary Supplements Litigation : : OPINION AND ORDER -------------------------------------------------------------- X VALERIE CAPRONI, United States District Judge: This action stems from Plaintiff Lyman Good’s suspension from the Ultimate Fighting Championship (“UFC”) after testing positive for 1-androstenedione (“1-A”), an illicit anabolic steroid. Plaintiff claims that Anavite, a dietary supplement sold and manufactured by Defendants, contained 1-A and caused his positive drug test and resulting suspension. Plaintiff asserts claims for: (i) breach of express warranty; (ii) breach of implied warranties; (iii) violations of New York General Business Law §§ 349-50; (iv) products liability under strict liability and negligence theories; and (v) general negligence. See Second Am. Compl. (“SAC”), Dkt. 60. Defendants have moved for summary judgment on all claims pursuant to Federal Rule of Civil Procedure 56. Dkt. 126. For the following reasons, Defendants’ motion is GRANTED. BACKGROUND1 Plaintiff is a professional mixed martial arts fighter who has competed in the UFC since July 2015. Defs.’ 56.1 Stmt. ¶ 1. The UFC subjects its athletes to a performance enhancing drug (“PED”) monitoring program overseen by the United States Anti-Doping Agency (“USADA”). Id. ¶ 2. As part of his contract with the UFC, Plaintiff agreed to submit to random PED tests 1 All facts described herein are undisputed unless otherwise stated. The Court will refer to the parties’ submissions as follows: Defendants’ Memorandum of Law in support of their motion for summary judgment, Dkt. 126-1, as “Defs.’ Mem. of Law”; Defendants’ Local Civil Rule 56.1 Statement of Undisputed Facts, Dkt. 126- 2, as “Defs.’ 56.1 Stmt.”; the Declaration of David Marck in support of Defendants’ motion, Dkt. 126-3, as “Marck Decl.”; Plaintiff’s Memorandum of Law in Opposition to Defendants’ Motion, Dkt. 129, as “Pl. Mem. of Law”; Plaintiff’s Statement of Material Facts in Dispute Pursuant to Local Civil Rule 56.1, Dkt. 128, as “Pl. 56.1 Stmt.”; Defendants’ Response to Plaintiff’s Additional Factual Allegations, Dkt. 130-1, as “Defs.’ 56.1 Resp. Stmt.” administered by the USADA. Id. ¶ 3. On October 14, 2016, Plaintiff took a PED test; on October 24, 2016, the lab results revealed that Plaintiff had tested positive for 1-A and its metabolite 1-(5α)-androsten-3α-o1-17-one.2 Id. ¶¶ 4-5; Marck Decl., Ex. 1. 1-A is a banned PED and its presence in Plaintiff’s urine would typically result in suspension from the UFC. Id.

¶ 6. Indeed, after Plaintiff tested positive for 1-A, the USADA suspended him for two years; his suspension was later reduced to six months. Pl. 56.1 Stmt. ¶ 42. At some point before his drug test in October 2016, Plaintiff claims he consumed Anavite, a multivitamin sold and manufactured by Defendants.3 Id. ¶¶ 35-36; Defs.’ 56.1 Stmt. ¶ 7. Although it does not appear as an ingredient on the vitamin’s label, Plaintiff alleges that Anavite contains 1-A, and that it was his consumption of Anavite that caused him to test positive for 1-A. Defs.’ 56.1 Stmt. ¶ 7. Prior to submitting his urine sample to the USADA for testing, Plaintiff completed a “Declaration of Use,” setting forth the “prescription/non-prescription medications, any infusions and/or injections, dietary supplements and/or other substances taken in the last seven (7) days (including: vitamins, minerals, herbs, proteins, amino acids, and any

other dietary supplements).” Id. ¶ 24; Marck Decl. Ex. 8. The declaration required Plaintiff to certify that he had reviewed the substances listed on the declaration and to confirm that it was complete and accurate. Defs.’ 56.1 Stmt. ¶ 25. Plaintiff did not list Anavite on his USADA declaration, although he did list over a dozen other dietary supplements, including another

2 1-androstenedione (or 1-A) is the common name for “5α-1-androstene-3,17-dione,” which is an androstane analog with an α-bonded hydrogen on carbon 5, a double bond between carbons 1 and 2, and double-bonded oxygens at carbons 3 and 17. Defs.’ 56.1 Stmt. at ¶ 8; Marck Decl. Ex. 2 at ¶ 32 (Expert Report of Steve J. Bannister, Ph.D., dated December 7, 2018). 1-A is not produced by the human body; in order to be detected in Plaintiff’s urine, he had to have ingested it. Defs.’ 56.1 Stmt. ¶ 9.

3 It is not entirely clear when Plaintiff began taking Anavite. See Defs.’ 56.1 Resp. Stmt. ¶ 36. In his deposition, when asked about the last time he took Anavite before his drug test on October 14, 2016, he answered “I don’t remember.” Id.; Dkt. 105-5 at 319:17-25. Similarly, when asked how long he had been taking Anavite before October 14, 2016, Plaintiff responded, “I don’t remember.” Dkt. 105-5 at 337:14-17. multivitamin. Id. ¶¶ 26-27. Moreover, at no point while his drug test results were pending did Plaintiff inform the USADA that his declaration was inaccurate or incomplete. Id. ¶ 28. In 2017, well after Plaintiff’s positive PED test, the USADA submitted to the Sports Medicine Research and Testing Laboratory (“SMRTL”) two bottles of Anavite for testing. Id. ¶

13. One bottle was open and contained a single tablet; the other bottle was unopened and contained 180 tablets. Dkt. 96-5 at 3, 6. Both purported to be from the same lot. Id. USADA asked SMRTL to analyze the tablets for anabolic agents.4 Id.; Defs.’ 56.1 Stmt. ¶ 13. On March 29, 2017, the SMRTL emailed the results of its analyses to the USADA. Dkt. 96-5 at 2. The SMRTL report contains two pages; the first states that 1-A was detected in Anavite from one bottle at “approximately 370 nanograms per tablet” and the second page states that 1-A was detected in Anavite from the second bottle at “approximately 850 nanograms per tablet.”5 Id. at 3, 6. There is no explanation for why tablets from the same lot would contain radically different quantities of 1-A. Plaintiff asserts claims for: (i) breach of express warranty; (ii) breach of implied warranty

of merchantability; (iii) breach of implied warranty of fitness for a particular purpose; (iv) violations of New York General Business Law §§ 349-50; (v) products liability under strict liability and negligence theories; and (vi) general negligence. See SAC, Dkt. 60.

4 The Court notes, however, that neither bottle of Anavite tested by SMRTL was the bottle from which Plaintiff claims to have consumed Anavite in 2016; Plaintiff failed to preserve the bottle of Anavite from which he was supposedly taking tablets prior to his PED test in October 2016. See Dkt. 122.

5 Defendants note that none of the other four laboratories that analyzed Anavite detected 1-A. Defs.’ Mem. of Law at 8 (citing Dkt. 96 at 7). Moreover, Plaintiff’s reference to the lab results from LGC Science, Inc., see Pl. 56.1 Stmt. ¶ 38, is irrelevant. Although LGC Science detected androstenedione and DHEA in Anavite, LGC Science did not detect 1-A. As this Court explained in its ruling on Defendants’ motion to exclude Plaintiff’s proposed expert testimony, 1-A, androstenedione, and DHEA are all distinct substances. See Dkt. 125 at 9. It is undisputed that “Plaintiff did not fail his PED test due to an overabundance of androstenedione. Rather, he failed his PED test because USADA’s lab detected 1-androstenedione” in his urine. Defs.’ 56.1 Stmt. ¶ 12. DISCUSSION Summary judgment is appropriate when “the movant shows that there is no genuine dispute as to any material fact and the movant is entitled to judgment as a matter of law.” Fed. R. Civ. P. 56(a); see also Celotex Corp. v.

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Bluebook (online)
In re Lyman Good Dietary Supplements Litigation, Counsel Stack Legal Research, https://law.counselstack.com/opinion/in-re-lyman-good-dietary-supplements-litigation-nysd-2020.