Pizana v. Sanmedica International LLC

District Court, E.D. California·Decided February 1, 2021·No. 1:18-cv-00644·Unknown

Opinion

1 2 3 UNITED STATES DISTRICT COURT 4 FOR THE EASTERN DISTRICT OF CALIFORNIA 5 6 RAUL PIZANA, individually and on No. 1:18-cv-00644-DAD-SKO behalf of all others similarly situated, 7 ORDER ON DEFENDANT’S MOTION TO Plaintiff, PARTIALLY QUASH OR MODIFY 8 SUBPOENA TO THE FEDERAL TRADE v. COMMISSION 9 SANMEDICA INTERNATIONAL, LLC, (Doc. 113) 10 and DOES 1 through 10, inclusive,

11 Defendants. 12 13 This matter is before the Court on Defendant SanMedica International, LLC 14 (“Defendant”)’s “Motion to Partially Quash or Modify Subpoena to the Federal Trade 15 Commission” (the “Motion to Quash”). (Doc. 113.) Defendant and Plaintiff Raul Pizana 16 (“Plaintiff”) filed their joint statement directed to the Motion to Quash (the “Joint Statement”), as 17 required by this Court’s Local Rule 251, on December 30, 2020. (Doc. 126.) The Court reviewed 18 the parties’ papers and all supporting material and found the matter suitable for decision without 19 oral argument. The hearing set for January 6, 2021, was therefore vacated. (Doc. 129.) 20 Having considered the Joint Statement and its exhibits, and for the reasons set forth below, 21 Defendant’s Motion to Quash will be construed as a motion for a protective order pursuant to 22 Federal Rules of Civil Procedure 26(c) and granted in part and denied in part. 23 I. BACKGROUND 24 Plaintiff filed this putative class action on May 9, 2018, challenging the advertising and 25 efficacy of SeroVital-hgh (the “Product”), a purported Human Growth Hormone (“HGH”) 26 supplement produced by Defendant that was purchased by Plaintiff in early 2017. (Doc. 53, 27 Second Am. Compl. (“SAC”) at ¶¶ 1, 6, 9.) The Second Amended Complaint, filed on November 28 13, 2019, asserts three causes of action: (1) a violation of California Civil Code § 1750, et. seq., 1 the Consumer Legal Remedies Act (“CLRA”); (2) a violation of California Business & Professions 2 Code § 17500, et. seq., the False Advertising Law (“FAL”); and (3) a violation of California 3 Business & Professions Code § 17200, et. seq., the Unfair Competition Law (“UCL”). (SAC at 4 ¶¶ 60–121.). 5 The crux of Plaintiff’s suit is that Defendant’s Product, despite being marketed as an HGH 6 supplement that can “make users look and feel decades—not years, but DECADES—younger,” is 7 “no more effective for its advertised purposes than a placebo[] and is therefore worthless to 8 California consumers[.]” (SAC at ¶¶ 1–5.) Specifically, Plaintiff alleges: 9 (1) [T]he Product cannot increase HGH levels whatsoever, let alone by 682%; (2) the Product does not reduce wrinkles, “decrease[] body fat,” “increase[] lean 10 muscle mass,” strengthen bones, “improve[] mood,” “heighten[] sex drive,” or make “users look and feel decades … younger” because the oral administration of 11 amino acids like SeroVital does not increase growth hormone bioactivity; (3) there is no causal link between increased HGH levels and most of the claimed uses, 12 including wrinkle reduction, increased lean muscle mass, stronger bones, improved mood, [or] heightened sex drive; and (4) if SeroVital were to increase HGH levels 13 as claimed, it would cause significant health risks. 14 (Id. at ¶ 2.) 15 Plaintiff seeks to assert claims on behalf of a proposed class defined as: 16 All persons residing in California who purchased the Product for personal use and not for resale during the time period May 9, 2014, through the present. Excluded 17 from the Class are Defendant’s officers, directors, and employees, and any individual who received remuneration from Defendant in connection with that 18 individual’s use or endorsement of the Product. 19 (SAC ¶ 50.) On March 6, 2020, the Court entered a scheduling order that bifurcated merits from 20 class certification discovery and set a deadline of December 18, 2020, for class discovery only.1 21 (See Doc. 74.) 22 On December 2, 2020, Plaintiff served a subpoena (the “Subpoena”) on the Federal Trade 23 Commission (“FTC”), requesting ten categories of documents pertaining to Defendant and ten 24 other non-party companies, collectively referred to as the “Basic Research Enterprise,” and the 25 Product and two other products (Growth Factor-9 (“GF-9”) and Thrive-hgh) not identified in the 26 27 1 The parties agreed in their joint scheduling report that discovery in this case should be bifurcated. (See Doc. 71 at 28 5.) 1 SAC.2 3 (See Doc. 126-1 at 7–8, 13–14.) On December 11, 2020, Defendant filed the instant 2 motion. (Doc. 113.) 3 II. LEGAL STANDARDS 4 A. Discovery Generally 5 Federal Rule of Civil Procedure 26(b)(1) provides that parties 6 [m]ay obtain discovery regarding any nonprivileged matter that is relevant to any party’s claim or defense and proportional to the needs of the case, considering the 7 importance of the issues at stake in the action, the amount in controversy, the parties relative access to relevant information, the parties’ resources, the importance of the 8 discovery in resolving the issues, and whether the burden or expense of the proposed discovery outweighs its likely benefit. 9 10 Fed. R. Civ. P. 26(b)(1). 11 Motions for protective orders are governed by Rule 26(c), which states in relevant part: 12 A party or any person from whom discovery is sought may move for a protective order in the court where the action is pending[.] The motion must include a 13 certification that the movant has in good faith conferred or attempted to confer with other affected parties in an effort to resolve the dispute without court action. The 14 court may, for good cause, issue an order to protect a party or person from 15 annoyance, embarrassment, oppression, or undue burden or expense[.] 16 Fed. R. Civ. P. 26(c). District courts have broad discretion to determine whether a protective order 17 is appropriate and, if so, what degree of protection is warranted. Seattle Times Co. v. Rhinehart, 18 467 U.S. 20, 36 (1984); see also Phillips ex rel. Estates of Byrd v. Gen. Motors Corp., 307 F.3d 19 1206, 1211–12 (9th Cir. 2002). The party seeking to limit discovery has the burden of proving 20 “good cause,” which requires a showing “that specific prejudice or harm will result” if the 21 protective order is not granted. In re Roman Catholic Archbishop of Portland in Oregon, 661 F.3d 22 417, 424 (9th Cir. 2011) (citing Foltz v. State Farm Mut. Auto. Ins. Co., 331 F.3d 1122, 1130 (9th 23 Cir. 2003)).

24 2 On December 23, 2020, Plaintiff filed a motion for leave to file a third amended complaint (Doc. 118), which is 25 pending. The motion seeks to amend the operative complaint to add: as defendants the ten other companies that are part of the Basic Research Enterprise; as plaintiffs other persons who have purchased the Product, GF-9, Thrive-hgh, or SeroDyne in California within the past three years; and claims alleging a violation of the Racketeer Influenced and 26 Corrupt Organizations (“RICO”) Act, 18 U.S.C. § 1962(a), (c)–(d), and mail and wire fraud, 18 U.S.C. §§ 1341, 1343. (See Doc. 118.) 27 3 In June 2004, the FTC commenced an administrative action against some of the constituent companies of the Basic Research Enterprise for false advertising, and the action resolved about two years later via a consent agreement, which 28 is still in effect. (See Doc. 126 at 10–11; Doc.

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