Bubak v. GOLO, LLC

CourtDistrict Court, E.D. California
DecidedJanuary 8, 2024
Docket1:21-cv-00492
StatusUnknown

This text of Bubak v. GOLO, LLC (Bubak v. GOLO, LLC) is published on Counsel Stack Legal Research, covering District Court, E.D. California primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Bubak v. GOLO, LLC, (E.D. Cal. 2024).

Opinion

1 2 3 4 5 6 7 8 UNITED STATES DISTRICT COURT 9 FOR THE EASTERN DISTRICT OF CALIFORNIA 10 11 VINCENZZA BUBAK, No. 1:21-cv-00492-DAD-AC 12 Plaintiff, 13 v. ORDER GRANTING MOTION FOR RECONSIDERATION, GRANTING 14 GOLO, LLC, DEFENDANT’S MOTION TO DISMISS PLAINTIFF’S REMAINING CLAIMS, AND 15 Defendant. DENYING DEFENDANT’S MOTION TO STAY AS HAVING BEEN RENDERED 16 MOOT

17 (Doc. Nos. 44, 45)

18 19 This matter is before the court on defendant’s motion for reconsideration of the court’s 20 order dated August 29, 2022 (Doc. No. 38) and defendant’s motion to stay proceedings in this 21 case pending the court’s resolution of the motion for reconsideration. (Doc. Nos. 44, 45.) On 22 October 24, 2023, defendant’s motions were taken under submission to be decided on the papers. 23 (Doc. No. 64.) For the reasons discussed below, the court will grant defendant’s motion for 24 reconsideration of the undersigned August 29, 2022 order, grant defendant’s motion to dismiss 25 plaintiff’s sole remaining claims, and deny defendant’s motion to stay this case as moot. 26 BACKGROUND 27 In the operative first amended complaint (“FAC”), plaintiff brings three state law 28 claims—violation of California’s Unfair Competition Law (“UCL”), False Advertising Law 1 (“FAL”), and Consumer Legal Remedies Act (“CLRA”)—against defendant GOLO, LLC, a 2 dietary supplement distributor who allegedly misrepresented its “Release Supplement” product 3 (“Release”). (Doc. No. 17.) In the FAC, plaintiff had asserted three theories of liability in 4 support of these claims: (i) defendant makes implied disease claims without meeting the 5 premarket approval requirements of the Food, Drug, and Cosmetic Act (“FDCA”), 21 U.S.C. 6 §§ 301, et seq.; (ii) defendant provides inadequate directions for use under an FDCA drug rule; 7 and (iii) defendant has an insufficient basis upon which to claim that Release is “clinically 8 proven.” (Id. at 3–7.) 9 On July 20, 2021, defendant filed a motion to dismiss all three claims under all three 10 theories. (Doc. No. 18.) Therein, defendant argued, inter alia, that plaintiff’s claims under the 11 first theory—“implied disease claims”—are preempted as a matter of law by the FDCA. (Doc. 12 No. 18-1 at 9.) 13 On August 29, 2022, the court issued an order granting in part and denying in part 14 defendant’s motion to dismiss.1 (Doc. No. 38.) Specifically, the court granted defendant’s 15 motion as to plaintiff’s claims under the second and third theories of liability but denied 16 defendant’s motion to dismiss plaintiff’s claims under the “implied disease claims” theory 17 because “plaintiff’s UCL, FAL, and CLRA claims premised on alleged violations of California’s 18 Sherman Law are not preempted by the FDCA.” (Id. at 16, 25.) The court concluded that 19 plaintiff’s state law claims were not preempted “[b]ecause plaintiff brings her claims under 20 California’s Sherman Law, which parallels the federal law requirements and provides for private 21 ///// 22 ///// 23 ///// 24 1 The court’s August 29, 2022 order summarized the FAC’s allegations, the parties’ respective 25 arguments, and the FDCA and its regulations. (Doc. No. 38 at 2–4, 6–16.) Rather than repeat that summary in this order, the court incorporates it by reference herein. In addition, that order 26 also reassigned this case to a then-recently confirmed district judge. (Id. at 36.) On September 27 13, 2023, the case was again reassigned to a district judge sitting in the district’s Sacramento Courthouse. (Doc. No. 60.) On October 23, 2023, the case was reassigned to the undersigned, 28 now also sitting in Sacramento. (Doc. No. 63.) 1 enforcement.”2 (Id. at 13–14.) The court explained that “[t]his conclusion is in line with the 2 generally accepted principle that a plaintiff bringing such a parallel state law claim must be suing 3 for conduct that violates the FDCA, but must not be suing because the conduct violates the 4 FDCA, as such a claim would be impliedly preempted under Buckman Co. v. Plaintiff’s Legal 5 Comm., 531 U.S. 341 (2001).” (Id. at 14–15.) 6 On September 21, 2022, defendant filed the pending motion for reconsideration of the 7 part of the court’s August 29, 2022 order that denied defendant’s motion to dismiss plaintiff’s 8 “implied disease claims” and rejected defendant’s arguments that those claims are preempted by 9 the FDCA. (Doc. No. 44.) In the pending motion, defendant explains that it is moving “for 10 reconsideration because the Ninth Circuit’s recent decision in Nexus Pharmaceuticals, Inc. v. 11 Central Admixture Pharmacy Services, Inc., [48 F.4th 1040] (9th Cir. Sept. 13, 2022), decided 12 shortly after the Court’s Order, provides an intervening clarification in the controlling law and 13 confirms that plaintiff’s implied disease claim is preempted under the [FDCA] and should be 14 dismissed.” (Id. at 9.) Defendant also requests in the alternative that if reconsideration is denied, 15 the court certify the August 29, 2022 for interlocutory appeal pursuant to 28 U.S.C. § 1292(b). 16 (Id.) 17 Also on September 21, 2022, defendant filed a motion to stay proceedings in this case 18 pending resolution of its motion for reconsideration. (Doc. No. 45.) 19 On October 26, 2022, plaintiff filed oppositions to both pending motions. (Doc. Nos. 53, 20 54.) On November 7, 2022, defendant filed its replies thereto. (Doc. Nos. 55, 56.) 21 On October 24, 2023, defendant filed a notice of supplemental authority to notify the 22 court of one Ninth Circuit decision and four California district court decisions, all of which cited 23 the Nexus opinion and dismissed state law claims as preempted by the FDCA. (Doc. No. 65.) 24 ///// 25 ///// 26 2 As noted in the court’s August 29, 2022 order, the Sherman Law incorporates the FDA 27 regulations and adopts them as the law of California. (Doc. No. 38 at 13) (citing Cal. Health & Safety Code § 110100(a) (“All food labeling regulations . . . adopted pursuant to the federal act . . 28 . shall be the food labeling regulations of this state.”)). 1 LEGAL STANDARD 2 Rule 54(b) of the Federal Rules of Civil Procedure provides that “any order or other 3 decision, however designated, that adjudicates fewer than all the claims . . . does not end the 4 action as to any of the claims . . . and may be revised at any time before the entry of a judgment 5 adjudicating all the claims . . . .” Fed. R. Civ. P. 54(b). In contrast, Rule 60(b) provides that 6 “[o]n motion and just terms, the court may relieve a party or its legal representative from a final 7 judgment, order, or proceeding,” for certain reasons. Fed. R. Civ. P. 60(b) (emphasis added). In 8 its pending motion for reconsideration, defendant does not refer to any particular rule of the 9 Federal Rules of Civil Procedure under which it seeks reconsideration. Because the court’s 10 August 29, 2022 order granting in part and denying in part defendant’s motion to dismiss 11 plaintiff’s FAC is interlocutory and not final, Rule 54(b) provides the proper basis for possible 12 reconsideration of that order. 13 The Ninth Circuit has “long recognized ‘the well-established rule that a district judge 14 always has power to modify or to overturn an interlocutory order or decision while it remains 15 interlocutory.’” Credit Suisse First Bos. Corp. v.

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Bubak v. GOLO, LLC, Counsel Stack Legal Research, https://law.counselstack.com/opinion/bubak-v-golo-llc-caed-2024.