Dominic Little et al v. USPLabs LLC et al

Filing 31

ORDER GRANTING PLAINTIFFS MOTION TO REMAND 12 ;Defendants pending motion to dismiss 10 is DENIED AS MOOT 12 by Judge Dean D. Pregerson. cc: order, docket, remand letter to Los Angeles Superior Court No.BC 534065. ( MD JS-6. Case Terminated ) (Attachments: # 1 rmdltr). (lc). Modified on 4/25/2014 (lc).

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1 2 O 3 4 5 6 7 8 UNITED STATES DISTRICT COURT 9 CENTRAL DISTRICT OF CALIFORNIA 10 11 DOMINIC LITTLE, et al, 12 Plaintiffs, 13 v. 14 USPLABS LLC, et al., 15 Defendants. ___________________________ ) ) ) ) ) ) ) ) ) ) Case No. CV 14-01540 DDP (SHx) ORDER GRANTING PLAINTIFFS’ MOTION TO REMAND [DKT. NO. 12] 16 17 Presently before the Court is Plaintiffs’ motion to remand 18 this action (the “Motion”). (Docket No. 12.) For the reasons stated 19 in this Order, the Motion is GRANTED. The action is remanded, and 20 Defendants’ pending motion to dismiss (Docket No. 10) is DENIED AS 21 MOOT. 22 I. Background 23 Plaintiffs are twelve individuals. Plaintiffs allege that each 24 of them used one of two dietary supplements, Jack3d and OxyElite, 25 for some period of time. (Complaint, Docket 1-1, ¶¶ 28-83.) Jack3d 26 and OxyElite both contain a chemical know as DMAA. (Id. ¶ 90.) DMAA 27 is a sympathomimetic drug, a class of drug used by physicians to 28 increase blood pressure and constrict blood vessels, but also 1 widely used because of their perceived ability to enhance athletic 2 performance. (Id. ¶¶ 91-92.) Plaintiffs allege that DMAA can cause 3 dangerous cardiovascular events, such as heart attack, stroke, 4 arrhythmia, heart palpitations, dizziness, cardiac arrest, and 5 death, as well as other serious adverse effects, including liver 6 failure, kidney failure, and seizures. (Id. ¶ 4.) Each Plaintiff 7 alleges that one or more of these serious harms happened to him or 8 her as a result of the use of Jack3d or OxyElite. (Id. ¶¶ 28-83.) 9 Plaintiffs allege that Defendants in this action each 10 designed, formulated, marketed, distributed, and/or sold Jack3d and 11 OxyElite products containing DMAA, despite its inherent dangers. 12 (Id. ¶ 87.) Plaintiffs allege that various misrepresentations were 13 made in the marketing of Jack3d and OxyElite regarding the 14 products’ safety and safety testing. (Id. ¶¶ 97-113.) Further, 15 Plaintiffs allege that Jack3d and OxyElite are ineffective for 16 their advertised uses. (Id. ¶ 88.) Plaintiffs bring the following 17 state law claims arising out of these facts: (1) negligence; (2) 18 strict products liability for design defects; (3) strict products 19 liability for failure to warn; (4) breach of express warranty; (5) 20 breach of implied warranty; and (6) unlawful business practices in 21 violation of Cal. Bus. & Prof. Code § 17200 et seq. As factual 22 support for their allegations, Plaintiffs describe various warnings 23 and communications issued by the Food and Drug Administration 24 (“FDA”) regarding DMAA and Defendants’ use of DMAA in their 25 products. (See id. ¶¶ 144-46.) 26 This action was originally filed in the Los Angeles Superior 27 Court on January 23, 2014. (See Notice of Removal, Docket No. 1, p. 28 5-6.) Defendants removed the action on February 28, 2014 on grounds 2 1 of CAFA jurisdiction and federal question jurisdiction. (Id.) 2 Plaintiffs have now filed this Motion, seeking remand of the action 3 to state court. (Docket No. 12.) 4 II. Legal Standard 5 A defendant may remove a case from state court to federal 6 court if the case could have originally been filed in federal 7 court. 28 U.S.C. § 1441(a); see also Snow v. Ford Motor Co., 561 8 F.2d 787, 789 (9th Cir. 1977). As the removing party, a defendant 9 bears the burden of proving federal jurisdiction. Duncan v. 10 Stuetzle, 76 F.3d 1480, 1485 (9th Cir. 1996); see also Matheson v. 11 Progressive Specialty Ins. Co., 319 F.3d 1089, 1090 (9th Cir. 12 2003). The removal statute is strictly construed against removal 13 jurisdiction, and federal jurisdiction must be rejected if any 14 doubt exists as to the propriety of removal. Gaus v. Miles, Inc., 15 980 F.2d 564, 566 (9th Cir. 1992) (explaining that courts resolve 16 doubts as to removability in favor of remand). 17 III. Discussion 18 A. CAFA Jurisdiction 19 Federal courts may exercise subject matter jurisdiction over a 20 “mass action” if it satisfies the jurisdictional requirements of 21 the Class Action Fairness Act (“CAFA”). 28 U.S.C. § 1332(d)(11). 22 One of the requirements for CAFA jurisdiction is that the action 23 must involve “monetary relief claims of 100 or more persons” that 24 are “proposed to be tried jointly on the ground that the 25 plaintiffs’ claims involve common questions of law or fact.” Id. 26 Defendants contend that they can meet the 100 plaintiff 27 requirement under CAFA by aggregating the claims of plaintiffs in 28 related cases filed by Plaintiffs’ counsel and the claims of 3 1 potential plaintiffs listed on a “Notice of Claims” filed in this 2 action. Further, Defendants argue that because Plaintiffs filed a 3 notice of related cases in this action and because Plaintiffs filed 4 a multidistrict litigation (“MDL”) motion in one of the related 5 cases (which did not purport to include the instant case), the 6 Court should find that Plaintiffs have implicitly tried to join 7 their claims. 8 The Ninth Circuit has held that “CAFA’s ‘mass action’ 9 provisions do not permit a defendant to remove to federal court 10 separate state court actions, each involving the monetary claims of 11 fewer than one hundred plaintiffs.” Tanoh v. Dow Chem. Co., 561 12 F.3d 945, 953 (9th Cir. 2009). As a result, Defendants’ argument 13 that the plaintiffs in the related cases should be aggregated with 14 Plaintiffs here is unavailing. In addition, Plaintiffs in this case 15 have not sought to have this action consolidated with other 16 actions, as this was not one of the cases before the MDL panel.1 17 Therefore, the claims in this case may not be aggregated with the 18 claims filed in the related actions in order to meet the CAFA 19 numerosity requirement. 20 Further, Defendants cite no authority for the proposition that 21 the CAFA numerosity requirement can be met by aggregating potential 22 plaintiffs who have not even filed a claim. See Carolyne v. 23 USPLabs, LLC, 2014 WL 1118017, at *3 (C.D. Cal. 2014) (finding no 24 CAFA jurisdiction in one of the cases related to this action). 25 There is no indication that any of these potential plaintiffs plans 26 to file a claim, and the Court will not speculate as to whether and 27 28 1 The MDL panel has denied the multidistrict litigation motion. 4 1 when these individuals may choose to file suit or whether, should 2 they choose to do so, their claims will be sufficiently similar to 3 the claims at issue in this action to warrant joining the cases for 4 trial.2 Therefore, the Court finds that Defendants have not met 5 their burden of showing that subject matter jurisdiction exists 6 under CAFA and that removal on this basis is thus improper. 7 B. Federal Question Jurisdiction 8 Federal question jurisdiction exists where a civil action 9 arises “under the Constitution, laws, or treaties of the United 10 States.” 28 U.S.C. § 1331. “For a case to ‘arise under’ federal 11 law, a plaintiff’s well-pleaded complaint must establish either (1) 12 that federal law creates the cause of action or (2) that the 13 plaintiff's asserted right to relief depends on the resolution of a 14 substantial question of federal law. Federal jurisdiction cannot 15 hinge upon defenses or counterclaims, whether actual or 16 anticipated.” K2 Am. Corp. v. Roland Oil & Gas, LLC, 653 F.3d 1024, 17 1029 (9th Cir. 2011). Where federal law does not create the cause 18 of action, “the question is, does a state-law claim necessarily 19 raise a stated federal issue, actually disputed and substantial, 20 which a federal forum may entertain without disturbing any 21 congressionally approved balance of federal and state judicial 22 responsibilities.” Grable & Sons Metal Products, Inc. v. Darue 23 Engineering & Mfg., 545 U.S. 308, 314 (2005). 24 25 2 26 27 28 Plaintiffs argue that even if the Court might consider such potential claims in evaluating whether CAFA jurisdiction is appropriate, many of the potential plaintiffs listed in their Notice of Claims have injuries resulting from ingestion of a different chemical (aegeline), which would raise different issues than are present in the current action regarding DMAA. 5 1 Plaintiffs bring purely state law claims in this action: 2 negligence, strict products liability for design defects and 3 failure to warn, breach of warranty, and UCL claims. Defendants 4 argue that this Court has federal question jurisdiction over this 5 action because “Plaintiffs’ Complaint attempts to assert claims 6 based on Defendants’ alleged failure to comply with federal laws, 7 regulations and directives regarding sales and distribution of 8 their Jack3d and OxyElite dietary supplement products.” (Opp. to 9 Mtn., Docket No. 17, p. 2.) This statement mischaracterizes 10 11 Plaintiffs’ claims. Although Plaintiffs mention the Food and Drug Administration’s 12 warning letters to Defendants regarding the products at issue, no 13 interpretation of federal law will be necessary to adjudicate the 14 state law claims. The interactions with the FDA, at most, are 15 evidence that Defendants knew or should have known of the 16 detrimental effects of DMAA and evidence that DMAA is actually 17 unsafe. Plaintiffs could succeed on all of the claims at issue in 18 this case without any reference to the FDA or to any federal law, 19 as a determination of whether the FDA has or has not approved, 20 disapproved, or outlawed DMAA is not necessarily dispositive of 21 whether Defendants in this case should have known about the dangers 22 their products pose and whether they should have warned consumers 23 of that danger. 24 Further, to the extent that a federal issue is actually raised 25 at all, “the mere presence of a federal issue in a state cause of 26 action does not automatically confer federal-question 27 jurisdiction.” Merrell Dow Pharms., Inc., v. Thompson, 478 U.S. 28 804, 813 (1986). Even if the presence of Plaintiffs’ allegations 6 1 regarding the FDA will require some interpretation of how the 2 federal regulatory scheme works in order to understand the import 3 of the FDA warnings, and even if this interpretation could be 4 construed as a “federal issue,” that issue is minor, not 5 “substantial.” See Nevada v. Bank of America Corp., 672 F.3d 661, 6 675 (9th Cir. 2012) (finding no federal jurisdiction where “the 7 federal issues ... [were] not ‘pivotal’ to [Plaintiff’s] case”). As 8 a result, the Court finds that Defendants have not met their burden 9 of demonstrating that the Court has federal subject matter 10 jurisdiction over this action. 11 IV. Conclusion 12 For the foregoing reasons, the Motion is GRANTED. The action 13 is remanded to the Los Angeles Superior Court. Defendants’ motion 14 to dismiss (Docket No. 10) is DENIED AS MOOT. 15 16 IT IS SO ORDERED. 17 18 19 Dated: April 25, 2014 DEAN D. PREGERSON United States District Judge 20 21 22 23 24 25 cc: order, docket, remand letter to Los Angeles Superior Court, No. BC 534065 26 27 28 7

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