Williamson v. Genentech, Inc.

CourtDistrict Court, N.D. California
DecidedMarch 18, 2020
Docket3:19-cv-01840
StatusUnknown

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

Bluebook
Williamson v. Genentech, Inc., (N.D. Cal. 2020).

Opinion

1 2 3 4 UNITED STATES DISTRICT COURT 5 NORTHERN DISTRICT OF CALIFORNIA 6 7 ANDREW WILLIAMSON, Case No. 19-cv-01840-JSC

8 Plaintiff, ORDER REMANDING ACTION TO 9 v. STATE COURT FOR LACK OF SUBJECT MATTER JURISDICTION 10 GENENTECH, INC., et al.,

Defendants. 11

12 13 Andrew Williamson brings this action on behalf of himself and other similarly situated 14 individuals alleging that Genentech Inc.’s sale of prescription drugs in single-dose vials results in 15 waste of medication and violates California’s Unfair Competition Law, California Business and 16 Professions Code § 17200 (the “UCL”). Genentech’s motion to dismiss the complaint based on 17 federal impossibility preemption, or alternatively, based on California’s judicial-abstention 18 doctrine or for failure to state a claim came before the Court for a hearing on November 21, 2019.1 19 (Dkt. No. 30.) At the hearing, the Court noted that before addressing Genentech’s motion, it must 20 ensure that it has Article III standing to hear this action which was removed from the Superior 21 Court for San Mateo County under the Class Action Fairness Act (“CAFA”), 28 U.S.C. § 1332(d). 22 (Dkt. No. 53.) The parties have since submitted supplemental briefing on this issue. (Dkt. Nos. 23 59, 62, 63.) Having considered the parties’ briefs and having had the benefit of oral argument on 24 November 21, 2019, the Court concludes that it lacks subject matter jurisdiction and REMANDS 25 the action to state court. 26 // 27 1 SECOND AMENDED COMPLAINT ALLEGATIONS 2 Genentech is a biotechnology company based in California. (Second Amended Complaint 3 (“SAC”), Dkt. No. 26 at ¶ 20.2) Among Genentech’s FDA-approved medications are four that are 4 at issue in this action: Avastin (for treatment of colorectal and other cancers), Rituxan (for 5 treatment of non-Hodgkin’s Lymphoma and other conditions), Kadeyla (for treatment of breast 6 cancer), and Xolair (for treatment of asthma). (Id. at ¶¶ 23-32.) These medications are all sold in 7 single use vials that are available in the United States in two sizes in the case of Avastin, Rituxan, 8 and Kadeyla, and one size in the case of Xolair. (Id. at ¶¶ 24, 27, 30, 33.) 9 In January of 2016, Plaintiff was treated with Rituxan for Follicular Lymphoma. (Id. at ¶ 10 97.) Over the next five months, he received six 772.5 mg doses of Rituxan. (Id. at ¶ 98.) On each 11 occasion, “the hospital used either eight 100 mg vials or one 500 mg vial and three 100 mg vials.” 12 (Id.) The total charge for this treatment was $34,189.33. (Id.) From September 2016 through 13 August 2017, Plaintiff was given a second course of treatment, receiving a single 780 mg dose 14 each time. (Id. at ¶ 99.) For this second round of treatment, the hospital used one 500 mg vial and 15 three 100 mg vials. (Id.) The charge for the first four administrations of this treatment was 16 $37,464.99 per treatment and the charge for the final treatment was $43,230.99. (Id.) In 17 November 2017 and in March 2018, Plaintiff had a third course of treatment where he received 18 doses of 800 mg using one 500 mg vial and three 100 mg vials for a total cost of $43,230.99. (Id. 19 at ¶ 100.) For all but the last two treatments, because he received a dose of less than 800 mg and 20 Rituxan was only sold in 100 mg or 500 mg vials, 20-27.5 mg of Rituxan were discarded as waste. 21 (Id. at ¶ 101.) For each of these treatments, some or all of the hospital charges were paid by 22 Plaintiff’s insurer; however, he paid $231.15 out-of-pocket for his March 2, 2017 treatment. (Id. 23 at ¶ 103.) 24 Based on these allegations, Plaintiff brings a single claim for violation of California’s 25 Unfair Competition Law. In particular, Plaintiff alleges as unfair “Genentech’s practices of selling 26 drugs in quantities that inherently lead to wasted amounts of medicine, causing substantial injury 27 1 to Plaintiff and the Class who are forced to purchase large amounts of medications that they do not 2 and cannot use.” (Dkt. No. 26 ¶ 167.) 3 LEGAL STANDARD 4 “Federal courts are courts of limited jurisdiction. They possess only that power authorized 5 by Constitution and statute.” Kokkonen v. Guardian Life Ins. Co. of Am., 511 U.S. 375, 377 6 (1994). “Only state-court actions that originally could have been filed in federal court may be 7 removed to federal court by the defendant.” Caterpillar Inc. v. Williams, 482 U.S. 386, 392 8 (1987). CAFA vests federal courts with original jurisdiction over class actions in which: (1) the 9 amount in controversy exceeds $5,000,000; (2) diversity of citizenship exists between at least one 10 plaintiff and one defendant; and (3) the number of plaintiffs in the class is at least one hundred. 28 11 U.S.C. § 1332(d)(2), (5), (6). “The rule that a removed case in which the plaintiff lacks Article III 12 standing must be remanded to state court under § 1447(c) applies as well to a case removed 13 pursuant to CAFA as to any other type of removed case.” Polo v. Innoventions Int’l, LLC, 833 14 F.3d 1193, 1196 (9th Cir. 2016); see also 28 U.S.C. § 1447(c) (“If at any time before final 15 judgment it appears that the district court lacks subject matter jurisdiction, the case shall be 16 remanded.”). 17 A defendant seeking removal to federal court “bears the burden of establishing that 18 removal is proper,” and the “removal statute is strictly construed against removal jurisdiction.” 19 Provincial Gov’t of Marinduque v. Placer Dome, Inc., 582 F.3d 1083, 1087 (9th Cir. 2009). “The 20 burden of establishing removal jurisdiction, even in CAFA cases, lies with the defendant seeking 21 removal.” Washington v. Chimei Innolux Corp., 659 F.3d 842, 847 (9th Cir. 2011). 22 DISCUSSION 23 “[C]ourts have an ‘independent obligation’ to police their own subject matter jurisdiction, 24 including the parties’ standing.” Animal Legal Def. Fund v. United States Dep’t of Agric., 935 25 F.3d 858, 866 (9th Cir. 2019) (citations omitted). To do so, the court must assure itself that 26 “Plaintiffs have alleged an injury in fact, fairly traceable to the defendant’s conduct, and likely to 27 be redressed by a favorable judicial decision.” Id. (citing Spokeo, Inc., v. Robins, ––– U.S. ––––, 1 suffered ‘an invasion of a legally protected interest’ that is ‘concrete and particularized’ and 2 ‘actual or imminent, not conjectural or hypothetical.’” Animal Legal Def. Fund, 935 F.3d at 866 3 (quoting Spokeo, 136 S. Ct. at 1548). “A ‘particularized’ injury is one that affects the plaintiff 4 personally, and a ‘concrete’ injury ‘must actually exist.’” Animal Legal Def. Fund, 935 F.3d at 5 866. 6 The Court raised two primary concerns regarding Article III standing: (1) whether 7 Plaintiff has plausibly alleged facts that support a finding that he has standing to pursue a claim 8 regarding any drug other than Rituxan as there is no allegation that he was ever prescribed or 9 administered Avastin, Kadcyla, or Xolair (the other drugs referenced in the Second Amended 10 Complaint) or is ever likely to be, and (2) whether Plaintiff has alleged facts that show a 11 particularized and concrete injury.

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Williamson v. Genentech, Inc., Counsel Stack Legal Research, https://law.counselstack.com/opinion/williamson-v-genentech-inc-cand-2020.