Asbestos Disease Awareness Organization v. Wheeler

CourtDistrict Court, N.D. California
DecidedNovember 15, 2019
Docket3:19-cv-00871
StatusUnknown

This text of Asbestos Disease Awareness Organization v. Wheeler (Asbestos Disease Awareness Organization v. Wheeler) 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
Asbestos Disease Awareness Organization v. Wheeler, (N.D. Cal. 2019).

Opinion

1 2 3 4 UNITED STATES DISTRICT COURT 5 NORTHERN DISTRICT OF CALIFORNIA 6 7 ASBESTOS DISEASE AWARENESS Case No. 19-cv-00871-EMC ORGANIZATION, et al., 8 Plaintiffs, ORDER DENYING DEFENDANT’S 9 MOTION TO DISMISS v. 10 Docket No. 16 ANDREW WHEELER, et al., 11 Defendants. 12 13 14 Plaintiffs1 are a group of nonprofit public health and environmental organizations that 15 promote awareness of the risks associated with asbestos in our environment. This suit against the 16 Environmental Protection Agency (“EPA”) and its Acting Administrator, Andrew Wheeler, 17 challenges the EPA’s denial of their petition to initiate rulemaking. Docket No. 1. This action is 18 brought under the Toxic Substance Control Act (“TSCA”) which provides under some 19 circumstances de novo review of the EPA decision. The suit also asserts a claim under the 20 Administrative Procedure Act (“APA”). Pending before the Court is the EPA’s motion to dismiss 21 the FAC’s APA claim for lack of subject matter jurisdiction. The EPA’s motion initially did not 22 challenge Plaintiffs’ TSCA claim, although the scope of the claim is now at issue. 23 I. BACKGROUND 24 A. Statutory Background 25 Congress enacted the TSCA in 1976 to create a national program for assessing and 26 1 Asbestos Disease Awareness Organization (“ADAO”), American Public Health Association 27 (“APHA”), Center for Environmental Health (“CEH”), Environmental Working Group (“EWG”), 1 managing the risks of chemicals to human health and the environment. Section 2(b)2 of the TSCA 2 requires the following from the EPA: (1) “adequate information should be developed with respect 3 to the effect of chemical substances and mixtures on health and the environment” and (2) 4 “adequate authority should exist to regulate chemical substances and mixtures which present an 5 unreasonable risk of injury to health or the environment.” 15 U.S.C. § 2601(b)(1)–(2). However, 6 “authority over chemical substances and mixtures should be exercised in such a manner as not to 7 impede unduly or create unnecessary economic barriers to technological innovation while 8 fulfilling the primary purpose of this chapter to assure that such innovation and commerce in such 9 chemical substances and mixtures do not present an unreasonable risk of injury to health or the 10 environment.” Id. at § 2601(b)(3). 11 Section 6(a) provides the EPA with authority to regulate substances that present “an 12 unreasonable risk of injury” to human health or the environment. 15 U.S.C. § 2605(a). Section 13 6(a) also lists examples of chemical lifecycle phases (e.g., manufacturing, processing, usage, and 14 disposal, etc.) which the EPA is authorized to regulate. Id. Moreover, Section 6(a) provides that 15 “[i]f the [EPA] Administrator determines . . . that the . . . use . . . of a chemical substance presents 16 an unreasonable risk of injury to health or the environment, the Administrator shall by rule” 17 impose one or more authorized restrictions, which include limiting or banning the manufacture or 18 distribution of the chemical for a particular use. Id. 19 Section 8(a)(1) provides that the EPA “shall promulgate rules” that require each person 20 who manufactures or processes a chemical substance to submit a report as the “Administrator may 21 reasonably require.” 15 U.S.C. § 2607(a). The EPA is prohibited, however, by Section 8(a)(5)(A) 22 from requiring reporting that is “unnecessary or duplicative” and must apply the reporting 23 obligations under Section 8(a) only to those persons who are likely to have the relevant 24 information. Id. at § 2607(a)(5)(A)–(C). In 2011, pursuant to its authority under Section 8(a)(1), 25 the EPA promulgated the Chemical Data Reporting (“CDR”) rule that required reporting for all 26 27 1 chemicals3 manufactured or imported at a site in the amount of 25,000 pounds or more in a given 2 reporting year from 2012 onward. See 40 C.F.R. § 711.8(a)(1). 3 On June 22, 2016, Congress amended the TSCA with the Frank R. Lautenberg Chemical 4 Safety for the 21st Century Act (“LCSA”). The amendment established a new integrated process 5 under Section 6:

6 The Administrator shall designate as a high-priority substance a chemical substance that the Administrator concludes . . . may 7 present an unreasonable risk of injury to health or the environment because of a potential hazard and a potential route of exposure under 8 the conditions of use, including an unreasonable risk to a potentially exposed or susceptible subpopulation identified as relevant by the 9 Administrator. 10 15 U.S.C. § 2605(b)(1)(B)(i). 11 Section 6(b)(2)(A) required the EPA to initiate risk evaluations on ten chemical substances 12 within six months after the enactment of the LCSA. The EPA designated asbestos as one of the 13 ten chemicals to undergo risk evaluation. See 81 Federal Register 91927 (“As amended, the law 14 requires that risk evaluation be initiated on 10 chemical substances drawn from the 2014 update of the 15 TSCA Work Plan for Chemical Assessments”). According to the EPA, that evaluation is ongoing. 16 After 2016, “any chemical substance that is the subject of a rule proposed or promulgated under 17 TSCA [Section 6]” is subject to a 2,500-pound volume threshold for reporting. 40 C.F.R. § 18 711.8(b). 19 Section 21 contains a citizen-petition process under which the public can seek to compel 20 the EPA to engage in its rulemaking authority. 15 U.S.C. § 2620(a). If unsuccessful at the agency 21 level, Section 21 enables the petitioner to file a civil action in federal district court for review of 22 the EPA’s determination. The standard of review at the district court is dependent on the relief 23 sought in the Petition. 24 For petitions seeking the issuance of a new rule, Section 21(b)(4)(A) provides, “[i]f the 25 Administrator denies a petition filed under this section . . . [,] the petitioner may commence a civil 26

27 3 Chemical substances for which information must be reported are described as “[a]ny chemical 1 action in a district court of the United States to compel the Administrator to initiate a rulemaking 2 proceeding as requested in the petition.” 15 U.S.C. § 2620(b)(4)(A). The standard of review for 3 new-rule petitions is further prescribed by Section 21(b)(4)(B), which provides, “[i]n an action 4 under subparagraph (A) respecting a petition to initiate a proceeding to issue a rule [], the 5 petitioner shall be provided an opportunity to have such petition considered by the court in a de 6 novo proceeding.” (emphasis added). 7 Section 21 does not offer guidance as to the standard of review for petitions seeking the 8 amendment or repeal of existing rules. However, case law analyzing Section 21’s legislative 9 history in this regard is instructive. In Environmental Defense Fund v. Reilly, the plaintiffs 10 petitioned the EPA under Section 21 to promulgate rules to prevent the release of dioxins and 11 furans into the environment. 909 F.2d 1497, 1449 (D.C. Cir. 1990). Specifically, they sought 12 record-keeping and reporting requirements so they could monitor results.

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