Geertson Farms, Inc. v. Johanns

439 F. Supp. 2d 1012, 2006 U.S. Dist. LEXIS 53931, 2006 WL 2085977
CourtDistrict Court, N.D. California
DecidedJuly 26, 2006
DocketC 06-01075 CRB
StatusPublished

This text of 439 F. Supp. 2d 1012 (Geertson Farms, Inc. v. Johanns) 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
Geertson Farms, Inc. v. Johanns, 439 F. Supp. 2d 1012, 2006 U.S. Dist. LEXIS 53931, 2006 WL 2085977 (N.D. Cal. 2006).

Opinion

MEMORANDUM AND ORDER

BREYER, District Judge.

Nine plaintiffs, comprised of organic farms and member organizations opposed to the over-use of pesticides and the propagation of genetically modified foods, are suing several government officials and agencies over the deregulation of alfalfa hay engineered to be genetically resistant to the common herbicide Roundup. In the Fourth Claim of the Complaint, Center for Food Safety (“CFS”), Beyond Pesticides, and Sierra Club (collectively referred to as “Plaintiffs”) claim the Environmental Protection Agency (“EPA”) violated the Endangered Species Act (“ESA”) when it determined the tolerance level of glyphosate in food for human consumption without consulting the Fish and Wildlife Service (“FWS”) to ascertain any potential effect on three endangered species.

Now pending before the Court is the EPA’s motion to dismiss this claim, the only claim against it, on the ground that the Court lacks subject matter jurisdiction pursuant to Rule 12(b)(1) of the Federal Rules of Civil Procedure. Defendants contend the suit is not properly brought in the federal district court for two reasons: 1) that plaintiffs failed to exhaust their administrative remedies available under the Federal Food Drug and Cosmetic Act (“FFDCA”), which grants exclusive jurisdiction over objections to tolerance levels to the EPA, and 2) plaintiffs lack standing to bring their claim. After carefully con *1014 sidering the parties’ memoranda, and with the benefit of oral argument, defendant’s motion is hereby GRANTED.

BACKGROUND

I. Factual Background

In 1999, Monsanto Company officially licensed Roundup Ready alfalfa, a species of alfalfa genetically engineered to be resistant to glyphosate, the main ingredient in its pesticide Roundup. Compl. ¶ 89. Alfalfa is the fourth most widely-grown crop in the United States after corn, soybeans, and wheat. Compl. ¶ 74. Alfalfa is consumed as hay and as seed; hay is a main source of nutrition for dairy and meat cows, chickens, sheep, and horses, and alfalfa seed has a variety of uses including direct human consumption in the form of alfalfa sprouts. Compl. ¶¶ 77, 79. Glyphosate is a common pesticide that blocks an enzyme essential for green plant growth.

Subsequent to licensing Roundup Ready Alfalfa, Monsanto filed a petition with the EPA requesting a tolerance level determination for glyphosate. On September 27, 2002, the EPA, pursuant to the FFDCA, established a tolerance of 400 ppm of gly-phosate in alfalfa hay. 67 Fed.Reg. 60934 (September 27, 2002.) On February 16, 2005, the EPA established a tolerance of 0.5 ppm for residues of glyphosate in alfalfa seed. Compl. ¶ 103.

In November 2004, Monsanto petitioned the USDA to deregulate genetically engineered alfalfa. In a Deregulation Determination published on June 27, 2005, the USDA concluded that the alfalfa engineered by Monsanto “would not present risk of plant pest introduction or dissemination,” 70 Fed.Reg. 36917, 36918, (June 27, 2005) and' that it “will not harm threatened or endangered species or organisms that are beneficial to agriculture; and... should not reduce the ability to control pests and weeds in alfalfa or other crops.” 70 Fed.Reg. at 36919 (June 27, 2005.) As a result, genetically engineered alfalfa would no longer be subject to the regulations established by the Department of Agriculture’s Animal and Plant Health Inspection Service (“APHIS”). Compl. ¶110.

The instant action brings six claims relating to two government agency actions: 1) the USDA’s deregulation of genetically engineered alfalfa, and 2) the EPA’s establishment of tolerance levels for the pesticide designed to be used on that alfalfa. The Fourth Claim, brought by three of the nine plaintiffs, addresses the second issue. The plaintiffs exhausted their administrative remedies under the ESA by giving the EPA sixty-days notice of the suit on November 18, 2005. Pis.’ Opp. at 12. The EPA filed this motion to dismiss on April 24, 2006, seeking to dismiss this claim for lack of subject matter jurisdiction based on plaintiffs’ failure to exhaust the exclusive administrative remedies of the FFDCA and on their lack of standing to bring the claim.

II. Relevant Statutes

A. FFDCA

The EPA regulates pesticides under two statutory schemes: the FFDCA and the Federal Insecticide, Fungicide, and Rodenticide Act (“FIFRA”). While both statutes examine health risks associated with pesticides, the FFDCA regulates the amount of pesticide that may safely be consumed in foods, while FIFRA governs the use, sale, and labeling of the pesticides themselves. Washington Toxics Coal. v. EPA, 413 F.3d 1024, 1030 (9th Cir.2005).

The FFDCA establishes the tolerance levels of pesticides in specific foods. These are the maximum levels of pesticide *1015 permitted for a food to be considered safe for human consumption and salable on the market. The act requires investigation into the best data available as to the “nature of any toxic effect shown to be caused by the pesticide chemical” on consumers. 21 U.S.C. § 346a(b)(2)(D). An EPA administrator may issue regulations “establishing, modifying, or revoking a tolerance for a pesticide chemical residue” on its own initiative or pursuant to a petition by an outside party. Id. § 346a(b)(l)(A), (B). If, as here, an outside party petitions to establish, modify, or revoke a tolerance level, the EPA may: (i) “issue a final regulation ... establishing, modifying, or revoking a tolerance [level];” (ii) issue a proposed regulation subject to public comment, “and thereafter issue a final regulation...;” or (iii) “issue an order denying the petition.” Id. § 346a(d)(4)(A).

The FFDCA further sets forth an administrative appeal process through which any person may object to the EPA’s decision regarding tolerance levels pursuant to section 346a(d)(4). Under that process, any person may file an objection within 60 days and request a public evidentiary hearing. 21 U.S.C. § 346a(g)(2)(A). The EPA must respond to an objection with a final order explaining its decision to modify or affirm its initial order. Id. § 346a(g)(2)(C). The FFDCA then permits “any person who will be adversely affected by such order or regulation” to obtain judicial review in the United States Court of Appeals.” Id. § 346a(h)(l). In 1996, the Food Quality Protection Act (“FQPA”) amended the FFDCA, adding the following language to subsection (h): “any issue as to which review is or was obtainable under this subsection shall not be the subject of judicial review under any other provision of law.” Id. § 346a(h)(5).

The FFDCA’s implementing regulations further explain that judicial review is not available for “[a]gency actions subject to the objection procedure of the FFDCA section [346a(g)(2) ] ...

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439 F. Supp. 2d 1012, 2006 U.S. Dist. LEXIS 53931, 2006 WL 2085977, Counsel Stack Legal Research, https://law.counselstack.com/opinion/geertson-farms-inc-v-johanns-cand-2006.