Doe v. Rumsfeld

501 F. Supp. 2d 186, 2007 U.S. Dist. LEXIS 60943, 2007 WL 2372391
CourtDistrict Court, District of Columbia
DecidedAugust 21, 2007
DocketCivil Action 03-707 (EGS)
StatusPublished
Cited by18 cases

This text of 501 F. Supp. 2d 186 (Doe v. Rumsfeld) is published on Counsel Stack Legal Research, covering District Court, District of Columbia primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Doe v. Rumsfeld, 501 F. Supp. 2d 186, 2007 U.S. Dist. LEXIS 60943, 2007 WL 2372391 (D.D.C. 2007).

Opinion

MEMORANDUM OPINION

SULLIVAN, District Judge.

Six plaintiffs, known as John Doe # 1 through # 4 and Jane Doe # 1 and # 2, brought this action to challenge the lawfulness of the defendants’ Anthrax Vaccination Immunization Program (“AVIP”). Currently pending before the Court is plaintiffs’ motion for attorneys’ fees and costs. Upon consideration of the motion, the response and reply thereto, the applicable law, and the entire record, the Court determines that plaintiffs are entitled to attorneys’ fees, but that their pending request is flawed in several, significant aspects. Therefore, for the reasons stated herein, plaintiffs’ motion for attorneys’ fees and costs is DENIED without prejudice.

BACKGROUND

This Court set forth a detailed description of the case’s regulatory and procedural background in its 2004 opinion, see Doe v. Rumsfeld, 341 F.Supp.2d 1, 3-8 (D.D.C. 2004), so it need only be summarized here. Pursuant to a process established for drugs whose regulation was transferred from the National Institutes of Health to the FDA, the FDA issued a proposed order concerning AVA in 1985. Id. at 4-6. The FDA panel, whose report was incorporated into the proposed order, concluded that AVA was safe and effective “under the limited circumstances for which it is employed.” Id. at 4-5. The panel did so after examining the “Brachman study,” which investigated AVA’s effectiveness against cutaneous anthrax and inhalation anthrax. Id. at 5. The proposed order recommended that AVA be placed in “Category I,” which encompassed drugs that are safe, effective, and not misbranded. Id. Pursuant to its regulations, the FDA published notice of the proposed rule and solicited comments for 90 days. Id. at 5-6. Following the receipt of comments, the *188 FDA took no further action until this suit was filed. Id. at 6.

In March 2003, plaintiffs filed suit in this Court, alleging that the AVIP violated federal law because AVA had never been approved as a safe and effective drug for protection against inhalation anthrax. Id. On December 22, 2003, the Court issued a preliminary injunction enjoining AVIP inoculations absent consent because the FDA had never issued a final decision regarding the safety of AVA. Id. Eight days later, the FDA issued a final order classifying AVA as a Category I drug, stating that it was effective regardless of the route of exposure. Id. The final order re-analyzed the data underlying the 1985 proposed order and also relied upon studies conducted after 1985. Id. at 7. Both parties subsequently moved for summary judgment, with plaintiff seeking permanent injunctive relief. Id. at 8.

On two initial matters, the Court determined the plaintiffs had standing and that the FDA’s December 2003 decision constituted an order, instead of a rule. Id. at 9-12. Even though the decision was an order, the Court concluded that because the FDA regulations required notice and comment for the order, the notice and comment must have been procedurally sufficient under the standards of the Administrative Procedure Act. Id. at 13. Utilizing the logical outgrowth doctrine, the Court concluded that the notice and comment for AVA was insufficient because the final order deviated too greatly from the proposed order. Id. at 15. Defendants had contended that the proposed order was substantively identical to the final order because the proposed order classified AVA as a Category I drug and did not limit its application to any particular route of exposure. Id. at 14. The Court, however, found that the scope of the proposed order’s recommendation did not include inhalation anthrax because the proposed order stated that there was insufficient data concerning AVA’s effectiveness against inhalation anthrax. Id. at 15. Therefore, the public was not on notice that AVA was being considered for use against inhalation anthrax specifically, and thus the FDA’s procedure did not provide a meaningful opportunity for comment as required by the FDA’s own regulations. Id. As a remedy, the Court vacated the final order and remanded it to the FDA for reconsideration. Id. at 16. In addition, the Court entered a permanent injunction enjoining defendants’ use of AVA absent consent until the FDA properly classified AVA as safe and effective for its intended purpose. Id. at 19.

While this case was on appeal, in December 2005, the FDA issued a new final order after a notice-and-comment period, explicitly finding AVA efficacious against inhalation anthrax. See Biological Products; Bacterial Vaccines and Toxoids; Implementation of Efficacy Review; Anthrax Vaccine Adsorbed, 70 Fed.Reg. 75,-180 (Dec. 19, 2005). As a result, the D.C. Circuit held that this Court’s permanent injunction had dissolved by its own terms, dismissed the appeal as moot, and remanded the case to this Court for further proceedings. Doe v. Rumsfeld, 172 Fed.Appx. 327 (D.C.Cir.2006) (per curiam). On remand, the only remaining issue is plaintiffs’ motion for attorneys’ fees and costs under the Equal Access to Justice Act (“EAJA”), 28 U.S.C. § 2412(d).

ANALYSIS

Plaintiffs have filed an application for $508,310.44 in attorneys’ fees and costs. Defendants first contend that plaintiffs are not entitled to any fees and costs because defendants’ position was substantially justified. In the alternative, defendants contend that the proper award is much less than plaintiffs’ request because (1) plain *189 tiffs are not prevailing parties with regard to their appeal to the D.C. Circuit; (2) plaintiffs’ requested rate for their counsel is above the statutory limit; and (3) plaintiffs’ purported billable hours are too high because they improperly seek reimbursement for certain activities and their billing records are too vague.

I. Substantial Justification

The EAJA provides that a prevailing party in a non-tort suit against the United States is entitled to fees and expenses unless the government’s position was “substantially justified.” 28 U.S.C. § 2412(d)(1)(A). The Supreme Court has held that a position is substantially justified “if a reasonable person could think it correct, that is, if it has a reasonable basis in law and fact.” Pierce v. Underwood, 487 U.S. 552, 556, 108 S.Ct. 2541, 101 L.Ed.2d 490 (1988). The D.C. Circuit has stated that “the hallmark of the substantial justification test is reasonableness.” Role Models Am., Inc. v. Brownlee, 353 F.3d 962, 967 (D.C.Cir.2004). The government bears the burden of establishing that its position was substantially justified. F.J. Vollmer Co., Inc. v. Magaw, 102 F.3d 591, 595 (D.C.Cir.1996).

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Bluebook (online)
501 F. Supp. 2d 186, 2007 U.S. Dist. LEXIS 60943, 2007 WL 2372391, Counsel Stack Legal Research, https://law.counselstack.com/opinion/doe-v-rumsfeld-dcd-2007.