Goico v. United States Food and Drug Administration

CourtDistrict Court, D. Kansas
DecidedJanuary 19, 2021
Docket6:20-cv-01248
StatusUnknown

This text of Goico v. United States Food and Drug Administration (Goico v. United States Food and Drug Administration) is published on Counsel Stack Legal Research, covering District Court, D. Kansas primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Goico v. United States Food and Drug Administration, (D. Kan. 2021).

Opinion

IN THE UNITED STATES DISTRICT COURT FOR THE DISTRICT OF KANSAS

PETER MARIO GOICO,

Plaintiff,

v. Case No. 20-1248-JAR-KGG

UNITED STATES FOOD AND DRUG ADMINISTRATION and STEPHEN M. HAHN, COMMISSIONER OF FOOD AND DRUGS,

Defendants.

MEMORANDUM AND ORDER This matter comes before the Court on Plaintiff Peter Mario Goico’s pro se Motion to Reconsider (Doc. 36), which asks the Court to reconsider its December 3, 2020 Memorandum and Order (“December 3 Order”) dismissing this action for lack of standing. The motion is fully briefed, and the Court is prepared to rule.1 For the reasons set forth below, Plaintiff’s motion is denied. Very briefly, Plaintiff filed this action against Defendants, the U.S. Food and Drug Administration and its Commissioner, Stephen M. Hahn (collectively, the “FDA”), alleging that the FDA was unlawfully withholding hydroxychloroquine (“HCQ”) for the prevention of the SARS-CoV-2 (“COVID-19”) virus. Plaintiff sought injunctive relief in the form of an order “enjoin[ing] the FDA from disallowing prophylaxis [sic] use of hydroxychloroquine and enjoin[ing] any medical authority from punishing any doctor who prescribes hydroxychloroquine

1 Plaintiff did not file a reply in support of his Motion to Reconsider, and the time for doing so has passed. Plaintiff’s reply deadline was January 11, 2021. See D. Kan. Rule 6.1(d) (requiring that a reply be filed and served within 14 days of service of the response). as a prophylaxis for COVID-19.”2 In its December 3 Order, the Court dismissed this action after finding that Plaintiff lacked standing to sue because he had suffered no injury traceable to the FDA and because his alleged injury would not be redressed by the injunctive relief he sought.3 Plaintiff now seeks reconsideration of the December 3 Order under D. Kan. Rule 7.3(b), which applies to non-dispositive orders and judgments.4 However, the December 3 Order is

dispositive rather than non-dispositive, and D. Kan. Rule 7.3(a) therefore applies. That rule provides that “[p]arties seeking reconsideration of dispositive orders or judgments must file a motion pursuant to Fed. R. Civ. P. 59(e) or 60.”5 Because Plaintiff proceeds pro se, the Court is mindful that it must construe his pleadings liberally and apply a less stringent standard than that which is applicable to attorneys.6 Therefore, because Plaintiff filed his motion to reconsider within twenty-eight days of the Court’s order, the Court construes Plaintiff’s motion as one seeking to alter or amend judgment under Fed. R. Civ. P. 59(e).7 Grounds which justify alteration or amendment under Rule 59(e) include: (1) an intervening change in controlling law; (2) new evidence that was previously unavailable; or (3) a need to correct clear error or prevent manifest injustice.8 A Rule 59(e) motion does not permit a

losing party to rehash arguments previously addressed or to present new legal theories or facts

2 Doc. 1 at 3. 3 Doc. 34 at 12−16. 4 D. Kan. Rule. 7.3(b)(2). 5 D. Kan. Rule 7.3(a). 6 Whitney v. New Mexico, 113 F.3d 1170, 1173 (10th Cir. 1997). 7 See Hayes Fam. Tr. v. State Farm Fire & Cas. Co., 845 F.3d 997, 1004 (10th Cir. 2017) (“No matter how styled, a motion will be deemed a Rule 59(e) motion if it is served within the specified time period and seeks relief appropriate to Rule 59(e) by questioning the correctness of the underlying judgment.”) (citing Hannon v. Maschner, 981 F.2d 1142, 1144 n.2 (10th Cir. 1992))); Fed. R. Civ. P. 59(e) (stating that “[a] motion to alter or amend a judgment must be filed no later than 28 days after the entry of the judgment”). 8 Hayes Fam. Tr., 845 F.3d at 1004 (citing Servants of the Paraclete v. Does, 204 F.3d 1005, 1012 (10th Cir. 2000)). that could have been raised earlier.9 A party’s failure to present its strongest case in the first instance does not entitle it to a second chance in the form of a motion to alter or amend.10 Whether to grant a motion to alter or amend is left to the Court’s discretion.11 Plaintiff’s motion to reconsider consists of two paragraphs in which he asserts that the Court should alter its ruling based on new evidence. Specifically, Plaintiff contends that the

American Medical Association (“AMA”) and the FDA have now “reversed themselves” on the prophylactic use of HCQ; that the only thing that has changed to bring about this reversal is politics, with the passing of the presidential election; and that the FDA’s change in opinion on the safety and effectiveness of HCQ for the treatment or prevention of COVID-19 is proof that the FDA was “being arbitrary and capricious” and lied to the Court.12 Plaintiff attaches as an exhibit to his motion an article entitled, “UPDATE: American Medical Association Considers Resolution on Statement Against Prescription of Hydroxychloroquine for COVID-19 Patients.”13 Nothing in Plaintiff’s motion or the attached exhibit warrants alteration or amendment of the December 3 Order. In that Order, the Court found that Plaintiff lacked standing because he

had failed to establish the required elements of causation and redressability. First, because the FDA was not actually withholding HCQ or preventing physicians from prescribing it, as Plaintiff claimed, he failed to allege a causal connection between his injury and the FDA’s conduct

9 Servants of the Paraclete, 204 F.3d at 1012; see also Steele v. Young, 11 F.3d 1518, 1520 n.1 (10th Cir. 1993). 10 Turner v. Nat’l Council of State Bds. of Nursing, Inc., No. 11-2059-KHV, 2013 WL 139750, at *2 (D. Kan. Jan. 10, 2013) (citing Cline v. S. Star Cent. Gas Pipeline, Inc., 370 F. Supp. 2d 1130, 1132 (D. Kan. 2005), aff'd, 191 F. App’x 822 (10th Cir. 2006)); Kestrel Holdings I, L.L.C. v. Learjet Inc., No. 02-2388-CM, 2006 WL 2575719, at *2 (D. Kan. Mar. 30, 2006). 11 Coffeyville Res. Refining & Mktg., LLC v. Liberty Surplus Ins. Corp., 748 F. Supp. 2d 1261, 1264 (D. Kan. 2010) (citing In re Motor Fuel Temp. Sales Pracs. Litig., 707 F. Supp. 2d 1145, 1166 (D. Kan. 2010)); Kestrel Holdings I, L.L.C., 2006 WL 2575719, at *2. 12 Doc. 36 at 1. 13 Id. at 2−6. sufficient to establish standing. As the Court explained, the independent decisions of third-party medical professionals not to prescribe HCQ are not fairly traceable to the FDA.14 Second, Plaintiff failed to satisfy the redressability element of standing because he could not show that it was likely, rather than speculative, that his injury would be redressed by a decision in his favor. Again, because the FDA was not prohibiting the use of HCQ, and it has no power over state

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Goico v. United States Food and Drug Administration, Counsel Stack Legal Research, https://law.counselstack.com/opinion/goico-v-united-states-food-and-drug-administration-ksd-2021.