Church v. Biden

CourtDistrict Court, District of Columbia
DecidedNovember 8, 2021
DocketCivil Action No. 2021-2815
StatusPublished

This text of Church v. Biden (Church v. Biden) 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
Church v. Biden, (D.D.C. 2021).

Opinion

UNITED STATES DISTRICT COURT FOR THE DISTRICT OF COLUMBIA

STEVEN CHURCH, et al., Plaintiffs, v. Civil Action No. 21-2815 (CKK) JOSEPH R. BIDEN, in his official capacity as President of the United States, et al., Defendants.

MEMORANDUM OPINION (November 8, 2021)

The plaintiffs in this case include eighteen federal civilian employees 1 and two active-duty

Marines 2 (collectively, “Plaintiffs”). By virtue of their federal civilian and military employment,

Plaintiffs are subject to the recent COVID-19 vaccine mandates imposed under President Joseph

R. Biden’s Executive Order 14043 and Secretary of Defense Lloyd Austin’s August 24, 2021 order

for the vaccination of military personnel. Plaintiffs now challenge these vaccine mandates on

constitutional and statutory grounds and request emergency injunctive relief preventing their

enforcement.

Plaintiffs’ “extraordinary” request for immediate injunctive relief is not merited. At this

early stage of the proceedings, the record reflects that each Plaintiff has requested an exemption

to the very COVID-19 vaccine mandates they challenge. These exemption requests all remain

pending, and during their pendency, no Plaintiff faces disciplinary action for refusing the

COVID-19 vaccine. Plaintiffs, therefore, come before this Court complaining of a compulsory

inoculation they may never need to take, and of adverse employment actions they may never

1 The “Federal Employee Plaintiffs” are: Steven Church, Lesley Church, Alma Gonzalez, Dynika Barnwell, Douglas Czerwinski, Jason Coffey, Joshua Schmidt, Melina Royer, Tamika Walls, Jaime Espitia, Somer Stephens, Alex Berne, Alan Camp, Stephanie Perrotta, Christopher Axtell, Grace Brown, Kristofor Hallfrisch, and Dorothy Morgan. 2 The “Service Member Plaintiffs” are: First Lieutenant Andrew Soto and Corporal Christopher Hall.

1 experience. This uncertainty weighs decisively against the ripeness of Plaintiffs’ claims and the

irreparability of their purported injuries. Emergency injunctive relief is not appropriate under these

circumstances. Accordingly, upon consideration of the pleadings, the relevant legal authorities,

and the record as a whole, 3 the Court DENIES Plaintiffs’ [5] Emergency Application for a

Temporary Restraining Order and Motion for Preliminary Injunction.

I. BACKGROUND

A. COVID-19 Pandemic & Vaccine Development

Coronavirus disease (“COVID-19”) is an infectious disease caused by the SARS-CoV-2

virus. 4 Spread principally by “exposure to respiratory fluids,” the “initial presentation of a

[COVID-19] infection ranges from no symptoms at all (asymptomatic) to severe illness and death;

and even after recovery, various long-term health problems may linger.” Klaasen v. Trustees of

Ind. Univ., --- F. Supp. 3d ---, 2021 WL 3073926, at *2 (N.D. Ind. July 18, 2021) (internal citations

omitted); see Defs.’ Opp’n Ex. 9, Decl. of Colonel Tonya Rans (“Rans Decl.”) ¶ 7, ECF No. 13-9. 5

Because the virus causing COVID-19 can “be easily transmitted to others prior to symptom

3 This Memorandum Opinion focuses on the following documents: x Verified Complaint for Declaratory and Injunctive Relief (“Compl.”), ECF No. 1; x Plaintiffs’ Memorandum of Law in Support of Plaintiffs’ Emergency Application for Temporary Restraining Order and Preliminary Injunction (“Pls.’ Mot.”), ECF No. 5-1; x Defendants’ Opposition to Emergency Application for Temporary Restraining Order and Preliminary Injunction (“Defs.’ Opp’n”), ECF No. 13; and x Plaintiffs’ Memorandum of Law in Reply to Defendants’ Opposition to Plaintiffs’ Application for Temporary Restraining Order and Preliminary Injunction (“Pls.’ Reply”), ECF No. 14. In an exercise of its discretion, the Court finds that holding oral argument in this action would not be of assistance in rendering a decision. See LCvR 7(f). 4 World Health Org., Coronavirus disease (COVID-19), https://www.who.int/health-topics/ coronavirus#tab=tab_1 (last visited Nov. 8, 2021). 5 See also CDC, Scientific Brief: SARS-CoV2 Transmission, https://www.cdc.gov/coronavirus/2019- ncov/science/science-briefs/sars-cov-2-transmission.html (last visited Nov. 8, 2021); CDC, People with Certain Medical Conditions, https://www.cdc.gov/coronavirus/2019-ncov/need-extra-precautions/people- with-medical-conditions.html (last visited Nov. 8, 2021); Neal M. Dixit et al., Post-Acute COVID-19 Syndrome and the Cardiovascular System: What is Known?, 5 Am. Heart. J. Plus. 100025 (May 2021), https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8223036/.

2 development,” it can “infect significant numbers before being identified.” Rans Decl. ¶ 9. In

recent months, a mutation of the SARS-CoV-2 virus known as the “Delta” variant has become the

dominant strain of the virus; it is twice as contagious as previous variants. Id. ¶ 5. 6 To date,

approximately 46 million cases of COVID-19 have been reported in the United States; the disease

has claimed the lives of more than 751,000 Americans. 7

As another federal district court summarized, “COVID-19 caught the world unaware.

Initially, there were no vaccines or treatments[.]” Klaassen, 2021 WL 3073926, at *8. Shortly

after then-President Donald J. Trump declared a national emergency on March 13, 2020, see 85

Fed. Reg. 15,337 (Mar. 13, 2020), the Secretary of the U.S. Department of Health and Human

Services (“HHS”) determined that “circumstances exist justifying the authorization of emergency

use of drugs and biological products during the COVID-19 pandemic,” see 85 Fed. Reg. 18,250,

18,250–51 (Apr. 1, 2020). In such circumstances, the U.S. Food and Drug Administration

(“FDA”) may issue an “emergency use authorization” (“EUA”) for FDA-regulated products

“intended for use” in responding to the emergency, before such products receive FDA “approval.”

See 21 U.S.C. § 360bbb-3(a)(1). In October 2020, the FDA issued guidance to vaccine developers,

“outlining [the FDA’s] expectations for vaccine sponsors,” including the “scientific data and

information” that would be required to obtain an EUA. 8

6 See also CDC, What We Know About the Science (Aug. 26, 2021), https://www.cdc.gov/coronavirus/ 2019-ncov/variants/delta-variant.html. 7 See CDC, COVID-19 Data Tracker, https://covid.cdc.gov/covid-data-tracker/#cases_casesper 100klast7days (last visited Nov. 8, 2021). 8 See FDA, Coronavirus (COVID-19) CBER-Regulated Biologics, Emergency Use Authorization, https://www.fda.gov/vaccines-blood-biologics/industry-biologics/coronavirus-covid-19-cber-regulated- biologics (last visited Nov. 8, 2021). The latest version of the FDA’s Industry Guidance was issued on May 25, 2021, superseding the original guidance issued in October 2020 and a second iteration dated February 22, 2021. See Emergency Use Authorization for Vaccines to Prevent COVID-19, Guidance for Industry (May 25, 2021), https://www.fda.gov/media/142749/download.

3 In late 2020 and early 2021, the FDA issued EUAs for COVID-19 vaccines developed by

three companies—Pfizer BioNTech, Moderna, and Johnson & Johnson.9 On August 23, 2021, the

FDA approved the vaccine created by Pfizer BioNTech, which would be marketed as “Comirnaty,”

for “the prevention of COVID-19 disease in individuals 16 years of age and older.” 10

B. Vaccine Mandates

1. Federal Employee Vaccine Mandate

On September 9, 2021, President Joseph R. Biden issued Executive Order 14043,

Requiring Coronavirus Disease 2019 Vaccination for Federal Employees. See Exec. Order 14043,

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