Andre-Rodney v. Hochul

CourtDistrict Court, N.D. New York
DecidedAugust 1, 2022
Docket1:21-cv-01053
StatusUnknown

This text of Andre-Rodney v. Hochul (Andre-Rodney v. Hochul) is published on Counsel Stack Legal Research, covering District Court, N.D. New York primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Andre-Rodney v. Hochul, (N.D.N.Y. 2022).

Opinion

UNITED STATES DISTRICT COURT NORTHERN DISTRICT OF NEW YORK

DAPHNE JANE ANDRE-RODNEY, JOHN LUDEWIG, ORIE MONROE, RYAN G. RICHARDS, RAYMOND SMITH, PAUL J. WILLIAMS, SYED AZAD, MICHAEL 1:21-cv-1053 (BKS/CFH) THOMAS FINELLI, and BRYAN REEVES,

Plaintiffs,

v.

KATHY HOCHUL, in her official capacity as Governor of New York State, NEW YORK STATE, MARY T. BASSETT, in her official capacity as Health Commissioner of New York State,1 NEW YORK STATE DEPARTMENT OF HEALTH, and NEW YORK STATE PUBLIC HEALTH AND PLANNING COUNCIL,2

Defendants.

Appearances: For Plaintiffs: Dennis C. Vacco Lippes Mathias LLP 50 Fountain Plaza, Suite 1700 Buffalo, NY 14202 For Defendants: Letitia James Attorney General of the State of New York Jorge A. Rodriguez Brittany M. Haner Assistant Attorneys General, of Counsel The Capitol Albany, NY 12224

1 Pursuant to Fed. R. Civ. P. 25(d), the current Commissioner of Health, Mary T. Bassett, has been substituted in place of her predecessor, Commissioner Howard Zucker. 2 It appears that the correct name of this entity is the Public Health and Health Planning Council. (Dkt. No. 1-1, at 2). Hon. Brenda K. Sannes, United States District Judge: MEMORANDUM-DECISION AND ORDER I. INTRODUCTION Plaintiffs Daphnee Jane Andre-Rodney and Michael T. Finelli,3 New York State Security Services Assistants who currently work at hospitals located in New York State, bring this action against Defendants under 42 U.S.C. § 1983 to challenge the mandate that they be “fully

vaccinated against COVID-19” as violative of their constitutional rights. (Dkt. No. 1); see 10 N.Y.C.R.R. § 2.61(c) (Aug. 26, 2021). On November 1, 2021, after briefing and a telephonic hearing, the Court denied Plaintiffs’ motion for a preliminary injunction, finding that Plaintiffs had not made a showing of a likelihood of success on the merits of their constitutional claims or of irreparable harm. See generally Andre-Rodney v. Hochul, 569 F. Supp. 3d 128 (N.D.N.Y. 2021). Presently before the Court is Defendants’ motion to dismiss Plaintiffs’ Complaint pursuant to Federal Rule of Civil Procedure 12(b)(6) for failure to state a claim. (Dkt. No. 21). Plaintiffs opposed the motion, (Dkt. No. 25), and Defendants responded, (Dkt. No. 28).4 For the following reasons, Defendants’ motion is granted.

3 Since commencement of this action, the seven other original plaintiffs have either retired or received the COVID-19 vaccine and returned to work. (Dkt. No. 21-2, at 4). Plaintiffs acknowledge that these seven plaintiffs “no longer have standing” in this action. (Dkt. No. 25, at 3 n.1). “A federal court loses jurisdiction to entertain a claim that has become moot.” Libertarian Party of Erie County v. Cuomo, 970 F.3d 106, 116 (2d Cir. 2020), abrogated on other grounds, New York State Rifle & Pistol Ass’n v. Bruen, 142 S. Ct. 2111 (2022). Therefore, the claims asserted by Plaintiffs Ludewig, Monroe, Richards, Smith, Williams, Azad, and Reeves are moot and must be dismissed for lack of subject matter jurisdiction. Chevron Corp. v. Donziger, 833 F.3d 74, 123–24 (2d Cir. 2016) (“A case is moot when ‘the parties lack a legally cognizable interest in the outcome.’” (citation omitted)). 4 Plaintiffs filed a letter requesting that the Court schedule oral argument on the motion to dismiss. (Dkt. No. 30). Such requests are “subject to the discretion of the presiding judge.” N.D.N.Y. L.R. 7.1(a). Having reviewed the parties’ thorough submissions, the Court finds oral argument unnecessary. II. FACTS5 A. COVID-19 Vaccines This case arises out of regulations adopted by the Public Health and Health Planning Council (the “Council”) of the New York State Department of Health (“DOH”) in response to the COVID-19 pandemic. The United States Department of Health and Human Services declared COVID-19 a public health emergency on February 4, 2020. (Dkt. No. 1, ¶ 28). Pharmaceutical

companies Pfizer, Moderna, and Johnson & Johnson (“Janssen”) all applied for and received emergency use authorization (“EUA”) for the COVID-19 vaccines each developed. (Id. ¶ 31). On August 23, 2021, the Food and Drug Administration (“FDA”) fully approved the Pfizer vaccine for individuals 16 years of age and older. (Id. ¶ 32).6 The Moderna and Janssen vaccines retain their EUA but have not yet been fully approved by the FDA, meaning they “have not gone through the typical six stages of approval.” (Id. ¶ 33). Plaintiffs allege that, although the COVID-19 vaccines “appear to be relatively safe at a population level, like all medical interventions, the vaccines carry a risk of side effects.” (Id. ¶ 34). Such side effects “include common, temporary reactions such as pain and swelling at the

vaccination site, fatigue, headache, muscle pain, fever, and nausea.” (Id.). “More rarely,” the vaccines can cause “serious side effects that could result in hospitalization or death.” (Id.). Research “indicates that the vaccines present a heightened risk of adverse side effects to those

5 The facts are drawn from the Complaint and the exhibits attached thereto. The Court assumes the truth of, and draws reasonable inferences from, the well-pleaded factual allegations. Faber v. Metro. Life Ins. Co., 648 F.3d 98, 104 (2d Cir. 2011). 6 The Court notes that, since commencement of this action, the FDA authorized the Moderna vaccine for use in adults 18 years of age and older, and the Pfizer and Moderna vaccines have received EUA for individuals as young as six months old. See “Coronavirus (COVID-19) Update: FDA Authorizes Moderna and Pfizer-BioNTech COVID-19 Vaccines for Children Down to 6 Months of Age,” (June 17, 2022), https://www.fda.gov/news-events/press- announcements/coronavirus-covid-19-update-fda-authorizes-moderna-and-pfizer-biontech-covid-19-vaccines- children; see Basank v. Decker, 449 F. Supp. 3d 205, 211–12 (S.D.N.Y. 2020) (taking judicial notice of background information regarding COVID-19 taken from the website of the Centers for Disease Control and Prevention (“CDC”)). who have previously contracted and recovered from COVID-19.” (Id. ¶ 35). Between December 14, 2020 and September 7, 2021, the CDC’s Vaccine Adverse Event Reporting System received 7,439 reports of death “among people that have received a COVID-19 vaccination.” (Id. ¶ 36). Plaintiffs allege that “the long-term effects” of the COVID-19 vaccines “remain unknown and

unstudied.” (Id. ¶ 37). B. The Vaccine Mandate DOH has the authority to “supervise and regulate the sanitary aspects” of “businesses and activities affecting public health.” N.Y. Pub. Health Law § 201(1)(m). Pursuant to its authority, DOH published a proposed emergency regulation for review and adoption by the Council. (See Dkt. No. 1-1, at 9). The Council adopted the emergency regulation on August 26, 2021; the regulation immediately went into effect for ninety days. (See Dkt. No. 1, ¶ 42; see also Dkt. No. 1-1 (text of the adopted amended regulation and its Regulatory Impact Statement)); see 10 N.Y.C.R.R. § 2.61 (Aug. 26, 2021) (regulation as codified) (the “Vaccine Mandate”). The Vaccine Mandate was adopted against the backdrop of the predominance of the Delta variant of the COVID-19 virus, a variant which was more transmissible than previous variants. (Dkt. No. 1-

1, at 11).

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