Jeremiah Hogan v. Lincoln Medical Partners

CourtListener 10376259Me04.03.2025

Gesamter Gesetzestext

MAINE SUPREME JUDICIAL COURT Reporter of Decisions
Decision: 2025 ME 22
Docket: Lin-24-209
Argued: November 12, 2024
Decided: March 4, 2025

Panel: STANFILL, C.J., and MEAD, HORTON, CONNORS, LAWRENCE, and DOUGLAS, JJ.

JEREMIAH HOGAN et al.

v.

LINCOLN MEDICAL PARTNERS et al.

HORTON, J.

[¶1] Jeremiah Hogan, Siara Jean Harrington, and their child (collectively,

Hogan) appeal from a judgment of the Superior Court (Lincoln County,

Billings, J.) dismissing—based on federal statutory immunity—a notice of claim

alleging that Lincoln Medical Partners; MaineHealth, Inc.; and Andrew

Russ, M.D. (collectively, Lincoln Medical) committed various torts when Russ

administered a COVID-19 vaccine to the child at a school clinic without parental

consent. Because we agree with the trial court that federal law confers

immunity on Lincoln Medical and preempts state law that would otherwise

allow Hogan to sue, we affirm the judgment.
2

I. BACKGROUND

[¶2] We draw the facts from Hogan’s notice of claim, viewed in the light

most favorable to Hogan. See Dutil v. Burns, 674 A.2d 910, 911 (Me. 1996). At

a school clinic held in November 2021, Lincoln Medical administered the

Pfizer-BioNTech mRNA COVID-19 vaccine to Jeremiah Hogan and Siara Jean

Harrington’s five-year-old child without having obtained parental consent to

the vaccination.

[¶3] On May 4, 2023, Hogan filed a notice of claim pursuant to the Maine

Health Security Act, see 24 M.R.S. § 2853 (2024), in the Superior Court against

the doctor who administered the vaccine (Russ), the corporation for which the

doctor worked (Lincoln Medical Partners), and that corporation’s parent

company (MaineHealth, Inc.). Framed as a multi-count civil complaint for

medical malpractice, Hogan’s notice alleged claims against all defendants on

behalf of the child for professional negligence, systemic professional

negligence, battery, and false imprisonment. The notice alleged three

additional tort claims against all defendants on behalf of the parents:

intentional infliction of emotional distress, negligent infliction of emotional

distress, and tortious interference with parental rights. Finally, the notice
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alleged negligent supervision against the corporate defendants on behalf of the

child and parents.

[¶4] After the court (Mullen, C.J.) appointed a chair for the prelitigation

screening panel, Lincoln Medical moved to dismiss the notice of claim, arguing

that it was immune from suit under the federal Public Readiness and

Emergency Preparedness (PREP) Act; see 42 U.S.C.A. §§ 247d-6d, 247d-6e

(Westlaw through Pub. L. No. 118-158). The screening panel chair ordered that

the matter be referred to the Superior Court for consideration of the motion.

[¶5] After receiving an opposing memorandum from Hogan and a reply

memorandum from Lincoln Medical, the court (Billings, J.) entered a judgment

on April 18, 2024, granting Lincoln Medical’s motion to dismiss. The court

interpreted the federal statute to provide immunity to each named defendant,

with no applicable exceptions.

[¶6] Hogan timely appealed. See 14 M.R.S. § 1851 (2024); M.R.

App. P. 2B(c)(1).

II. DISCUSSION

[¶7] We begin by summarizing the federal statutes at issue. The PREP

Act provides for immunity as follows:

Subject to the other provisions of this section, a covered person
shall be immune from suit and liability under Federal and State law
4

with respect to all claims for loss caused by, arising out of, relating
to, or resulting from the administration to or the use by an
individual of a covered countermeasure if a declaration under
subsection (b) has been issued with respect to such
countermeasure.

42 U.S.C.A. § 247d-6d(a)(1).1 “The immunity . . . applies to any claim for loss

that has a causal relationship with the administration to or use by an individual

of a covered countermeasure . . . .” Id. § 247d-6d(a)(2)(B). One “covered

countermeasure” is a drug or biological product “authorized for emergency

use” under specified statutes, including 21 U.S.C.A. § 360bbb-3 (Westlaw

through Pub. L. No. 118-158) (codification of section 564 of the Federal Food,

Drug and Cosmetics Act, added by Pub. L. No. 108-136 (Nov. 24, 2003)).

42 U.S.C.A. § 247d-6d(i)(1)(C). One type of “covered person” is “a qualified

person who prescribed, administered, or dispensed such countermeasure.” Id.

§ 247d-6d(i)(2)(B)(iv). “[A] licensed health professional or other individual

who is authorized to prescribe, administer, or dispense such countermeasures

under the law of the State in which the countermeasure was prescribed,

administered, or dispensed” is a “qualified person” under the statute. Id.

§ 247d-6d(i)(8)(A). The statute’s definition of “person” includes both

individuals and corporations. Id. § 247d-6d(i)(5).

1The term “loss” includes “any type of loss,” including emotional injury and the fear of injury.
42 U.S.C.A. § 247d-6d(a)(2)(A) (Westlaw through Pub. L. No. 118-158).
5

[¶8] For immunity to apply, the countermeasure must have been

administered to a member of the population specified in a declaration issued

by the Secretary of Health and Human Services to address the category of

disease specified in the declaration. Id. § 247d-6d(a)(3)(B), (a)(3)(C)(i), (b). It

must also have been administered during the declaration’s effective period and

in a location covered by the declaration. Id. § 247d-6d(a)(3)(A), (a)(3)(C)(ii).

[¶9] As an exception to the immunity conferred in § 247d-6d(a)(1),

Congress has authorized “an exclusive Federal cause of action against a covered

person for death or serious physical injury proximately caused by willful

misconduct . . . by such covered person.” Id. § 247d-6d(d)(1) (emphasis added).

For purposes of the statute, a “serious physical injury” is one that

(A) is life threatening;

(B) results in permanent impairment of a body function or
permanent damage to a body structure; or

(C) necessitates medical or surgical intervention to preclude
permanent impairment of a body function or permanent damage to
a body structure.

Id. § 247d-6d(i)(10). “[W]illful misconduct” under the statute is

an act or omission that is taken--

(i) intentionally to achieve a wrongful purpose;

(ii) knowingly without legal or factual justification; and
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(iii) in disregard of a known or obvious risk that is so great
as to make it highly probable that the harm will outweigh the
benefit.

Id. § 247d-6d(c)(1)(A).

[¶10] The plaintiff has “the burden of proving by clear and convincing

evidence willful misconduct by each covered person sued and that such willful

misconduct caused death or serious physical injury.” Id. § 247d-6d(c)(3). If a

person suffers serious physical injury or death, suit may generally not be

commenced until after the plaintiff has pursued recovery from a “Covered

Countermeasure Process Fund,” which is designed to compensate those who

have encountered adverse effects from countermeasures. Id. § 247d-6e(a),

(b)(1), (5)(A), (d)(1), (e)(3).

[¶11] The provision in the PREP Act conferring immunity on “covered

persons” includes a provision preempting conflicting state law:

Preemption of State law

During the effective period of a declaration under subsection (b),
or at any time with respect to conduct undertaken in accordance
with such declaration, no State or political subdivision of a State
may establish, enforce, or continue in effect with respect to a
covered countermeasure any provision of law or legal requirement
that--

(A) is different from, or is in conflict with, any requirement
applicable under this section; and
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(B) relates to the design, development, clinical testing or
investigation, formulation, manufacture, distribution, sale,
donation, purchase, marketing, promotion, packaging,
labeling, licensing, use, any other aspect of safety or efficacy,
or the prescribing, dispensing, or administration by qualified
persons of the covered countermeasure, or to any matter
included in a requirement applicable to the covered
countermeasure under this section or any other provision of
this chapter, or under the Federal Food, Drug, and Cosmetic
Act.

Id. § 247d-6d(b)(8).

[¶12] Hogan does not dispute either that the Secretary issued a

declaration or that the vaccine was administered by a qualified person as a

countermeasure during the time and in a location covered by the declaration.

See Declaration Under the Public Readiness and Emergency Preparedness Act

for Medical Countermeasures Against COVID-19, 85 Fed. Reg. 15,198

(Mar. 10, 2020). Having filed the claims in state court, Hogan cannot and does

not contend that the claims fall within the sole exception to the immunity

conferred in § 247d-6d(a)(1)—the authorized “exclusive Federal cause of

action against a covered person for death or serious physical injury proximately

caused by willful misconduct . . . by such covered person.” Id. § 247d-6d(d)(1).

The issue is therefore limited to whether the federal immunity statute
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immunizes Lincoln Medical against Hogan’s claims and preempts state law that

would otherwise allow a lawsuit.

[¶13] In general, “the construction of federal regulations or policies [is a]

matter[] of federal rather than state law.” Littlefield v. State, Dep’t of Hum. Servs.,

480 A.2d 731, 736 (Me. 1984). Thus, in determining whether the federal

immunity provision constrains state actions, we interpret the statute with the

goal “to effectuate the legislative intent and purposes of the United States

Congress.” Id.

[¶14] “The starting point in discerning congressional intent is the

existing statutory text . . . . It is well established that when the statute’s language

is plain, the sole function of the courts—at least where the disposition required

by the text is not absurd—is to enforce it according to its terms.” Lamie v. U.S.

Tr., 540 U.S. 526, 534 (2004) (quotation marks omitted); see also Wisconsin

Cent. Ltd. v. United States, 585 U.S. 274, 284 (2018) (“[W]ords generally should

be interpreted as taking their ordinary, contemporary, common meaning . . . at

the time Congress enacted the statute.” (quotation marks omitted)). “The

plainness or ambiguity of statutory language is determined by reference to the

language itself, the specific context in which that language is used, and the
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broader context of the statute as a whole.” Robinson v. Shell Oil Co., 519 U.S. 337,

341 (1997).

A. Immunity

[¶15] The language at issue here is plain, broad, and unambiguous with

respect to immunity from tort liability. A covered person is immune from suit

and liability under state law “with respect to all claims for loss caused by,

arising out of, relating to, or resulting from the administration” of the

emergency-authorized countermeasure—here, the vaccine. 42 U.S.C.A.

§ 247d-6d(a)(1); see id. § 247d-6d(i)(1)(C). The immunity “applies to any claim

for loss that has a causal relationship with the administration to . . . an

individual of” the vaccine. Id. § 247d-6d(a)(2)(B).

[¶16] Hogan alleges only injuries that were caused by the administration

of the vaccine. Even construed strictly because it is in derogation of the

common law, the immunity statute is clearly broad in scope. See Jamison v.

Encarnacion, 281 U.S. 635, 640 (1930) (“The rule that statutes in derogation of

the common law are to be strictly construed does not require such an

adherence to the letter as would defeat an obvious legislative purpose or lessen

the scope plainly intended to be given to the measure.”); Johnson v. S. Pac. Co.,

196 U.S. 1, 17 (1904) (“[C]onceding that statutes in derogation of the common
10

law are to be construed strictly, [t]hey are also to be construed sensibly, and

with a view to the object aimed at by the legislature.” (quotation marks

omitted)). We interpret the PREP Act’s immunity provision based on its plain

language and conclude that all defendants are immune from Hogan’s “claims

for loss caused by, arising out of, relating to, or resulting from the

administration” of the vaccine to the child. 42 U.S.C.A. § 247d-6d(a)(1). This

interpretation is consistent with other state appellate courts’ construction of

the immunity provision when parents alleged torts arising from a lack of

consent to vaccinate children. See Parker v. St. Lawrence Cnty. Pub. Health Dep’t,

954 N.Y.S.2d 259, 260-61, 263 (N.Y. App. Div. 2012); M.T. v. Walmart Stores, Inc.,

528 P.3d 1067, 1071, 1080-81 (Kan. Ct. App. 2023); de Becker v. UHS of Del., Inc.,

555 P.3d 1192, 1203 (Nev. 2024); Happel v. Guilford Cnty. Bd. of Educ., 899

S.E.2d 387, 389-90, 393-94 (N.C. Ct. App. 2024); Politella v. Windham Se. Sch.

Dist., 325 A.3d 88, 91-92, 98 (Vt. 2024).

[¶17] Hogan argues that this interpretation of federal law fails to

harmonize the statute with the Emergency Use Authorization (EUA) statutes

allowing the use of otherwise unapproved drugs or biological products that it

is reasonable to believe may be effective during a public health emergency

declared by the Secretary. See 21 U.S.C.A. § 360bbb-3(c). The PREP Act
11

references the EUA statute for purposes of explicitly including, within the scope

of the term “covered countermeasure,” a countermeasure authorized for

emergency use.2 42 U.S.C.A. § 247d-6d(i)(1)(C); 21 U.S.C.A. § 360bbb-3.

Accepting the allegations of the notice of claim as true, the provider’s failure to

obtain parental consent in this individual instance does not make the

administered vaccine—approved for emergency use under § 360bbb-3—any

less of a “covered countermeasure” under § 247d-6d(i)(1)(C).

[¶18] The PREP Act also does not, as Hogan asserts, violate international

law prohibiting non-consensual human medical experimentation. The

administration of a vaccine approved for emergency use is not an experiment

but an authorization to use a countermeasure that has been approved to

combat a public health emergency. See 21 U.S.C.A. § 360bbb-3. The notice of

claim alleges no facts, such as the subsequent monitoring or testing of the child,

that would suggest medical experimentation.3

2 The statute allowing EUAs requires the Secretary of Health and Human Services to establish
conditions on the authorization, to the extent practicable, “to ensure that individuals to whom the
product is administered are informed . . . of the option to accept or refuse administration of the
product.” 21 U.S.C.A. § 360bbb-3(e)(1)(A)(ii)(III) (Westlaw through Pub. L. No. 118-158). Although
the statute imposes a burden on the Secretary, it does not create a cause of action to enforce that
obligation, and in any event, Hogan has not sued the Secretary of Health and Human Services.

3 Although Hogan also contends that the immunity provision is, as applied, inconsistent with
constitutional principles of due process, the fundamental rights of parents to make decisions
regarding the care and management of their children, see Troxel v. Granville, 530 U.S. 57, 66 (2000),
are not absolute, see Dorr v. Woodard, 2016 ME 79, ¶ 13, 140 A.3d 467, and the federal government
has a compelling interest in legislating to address public health emergencies, see Roman Cath. Diocese
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B. Federal Preemption

[¶19] Hogan argues that the federal immunity statute has not preempted

state common law. “A conflict warranting preemption may be direct in that the

state regulation obviously contradicts federal regulation, or it may arise from

congressional intent, either express or implied, to occupy a particular area.”

State v. Lauriat, 561 A.2d 496, 496-97 (Me. 1989) (quotation marks omitted).

“Preemption, however, is not a favored concept, and federal regulation will be

deemed to be preemptive of state regulatory powers only if grounded in

persuasive reasons—either the nature of the regulated subject matter permits

no other conclusion or that Congress has unmistakably so ordained.” Id.

(quotation marks omitted).

[¶20] “In determining whether a federal law preempts a state law cause

of action, the determinative inquiry is ‘Congress’ intent in enacting the federal

statute at issue.’” Parker, 954 N.Y.S.2d at 261 (quoting Shaw v. Delta Air Lines,

of Brooklyn v. Cuomo, 592 U.S. 14, 18 (2020) (“Stemming the spread of COVID–19 is unquestionably
a compelling interest . . . .”). We reach the same conclusion whether the statute is subject to
rational-basis or strict-scrutiny review. See Jacobson v. Commonwealth of Massachusetts, 197 U.S. 11
(1905) (applying a rational-basis analysis to determine whether a state vaccine requirement was
constitutional); Pitts v. Moore, 2014 ME 59, ¶ 12 & n.3, 90 A.3d 1169 (setting forth the strict-scrutiny
standard requiring a compelling government interest for the government to interfere with the
fundamental right to parent). As to Hogan’s assertion that the immunity provision violates the child’s
constitutional right of bodily integrity, “[i]n the context of COVID-19, courts across the country have
concluded that Jacobson established that there is no fundamental right to refuse vaccination.”
Williams v. Brown, 567 F. Supp. 3d 1213, 1226 (D. Or. 2021); see also Norris v. Stanley, 567 F. Supp.
3d 818, 821 (W.D. Mich. 2021) (“Plaintiff is absolutely correct that she possesses those rights [to
privacy and bodily integrity], but there is no fundamental right to decline a vaccination.”).
13

Inc., 463 U.S. 85, 95 (1983)). “Where, as here, a federal law contains an express

preemption clause, “[the] ‘focus [is] on the plain wording of the clause, which

necessarily contains the best evidence of Congress’ preemptive intent.’” Id.

(quoting Chamber of Com. of U.S. v. Whiting, 563 U.S. 582, 594 (2011)).

[¶21] The statute at issue here plainly provides that no state may

“enforce” or “continue in effect” laws that “relate[] to” the administration of

covered countermeasures by qualified persons and differ from or conflict with

the federal statute. 42 U.S.C.A. § 247d-6d(b)(8). The Supreme Court has

recognized that “the phrase ‘relate to’ in a preemption clause ‘express[es] a

broad pre-emptive purpose.’” Coventry Health Care of Mo., Inc. v. Nevils, 581 U.S.

87, 95-96 (2017) (quoting Morales v. Trans World Airlines, Inc., 504 U.S. 374,

383 (1992)). Although Hogan is correct that there are limits on the extent to

which a state law will be regarded as “relat[ing] to” a specific federal measure,

see N.Y. State Conf. of Blue Cross & Blue Shield Plans v. Travelers Ins. Co., 514 U.S.

645, 655-56 (1995) (quotation marks omitted), Maine’s common law torts

clearly fall within the PREP Act’s prohibition to the extent that they allow

recovery for claims against defendants administering vaccines who, under the

federal statute, are immune from suit or liability, see 42 U.S.C.A.

§ 247d-6d(a)(1), (b)(8).
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The entry is:

Judgment affirmed.

F.R. Jenkins, Esq. (orally), Meridian 361 International Law Group, PLLC,
Portland, and David E. Bauer, Esq., Portland, for appellants Jeremiah Hogan,
Siara Jean Harrington, and their child

Devin W. Deane, Esq., Noah D. Wuesthoff, Esq., and Joseph M. Mavodones, Esq.
(orally), Norman, Hanson & DeTroy, LLC, Portland, for appellees Lincoln
Medical Partners, MaineHealth, Inc., and Andrew Russ

Lincoln County Superior Court docket number CV-2023-13
FOR CLERK REFERENCE ONLY

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