Brian Elkins v. Southeastern Indiana Health Management Inc.
CourtCourt of Appeals for the Seventh Circuit
Date FiledOctober 20, 2026
Docket23-3159
JudgeLee
StatusPublished
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Full Opinion
In the
United States Court of Appeals
For the Seventh Circuit
____________________
No. 23-3159
BRIAN ELKINS and ANNIE ELKINS,
Plaintiffs-Appellees,
v.
SOUTHEASTERN INDIANA HEALTH MANAGEMENT INC., doing
business as COLUMBUS REGIONAL HEALTH,
Defendant-Appellant.
____________________
No. 23-3175
KAITLIN LAMARR,
Plaintiff-Appellee,
v.
GOSHEN HEALTH SYSTEM, INC., d/b/a GOSHEN HEALTH,
Defendant-Appellant.
____________________
2 Nos. 23-3159, 23-3175, 23-3363 & 23-3385
No. 23-3363
JENNIFER FLEECE,
Plaintiff-Appellee,
v.
BOARD OF TRUSTEES OF THE HANCOCK REGIONAL HOSPITAL,
Defendant-Appellant.
____________________
No. 23-3385
KEITH CHIARO and JANE DOE,
Plaintiffs-Appellees,
v.
METHODIST HOSPITALS, INC.,
Defendant-Appellant.
____________________
Appeals from the United States District Court for the
Southern District of Indiana, Indianapolis Division.
Nos. 1:23-cv-1117 & 1:23-cv-1173 — James R. Sweeney, II, Chief Judge,
No. 1:23-cv-1235 — Matthew P. Brookman, Judge,
No. 1:23-cv-1051 — Sarah Evans Barker, Judge.
____________________
ARGUED MAY 28, 2024 — DECIDED OCTOBER 20, 2026
____________________
Nos. 23-3159, 23-3175, 23-3363 & 23-3385 3
Before JACKSON-AKIWUMI, LEE, and KOLAR, Circuit Judges.
LEE, Circuit Judge. Brian and Annie Elkins are patients at
Columbus Regional Health (“CRH”), 1 a health system serving
ten counties in southeastern Indiana. They allege that a Face-
book tracking software called the “Meta Pixel” embedded in
CRH’s online webpage shared their health data without their
consent. The Elkinses brought this putative class action suit in
Indiana state court claiming that CRH violated various state
laws when it shared their health data. CRH subsequently re-
moved the suit to federal court by invoking the federal officer
removal statute, 28 U.S.C. § 1442(a)(1), as the basis for federal
jurisdiction. Section 1442(a)(1) gives federal courts subject
matter jurisdiction over cases brought against the United
States, federal agencies, federal officers, and persons “acting
under” a federal officer. 28 U.S.C. § 1442(a)(1). To claim fed-
eral jurisdiction, CRH insisted it was “acting under” the De-
partment of Health and Human Services (“HHS”) when it cre-
ated its online patient portals.
The district court rejected CRH’s jurisdictional argument
and remanded the case to Indiana state court. CRH appealed,
and the case was consolidated with four nearly identical law-
suits against health care providers claiming federal jurisdic-
tion under § 1442(a)(1). In each of those cases, the district
court had similarly rejected the provider’s § 1442(a)(1) juris-
dictional argument. Because we agree with the district courts
that the health care providers were not “acting under” the
1 Although the health system does business as Columbus Regional
Health, its legal name is Southeastern Indiana Health Management, Inc.
4 Nos. 23-3159, 23-3175, 23-3363 & 23-3385
federal government when they created their patient portals,
we affirm.
I. Background
In 2009, Congress enacted the Health Information Tech-
nology for Economic and Clinical Health (“HITECH”) Act.
See Pub. L. No. 111-5, 123 Stat. 264 (Feb. 17, 2009) (codified at
42 U.S.C. § 300jj-11 et seq.). To encourage health care providers
to adopt health information technology, including the use of
electronic health records (“EHRs”), the HITECH Act directed
HHS to make incentive payments to any Medicare-participat-
ing provider who was a “meaningful EHR user.” 42 U.S.C.
§ 1395w-4(o)(1)(A)(i). Then, starting in 2015, the Act required
HHS to reduce Medicare reimbursements to any provider
who failed to meet the program’s requirements. Id. § 1395w-
4(a)(7)(A)(i).
The Centers for Medicare and Medicaid Services (“CMS”)
promulgated regulations to implement the HITECH Act in
2010. Medicare and Medicaid Programs; Electronic Health
Record Incentive Program, 75 Fed. Reg. 44,314 (July 28, 2010)
(codified at 42 C.F.R. pts. 412, 413, 422, and 495). These regu-
lations created the Meaningful Use Program, which estab-
lishes several objectives providers must meet to qualify as
“meaningful EHR users” under the HITECH Act and thus
avoid the reductions in Medicare reimbursements described
above. 42 C.F.R. §§ 495.2–495.370.
One objective directed health care providers to “provide[]
patients … with timely electronic access to their health infor-
mation.” Id. § 495.24(d)(5)(i)(A). To meet this objective, pro-
viders established online patient portals where patients could
Nos. 23-3159, 23-3175, 23-3363 & 23-3385 5
access their EHRs and communicate with their health care
providers.
In 2023, Brian and Annie Elkins brought this class action
suit against CRH, asserting claims for breach of implied con-
tract and unjust enrichment as well as violations of the Indi-
ana Deceptive Consumer Sales Act, Ind. Code § 24-5-0.5-1
(2006), and the Indiana Wiretapping Act, Ind. Code § 35-33.5-
5-5 (2014). Defendants timely removed to federal court, as-
serting federal subject matter jurisdiction pursuant to
§ 1442(a)(1). To fit within its parameters, the health care pro-
viders alleged they were “acting under” the federal govern-
ment when they created and maintained their patient portals
in accordance with CMS’s Meaningful Use Program.
The Elkinses moved to remand the suit to state court, and
the district court granted their motion. The court concluded
CRH was not “acting under” a federal officer when it created
its patient portal because, although CRH was highly regu-
lated, its “patient portal is not something the government
‘needs.’” It also determined that, unlike the work of certain
private government contractors, maintaining private patient
EHRs is not a “basic governmental task.” CRH appealed.
Before the parties submitted their appellate briefs, they
jointly moved to consolidate their appeal with four other ap-
peals also pending before this court pursuant to Federal Rule
of Appellate Procedure 27. See App. Dkt. 14. 2 Each of the four
additional cases brought nearly identical allegations against
2 The four other appeals are: Lamarr v. Goshen Health System, Inc. (23-
3175), Doe v. Sarah Bush Lincoln Health Center (23-3340) (appeal dismissed),
Fleece v. Board of Trustees of the Hancock Regional Hospital (23-3363), and Chi-
aro v. The Methodist Hospitals, Inc. (23-3385).
6 Nos. 23-3159, 23-3175, 23-3363 & 23-3385
health care providers in Indiana and Illinois. They also pre-
sented the same legal question before us here.
We granted the parties’ motion to consolidate and in-
structed them to submit a single appellants’ brief, a single ap-
pellees’ brief, and a single reply brief. See App. Dkt. 16. Given
that this is a consolidated appeal, our holding applies equally
to all four appeals.
II. Discussion
We have appellate jurisdiction to review the remand or-
ders pursuant to 28 U.S.C. § 1447(d). See BP P.L.C. v. Mayor &
City Council of Balt., 593 U.S. 230 (2021). “We review subject-
matter jurisdiction and the propriety of the removal of a state-
court action de novo.” Baker v. Atl. Richfield Co., 962 F.3d 937,
941 (7th Cir. 2020) (quoting Betzner v. Boeing Co., 910 F.3d 1010,
1014 (7th Cir. 2018)). The burden of establishing federal juris-
diction is on the party seeking removal. Id.
Removal pursuant to § 1442(a)(1) is appropriate when
“the defendant (1) is a person within the meaning of the stat-
ute, (2) is acting under the United States, its agencies, or its
officers, (3) is acting under color of federal authority, and (4)
has a colorable federal defense.” Id. (quoting Betzner, 910 F.3d
at 1015). This case turns on the second element: whether the
health care providers were “acting under” the United States,
its agencies, or its officers. More specifically, the question for
us is whether the providers were “acting under” HHS when
they created their online patient portals and accepted federal
incentive payments for doing so.
“The words ‘acting under’ are broad … and the statute
must be ‘liberally construed.’” Watson v. Philip Morris Cos.,
Inc., 551 U.S. 142, 147 (2007) (quoting Colorado v. Symes, 286
Nos. 23-3159, 23-3175, 23-3363 & 23-3385 7
U.S. 510, 517 (1932)). Still, the statute’s “broad language is not
limitless,” and “a liberal construction nonetheless can find
limits in a text’s language, context, history, and purposes.” Id.
As the Supreme Court has observed, the “acting under”
relationship “typically involves ‘subjection, guidance, or con-
trol.’” Id. at 151 (quoting Webster’s New International Diction-
ary 2765 (2d ed. 1953)). In addition, “the private person’s ‘act-
ing under’ must involve an effort to assist, or to help carry out,
the duties or tasks of the federal superior.” Id. at 152.
A. Cases Interpreting § 1442(a)(1)
We begin with the Supreme Court’s decision in Watson.
There, consumers brought a class action against cigarette
manufacturer Philip Morris alleging the company’s advertise-
ments and packaging violated Arkansas’s unfair business
practice laws. Id. at 146. Philip Morris removed the suit to fed-
eral court pursuant to § 1442(a)(1), claiming it “acted under”
the Federal Trade Commission (“FTC”) based on the FTC’s
“detailed supervision of the cigarette testing process.” Id. at
147. The Supreme Court rejected this argument, explaining
that “acting under” the federal government “does not include
simply complying with the law.” Id. at 152. “[T]hough we find
considerable regulatory detail and supervision,” the Court
continued, “we can find nothing that warrants treating the
FTC/Philip Morris relationship as distinct from the usual reg-
ulator/regulated relationship.” Id. at 157.
Philip Morris’s regulatory relationship with the FTC was
different, the Supreme Court explained, from that of a private
contractor that “help[s] the Government to produce an item
that it needs.” Id. at 153. This is because, in such instances, a
private contractor “goes beyond simple compliance with the
8 Nos. 23-3159, 23-3175, 23-3363 & 23-3385
law and helps officers fulfill other basic governmental tasks.”
Id. For example, a chemical company that produced Agent
Orange for the Department of Defense to conduct a war was
“acting under” the agency since it was arguably “per-
form[ing] a job that … the Government itself would have had
to perform.” Id. at 154 (citing Winters v. Diamond Shamrock
Chemical Co., 149 F.3d 387 (5th Cir. 1998)).
We have relied on Watson’s reasoning to find federal juris-
diction in several cases where the removing party contracted
with the United States to manufacture goods during wartime.
In Ruppel v. CBS Corporation, for example, we held that a man-
ufacturer was “acting under” the federal government when it
produced turbines for an aircraft carrier according to govern-
ment specifications. 701 F.3d 1176, 1181 (7th Cir. 2012) (‘“’Act-
ing under’ covers situations, like this one, where the federal
government uses a private corporation to achieve an end it
would have otherwise used its own agents to complete.”).
Likewise, in Betzner, we found that a manufacturer fell under
the removal statute when it “contracted to manufacture heavy
bomber aircraft for the United States Air Force” and “acted
under the military’s detailed and ongoing control.” 910 F.3d
at 1015. Finally, in Baker, we concluded the defendant was
“acting under” the federal government when it provided the
government with raw materials during World War II and
manufactured those materials under the government’s con-
tinuous supervision and according to detailed specifications.
962 F.3d at 943.
By contrast, we have declined to extend federal jurisdic-
tion in cases similar to Watson where the conduct at issue was
“regulation, not delegation.” 551 U.S. at 157. In Martin v. Pe-
tersen Health Operations, LLC, the estate of a deceased nursing
Nos. 23-3159, 23-3175, 23-3363 & 23-3385 9
home resident sued the nursing home for its failure to take
adequate precautions during the COVID-19 pandemic. 37
F.4th 1210, 1212 (7th Cir. 2022). To support federal jurisdic-
tion, the nursing home claimed it was “acting under” a federal
officer in accordance with § 1442(a)(1), because it was heavily
regulated by the federal government. Id. Although we
acknowledged that the nursing home was “subject to exten-
sive federal regulation,” we observed that “regulation does
not turn a private entity into a public actor.” Id. at 1212–13.
We therefore concluded that the nursing home was more akin
to the cigarette manufacturers in Watson—highly regulated
but not “acting under” an officer or agent of the United States
pursuant to § 1442(a)(1). Id. at 1213.
B. Application to Defendants
For much the same reasons, we conclude that the health
care providers here did not “act under” an officer or agency
of the federal government when they created their patient
health portals. Like the cigarette manufacturer in Watson and
the nursing home in Martin, the health care providers merely
complied with federal regulations when establishing and
maintaining their patient portals. And, even though an entity
may be “subject to extensive federal regulation,” such regula-
tion “does not turn a private entity into a public actor.” Mar-
tin, 37 F.4th at 1212–13.
Defendants insist that their relationship with the federal
government went beyond regulation because—unlike in Wat-
son or Martin—they were completing a “fundamental federal
governmental task” by creating patient portals. We disagree.
When the health care providers construct and operate their
patient portals, they are not doing the government’s business.
The patient portals are private websites designed by private
10 Nos. 23-3159, 23-3175, 23-3363 & 23-3385
actors. Once the patient portals are up and running, it is the
providers and their patients who benefit from them most di-
rectly—not the federal government.
To be sure, the patient portals advance government policy
by making EHRs more accessible. But a private party does not
accomplish a basic government task every time it acts in re-
sponse to a government incentive. Indeed, “[p]rivate firms re-
tain their private character even when many aspects of their
conduct are controlled by federal statutes and rules.” See Mar-
tin, 37 F.4th at 1213. Regardless of any federal incentive, the
patient portals are still private websites built by private health
care providers to serve their own patients and staff.
The health care providers were not “acting under” the fed-
eral government for a second reason. To qualify for federal
jurisdiction pursuant to § 1442(a)(1), a private entity must
have an “unusually close” relationship to a federal superior
“involving detailed regulation, monitoring, or supervision.”
Watson, 551 U.S. at 153. This was the case in our military con-
tractor cases. For example, in Ruppel, the defendant claimed
that it “supplied asbestos under the Navy’s direction and in
accordance with detailed Navy specifications, the Navy
closely controlled the process, and the Navy was aware of as-
bestos’s health hazards.” 701 F.3d at 1179. Here, by contrast,
Defendants lack the same “unusually close” relationship with
the federal government.
Indeed, the Meaningful Use regulations do not provide
any details as to how Defendants were to maintain their online
patient portals. Instead, the relevant version of the regulations
only required that they generally “provide patients the ability
to view online, download, and transmit their health
Nos. 23-3159, 23-3175, 23-3363 & 23-3385 11
information within four days of the information being availa-
ble to the [eligible professional].” 42 C.F.R. § 495.20(d)(12)(i)(B).
Perhaps recognizing the lack of specificity in the regula-
tions, Defendants point to several lines in the “Patient En-
gagement Playbook” published by the Office of the National
Coordinator for Health Information Technology. But the Play-
book is not binding on providers. To the contrary, the Play-
book describes itself as merely a “compilation of tips and best
practices … from clinicians and health systems.” See Off. of the
Nat’l Coordinator for Health Info. Tech., The ONC Patient En-
gagement Playbook, HealthIT.gov, https://www.healthit.gov/play-
book/pe/ (emphases added). Then, in the Playbook’s intro-
duction, it states, “[we] hope you’ll use [the Playbook] in a way
that works for you and your practice.” Id. (emphasis added).
Such nonbinding recommendations about patient portal
development are a far cry from the detailed government spec-
ifications typically required to establish the unusually close
relationship required for jurisdiction under § 1442(a)(1). See
Betzner, 910 F.3d at 1015–16 (finding defendant was “acting
under” the federal government because it manufactured
bomber aircraft “under the detailed and ongoing direction
and control of the United States military”); cf. Panther Brands,
LLC v. Indy Racing League, LLC, 827 F.3d 586, 590 (7th Cir.
2016) (concluding that the relationship between a private
marketing agent and the Army National Guard “fell far short
of the closely monitored and highly regulated relationship[]”
required to establish jurisdiction under § 1442(a)(1)).
In concluding that Defendants cannot satisfy § 1442(a)(1),
we join a number of our sister circuits that have reasoned the
same. See, e.g., Doe v. BJC Health Sys., 89 F.4th 1037 (8th Cir.
2023) (“The design of private websites is not—and has never
12 Nos. 23-3159, 23-3175, 23-3363 & 23-3385
been—a basic governmental task.”); Mohr v. Trs. of Univ. of Pa.,
93 F.4th 100, 105 (3d Cir. 2024) (acknowledging that the pro-
vider “does advance the government’s policy by operating a
patient portal” but concluding that doing so is “mere compli-
ance” with federal law); Martin v. LCMC Health Holdings, Inc.,
101 F.4th 410, 415 (5th Cir. 2024) (“LCMC’s mere compliance
with the Meaning[ful] Use regulations does not mean that
LCMC acted pursuant to a federal officer’s directive.”); Doe v.
Cedars-Sinai Health Sys., 106 F.4th 907, 917 (9th Cir. 2024)
(“[The HITECH] Program's requirements do not show an ex-
press delegation of authority to Cedars-Sinai to accomplish a
basic governmental task on the National Coordinator's be-
half.”); Doe v. Integris Health, Inc., 123 F.4th 1189, 1196 (10th
Cir. 2024) (“[T]he government does not require Integris to use
trackers or otherwise control how Integris provides access to
EHR. As a result, Integris is not ‘acting under’ a federal of-
ficer.”). And we see no reason to disagree with their analysis.
In sum, Defendants were not “acting under” a federal of-
ficer or agency when they created their patient portals. 3 The
CDC’s Meaningful Use regulations may have incentivized
them to create online patient portals, but these incentives are
“regulation, not delegation.” Watson, 551 U.S. at 157.
* * *
For the foregoing reasons, the judgments of the district
courts are AFFIRMED.
3 Because we hold that Defendants did not act under federal authority
when they created their patient portals, we do not reach whether their
conduct “relates to” their exercise of federal authority or whether they
have a colorable federal defense.