concluding that in order for failure to disclose a material fact to constitute a deceptive act under the Kansas Consumer Protection Act,9 “there must be a duty to disclose the fact”
How later courts described this case
- concluding that in order for failure to disclose a material fact to constitute a deceptive act under the Kansas Consumer Protection Act,9 “there must be a duty to disclose the fact”
- noting “the settled premise that a seller generally has no duty to disclose internal pricing policies or its method for valuing what it sells”
- holding that the plaintiff failed to properly allege the elements of a FDUTPA claim where the “express terms of the reservation agreement” undermined the claim that the agreement was deceptive
- holding that the relevant standard “requires a showing of probable, not possible, deception.”
Written by the judges who cited it.
The opinion
IN THE UNITED STATES DISTRICT COURT
FOR THE MIDDLE DISTRICT OF NORTH CAROLINA
NATHANIEL J. NOLAN and HELENA )
WITTENBERG, individually and )
on behalf of all others )
similarly situated, )
)
Plaintiffs, )
)
v. ) 1:21cv979
)
LABORATORY CORPORATION OF )
AMERICA HOLDINGS, )
)
Defendant. )
MEMORANDUM OPINION AND ORDER
THOMAS D. SCHROEDER, Chief District Judge.
This is a putative class action involving claims of unfair
and deceptive conduct under Nevada and Florida law related to the
billing practices of Defendant Laboratory Corporation of America
Holdings (“Labcorp,” sometimes referred to the parties as
“LabCorp”).1 Before the court is Labcorp’s motion to dismiss all
claims pursuant to Federal Rule of Civil Procedure 12(b)(6).
(Docs. 10, 11.) Plaintiffs filed a response in opposition (Doc.
13), and Defendant replied (Doc. 15). On November 8, 2022, the
court heard oral argument. For the reasons set forth below, the
motion to dismiss for failure to state a claim will be granted,
1 Plaintiffs allege this case is related to a separate putative class
action against Labcorp, Anderson v. Laboratory Corp. of Am. Holdings,
No. 1:17-cv-193 (M.D.N.C.).
and the complaint will be dismissed.
I. BACKGROUND
The allegations of the complaint, viewed in the light most
favorable to Plaintiffs as the non-moving parties, show the
following:
LabCorp provides laboratory testing services to millions of
healthcare recipients internationally. (Doc. 1 ¶ 27.) It has
more than 100 million patient encounters annually and “typically
processes clinical lab tests on more than 3 million patient
specimens per week.” (Id. ¶ 12.) “Labcorp Diagnostics,” one of
Labcorp’s two major business segments, is an independent clinical
laboratory business that provides the services that are the subject
of Plaintiffs’ complaint. (Id. ¶ 28-29.) Labcorp Diagnostics
offers an array of frequently requested and specialty testing
through a network of primary and specialty laboratories. (Id.)
Its customers are managed care organizations, biopharmaceutical
companies, governmental agencies, physicians and other healthcare
providers, hospitals, employers, patients, and consumers.
(Id. ¶ 31.)
Labcorp routinely performs lab testing services prior to
processing billing information and determining the ultimate amount
due. (Id. ¶¶ 21, 48.) It later determines the price and the
paying party’s information upon receiving (i) a medical diagnosis
code and test code for each lab test prescribed by a physician,
and (ii) the patient’s insurance information (for insured
patients). (Id.) If the service is covered by a patient’s health
insurance plan, Labcorp bills the third-party payer the “health
plan allowed” rate.2 (Id. ¶¶ 21-22, 48, 55.) If the service is
not covered by the patient’s health insurance plan, Labcorp bills
the patient directly at the “patient list price” (hereinafter “list
price”). (Id. ¶¶ 21-22.) These rates vary greatly, but the list
price tends to be much higher than the health plan allowed rate.
(Id.) Accordingly, if a patient’s insurer denies coverage for
certain lab testing services, the patient will generally owe
Labcorp the much higher list price. (Id. ¶¶ 4-5, 9-10.)
Typically, a patient will authorize his or her physician to
order lab testing without inquiring as to what lab will perform
the work. In this situation, the patient’s healthcare provider
will generally collect the specimen necessary for testing, e.g.,
perform a blood-draw, and then send that specimen to a Labcorp
location for testing. (Id. ¶ 21.) In some instances, however, a
patient will go directly to a Labcorp “patient service center” or
other Labcorp facility to have the lab-testing services performed.
2 Even though Labcorp bills the third-party payer, e.g., the patient’s
insurer, the patient is usually responsible for paying all or part of
the health plan allowed rate directly to Labcorp because the cost of the
lab testing services frequently does not exhaust the patient’s health
insurance deductible. (Doc. 1 ¶ 69.) Thus, the health plan allowed
rate generally corresponds to what the patient owes out-of-pocket (at
least when the pertinent lab testing services are covered by the
patient’s health insurance plan). (Id. ¶¶ 21-22, 48, 69.)
(Id. ¶¶ 29, 66, 100-101.) Before it will perform any lab testing
services, however, Labcorp asks its patients to review and sign a
document - the Patient Acknowledgement of Estimated Financial
Responsibility form (the “Patient Acknowledgement”) (Id. ¶¶ 1, 3-
4, 7; Doc. 1-1; Doc. 1-2; Doc. 1-3.)
The Patient Acknowledgment - which forms the basis of
Plaintiffs’ complaint - is a “common form used throughout Labcorp’s
operations and is signed by thousands, if not millions” of patients
a year. (Id. ¶ 12.) It provides insured patients with an estimate
of the total amount due for the lab-testing services, assuming
those services are covered by their health insurance plan. Put
differently, the Patient Acknowledgment gives patients an estimate
of what they will owe out-of-pocket, reflecting the estimated
deductible, coinsurance, and copay amounts if the lab-testing
services provided are covered by their health insurance plan. (Id.
¶¶ 1, 3, 73, 112; Doc. 1-1, Doc. 1-2, Doc. 1-3.) The Patient
Acknowledgment refers to this cost estimate as the “health plan
allowed rate.” (Id.) It also sets out the “Estimated Amount Paid
by Health Plan.” (Id.) The form has a block on page two entitled,
“YOUR ESTIMATED RESPONSIBILITY” with a dollar amount provided.
(Id.) What the Patient Acknowledgement does not provide is the
(generally more expensive) list price - the amount a patient would
owe in the event the services are not covered by her health
insurance. (Id. ¶ 74; Doc 1-1, Doc. 1-2, Doc. 1-3.)
The second page of the Patient Acknowledgment includes
further information about the estimate’s conditional nature. In
full, it reads:
You are being provided with this Acknowledgment of
Estimated Financial Responsibility. This estimate
assumes all services will be covered. Your physician
has requested the above service(s) and some services may
be considered investigational, require prior
authorization, are excluded or otherwise not covered by
your health plan. Additionally, your physician may have
requested laboratory services that will automatically
trigger additional testing procedures based on certain
clinical indications or your physcian may determine it
necessary to order additional testing procedures based
on the sample collected today. LabCorp will bill you
for any additional testing. Your health plan may not
pay for these services and you will be personally
responsible for payment for these services. This
acknowledgment is based on the health plan information
provided at the time of service. In the event that your
information changes, your acknowledgment of financial
responsibility still applies.
By signing below, you acknowledge: I want the laboratory
test(s) listed above to be performed. My health plan
will be billed for the applicable charges. As outlined
above, I understand that my health plan may not pay for
this test(s) at 100%. The amount I may have to pay may
be different than the estimated amount. I agree to be
personally and fully responsible for charges from
today’s services that are not covered by my health plan.
(Doc. 1-1 at 2 (bold added); Doc. 1-2 at 2 (bold added); Doc. 1-3
at 2 (bold added).) Thus, by signing the Patient Acknowledgment,
the patient agrees that her “health plan may not pay for this
test(s) at 100%” and that the amount the patient “may have to pay
may be different than the estimated amount.”
Plaintiffs Nathaniel Nolan and Helena Wittenberg complain
that that the Patient Acknowledgement is materially misleading and
deceptive under their respective state’s law because it discloses
the health plan allowed rate without also disclosing the patient’s
list price – the amount due in the event the test is not covered
by insurance.
A. Plaintiff Nolan
On September 11, 2018, Plaintiff Nolan visited a Labcorp
facility in Reno, Nevada, to have several lab tests performed.
(Doc. 1 ¶¶ 64-66.) Before Labcorp would administer the tests,
however, a Labcorp representative required Nolan to sign the
Patient Acknowledgment, which included an estimate of the health
plan allowed rate that Nolan would owe assuming each test was
covered by his insurance. (Id. ¶ 67; Doc. 1-1 at 1.) Nolan signed
and dated the Patient Acknowledgment, thereby agreeing “to be
personally and fully responsible for charges” for those lab-
testing services not covered by his health plan. (Doc. 1 ¶ 73,
Doc. 1-1 at 2.) One of the tests was a Vitamin D, 25-hydroxy test,
which the health plan allowed rate estimated would cost him $18.93.
(Doc. 1 ¶ 4, 68; Doc. 1-1 at 1.) The Patient Acknowledgement did
not include the list price of the Vitamin D (or any other) test,
“or that the list price is many multiples of the disclosed
negotiated rate.” (Doc. 1 ¶ 74.)
Two weeks later, Labcorp sent Nolan a bill, which charged him
$292 for the Vitamin D test. (Id. ¶¶ 5, 75-79.) Unable to
understand the discrepancy between the bill ($292) and the Patient
Acknowledgement ($18.93), Nolan requested and received an
Explanation of Benefits (“EOB”) from Highmark Blue Shield, his
insurer. (Id. ¶ 77.) Highmark explained that although Nolan’s
insurance plan covered each of the other tests, it did not cover
the Vitamin D test. (Id. ¶ 78.) Accordingly, the EOB stated that
Nolan would be responsible for paying Labcorp the Vitamin D list
price of $292 (in addition to the health plan allowed rate for
each of the other tests Nolan was administered, because Nolan had
not met his copay or deductible). (Id.) Nolan was “shocked”
because he assumed, based on the Patient Acknowledgment, that
Labcorp was willing to perform the test for the “Health Plan
Allowed Rate” of $18.93. (Id. ¶ 79.) Nolan has since refused to
pay the list price for the test “absent an appropriate settlement
of his claim.” (Id. ¶ 5.)
B. Plaintiff Wittenberg
Plaintiff Wittenberg’s experience is similar. On April 16,
2018, Wittenberg went to a Labcorp patient service center in Lake
Mary, Florida, where she was administered two different sets of
clinical laboratory tests. (Id. ¶¶ 7-8, 100.) Wittenberg signed
a Patient Acknowledgement for each set of tests. (Doc. 1 ¶¶ 7,
101, 106, 109; Doc. 1-2 at 2; Doc. 1-3 at 2.) The total estimated
responsibility, based on the “Health Plan Allowed Rate” for the
first set of tests provided a cost estimate of $44.60 (Doc. 1 ¶¶ 7,
101, 106; Doc. 1-2 at 1) and $65.27 for the second set (id. ¶¶ 9,
101, 109, Doc. 1-3 at 1); the totals for both estimates reflected
that the full expense was within the applicable deductible.
Subsequently, Wittenberg received an EOB from her insurer.
(Doc. 1 ¶ 116.) It stated that because Labcorp was out of network
with her insurance plan, she might be held responsible for “any
charges in excess of the maximum amount.” (Id.) Shortly
thereafter, Wittenberg received two invoices from Labcorp, each
corresponding to the set of lab tests she received in April. (Id.
¶¶ 117, 119.) The invoices revealed that, because her insurance
was out of network with Labcorp, none of the tests she received
was covered; as a result, Labcorp charged her the list price rather
than the health plan allowed rate for each test. (Id. ¶¶ 9, 116-
122.) The first invoice showed that Wittenberg owed Labcorp a
total of $335 for the first set of tests, as opposed to the $44.60
estimate disclosed on the Patient Acknowledgment. (Id. ¶¶ 8-9,
117-18.) The second invoice showed that she owed a total of $650
for the second set of tests, as opposed to the $65.27 Patient
Acknowledgement estimate. (Id. ¶¶ 8-9, 119-120.) Wittenberg has
since paid Labcorp only the health plan allowed rate stated on the
Patient Acknowledgment, plus “$140 towards the [outstanding] cost
of each bill.” (Id. ¶ 10.) She has otherwise refused to pay the
patient list prices “absent an appropriate settlement of her
claim.” (Id.)
On December 29, 2021, Plaintiffs Nolan and Wittenberg filed
the present putative class action. In Count I, Nolan alleges that
Labcorp has engaged in unfair or deceptive trade practices by
improperly billing for lab testing services in violation of the
Nevada Deceptive Trade Practices Act (“NDTPA”), Nev. Rev. Stat.
§ 598.0903 et seq. (Id. ¶¶ 153-59.) In Count II, Wittenberg
alleges that Labcorp has engaged in “unfair methods of competition,
unconscionable acts or practices, and unfair or deceptive acts or
practices” in violation of the Florida Deceptive and Unfair Trade
Practices Act (“FDUTPA”), Fla. Stat. Ann. § 501.201, et seq. (Id.
¶¶ 160-66.) Nolan, a resident of Nevada, and Wittenberg, a
resident of Florida, seek to certify a class of all persons
residing in each state who signed a Patient Acknowledgment
disclosing the “Estimated Charges” for lab services but were billed
a patient list price that exceeded the disclosed health plan
allowed rate for those services. (Id. ¶¶ 142, 153-59, 160-66.)
Labcorp now moves to dismiss the complaint pursuant to Federal
Rule of Civil Procedure 12(b)(6), largely on the basis that there
“is nothing misleading, false, deceptive, or unfair” about the
Patient Acknowledgment because, by its explicit terms, it merely
provides an estimate “assuming that all services will be covered
by the patient’s health plan.” (Doc. 11 at 1-2.) Plaintiffs argue
in response that Labcorp’s use of the Patient Acknowledgment is
deceptive because Labcorp knows that its patients might owe higher
list prices but “makes a conscious decision not to disclose them.”
(Doc. 13 at 10).
II. ANALYSIS
A. Standard of Review
Federal Rule of Civil Procedure 8(a)(2) provides that a
complaint must contain “a short and plain statement of the claim
showing that the pleader is entitled to relief.” Fed. R. Civ. P.
(8)(a)(2). Under Federal Rule of Civil Procedure 12(b)(6), “a
complaint must contain sufficient factual matter . . . to ‘state
a claim to relief that is plausible on its face.’” Ashcroft v.
Iqbal, 556 U.S. 662, 678 (2009) (quoting Bell Atl. Corp. v.
Twombly, 550 U.S. 544, 570 (2007)). A claim is plausible “when
the plaintiff pleads factual content that allows the court to draw
the reasonable inference that the defendant is liable for the
misconduct alleged.” Id.
A motion to dismiss under Rule 12(b)(6) is meant only to
“test[] the sufficiency of a complaint” and not to “resolve
contests surrounding the facts, the merits of a claim, or the
applicability of defenses.” Republican Party of N.C. v. Martin,
980 F.2d 943, 952 (4th Cir. 1992). Thus, in considering a Rule
12(b)(6) motion, a court “must accept as true all of the factual
allegations contained in the complaint,” Erickson v. Pardus, 551
U.S. 89, 94 (2007) (per curiam), and all reasonable inferences
must be drawn in the plaintiff’s favor. Ibarra v. United States,
120 F.3d 472, 474 (4th Cir. 1997).
“Rule 12(b)(6) protects against meritless litigation by
requiring sufficient factual allegation ‘to raise a right to relief
above the speculative level’ so as to ‘nudge[] the[] claims across
the line from conceivable to plausible.’” Sauers v. Winston-
Salem/Forsyth Cty. Bd. Of Educ., 179 F. Supp. 3d 544, 550 (M.D.N.C.
2016) (alterations in original) (quoting Twombly, 550 U.S. at 555).
“[T]he complaint must ‘state[] a plausible claim for relief’ that
‘permit[s] the court to infer more than the mere possibility of
misconduct’ based upon ‘its judicial experience and common
sense.’” Coleman v. Md. Ct. App., 626 F.3d 187, 190 (4th Cir.
2010) (alterations in original) (quoting Iqbal, 556 U.S. at 679).
As such, mere legal conclusions are not accepted as true, and
“[t]hreadbare recitals of the elements of a cause of action,
supported by mere conclusory statements, do not suffice.” Iqbal,
556 U.S. at 678.
In ruling on a Rule 12(b)(6) motion, “a court evaluates the
complaint in its entirety, as well as documents attached or
incorporated into the complaint.” E.I. du Pont de Nemours & Co.
v. Kolon Indus., Inc., 637 F.3d 435, 448 (4th Cir. 2011). The
court may also consider documents “attached to the motion to
dismiss, so long as they are integral to the complaint and
authentic.” Philips v. Pitt Cty. Mem'l Hosp., 572 F.3d 176, 180
(4th Cir. 2009). Generally, a “court cannot go beyond these
documents” without “convert[ing] the motion into one for summary
judgment,” an action from which courts should refrain “where the
parties have not had an opportunity for reasonable discovery.”
E.I. du Pont, 637 F.3d at 448.
B. Nevada Deceptive Trade Practices Act Claim
In Count I of the complaint, Plaintiff Nolan alleges that
Labcorp has violated the NDTPA. (Doc. 1. ¶¶ 153-59.) The NDTPA
authorizes an action “by any person who is a victim of consumer
fraud.” Nev. Rev. Stat. § 41.600(1). To state a claim, a plaintiff
must establish: (1) “an act of consumer fraud by the defendant,”
(2) causation, and (3) damages. Bertsch v. Discover Financial
Services, No. 2:18-cv-00290-GMN, 2020 WL 1170212, at *5 (D. Nev.
Mar. 11, 2020); Switch, Ltd. v. Uptime Inst., LLC, 426 F. Supp. 3d
636, 643 (D. Nev. 2019); Picus v. Wal-Mart Stores, Inc., 256 F.R.D.
651, 657–58 (D. Nev. 2009) (noting Nevada Supreme Court has not
specified the elements of a NDTPA claim and predicting how the
court would rule). As used in § 41.600, actionable “consumer
fraud” includes any “deceptive trade practice as defined in NRS
598.0915 to NRS 598.0925, inclusive.” Nev. Rev. Stat.
§ 41.600(2)(e); see Bertsch, 2020 WL 1170212, at *5 (D. Nev. Mar.
11, 2020).
Section 598 defines a deceptive trade practice to include:
(1) “mak[ing] false or misleading statements of fact concerning
the price of goods or services for sale or lease, or the reasons
for, existence of or amounts of price reductions” pursuant to Nev.
Rev. Stat. § 598.0915(13); (2) “knowingly mak[ing] any other false
representation in a transaction” pursuant to Nev. Rev. Stat.
§ 598.0915(15); and (3) “knowingly . . . fail[ing] to disclose a
material fact in connection with the sale or lease of goods or
services” pursuant to Nev. Rev. Stat. § 598.0923(1)(b). It is
also a deceptive trade practice when, “in the course of his or her
business”, a person “knowingly . . . [u]ses coercion, duress, or
intimidation in a transaction” pursuant to § 598.0923(1)(d), or
“knowingly . . . [u]ses an unconscionable practice in a
transaction” pursuant to § 598.0923(1)(e). Finally, the elements
of an NDTPA claim must be pleaded with particularity pursuant to
Federal Rule of Civil Procedure 9(b). Switch, 426 F. Supp. 3d at
643; see also Horner v. Mortgage Elec. Registration Sys., 711 F.
App'x 817, 818 (9th Cir. 2017). In his complaint, Nolan alleges
that Labcorp’s use of the Patient Acknowledgment and subsequent
debt collection efforts violate § 41.600 and provisions in § 598
of the NDTPA. (Doc. 1 ¶ 153-59.)
Labcorp argues that under any of these provisions Nolan’s
claims fail as a matter of law. First, it argues that Nolan cannot
state a claim under the NDTPA because “nothing in the Patient
Acknowledgment is false or misleading,” nor “is a reasonable
consumer likely to be detrimentally misled by anything it says.”
(Doc. 11 at 12-14.) Second, it argues that Nolan has failed to
“allege[] facts establishing causation” because the alleged injury
was caused by his own “apparent assumption that . . . the amount
[he] would owe would be limited to” the amount provided on the
Patient Acknowledgment. (Id. at 16-17.) And third, it argues
that Nolan’s allegations “do not meet the heightened particularity
required by Rule 9(b).” (Id. at 17.)
1. Claims Pursuant to §§ 598.0915(13) and (15)
First, Nolan contends that Labcorp’s Patient Acknowledgment
form affirmatively misleads consumers pursuant §§ 598.0915(13) and
(15). “For a plaintiff to recover based on consumer fraud under
the Deceptive Trade Practices Act, a plaintiff must . . . allege
that they reasonably relied on the alleged misrepresentation where
it is an affirmative misrepresentation rather than a failure to
disclose.” Sylver v. Exec. Jet Mgmt., Inc., No. 2:10-CV-01028,
2011 WL 9329, at *3 (D. Nev. Jan. 3, 2011) (citing Picus, 256
F.R.D. at 657–58); Heath v. Tristar Prod., Inc., No. 2:17-CV-2869-
GMN-BNW, 2019 WL 4738004, at *10 (D. Nev. Sept. 27, 2019) (“To
support a claim under the NDTPA, Plaintiff must prove that she
reasonably relied on misrepresentations or false statements made
by Defendant.”)
Here, as Labcorp correctly points out, the Patient
Acknowledgement “discloses to Plaintiffs exactly what it says it
discloses: the estimated out-of-pocket charges a patient will
incur for testing if that service is covered by the patient’s
insurance.” (Doc. 11 at 13 (emphasis in original).) Put
differently, the Patient Acknowledgment explicitly states that the
“health plan allowed rate” provides only an estimate based on the
assumption that insurance will cover the lab tests. By definition,
the “health plan allowed rate” indicates it is the most the insurer
allows the provider to charge for each enumerated test if there is
coverage. Accordingly, the average consumer who claims to have
insurance should understand as much, and Nolan could not have
reasonably relied on the Patient Acknowledgment as anything other
than an estimate of his costs if there were insurance coverage.
See Sylver, 2011 WL 9329, at *3 (dismissing NDTPA claim because
plaintiffs could not have reasonably relied on a quote to receive
a Gulfstream when the contract expressly stated that type of
chartered aircraft could change); Docena v. Navy Fed. Credit Union,
No. 3:15-CV-00184-LRH-WGC, 2016 WL 53826, at *4 (D. Nev. Jan. 4,
2016) (citation omitted) (dismissing NDTPA claim because “a
reasonable consumer would have been put on notice simply by doing
sufficient reading”); accord Freeman v. Time, Inc., 68 F.3d 285,
289 (9th Cir. 1995)(affirming dismissal of unfair competition
claim under California law because the allegedly misleading letter
clearly and inconspicuously stated the conditions plaintiff must
meet in order to qualify for the prize money).
That Nolan might not have personally read or understood the
disclosure - which he signed - is immaterial. “[A] consumer cannot
decline to read clear and easily understandable terms that are
provided on the same [page] in close proximity to the location
where the consumer indicates his agreement to those terms and then
claim that the [document], which the consumer has failed to read,
is deceptive.” Bott v. VistaPrint USA, Inc., 392 F. App'x 327,
327–28 (5th Cir. 2010) (citation omitted); Hager v. Vertrue, Inc.,
No. CIV.A. 09-11245-GAO, 2011 WL 4501046, at *6 (D. Mass. Sept.
28, 2011) (dismissing unfair competition claim under Massachusetts
law because the plaintiff, “[h]aving failed to read the materials
the defendants provided (even fairly casually),” could “not now
show the necessary connection between the allegedly deceptive
materials and her mistaken enrollment such that the defendants
would be responsible for the asserted harm.”) In Nevada, “[i]t
has long been the common law rule that signing a document
authenticates and adopts the words it contains, even if there was
a lack of subjective understanding of the words or their legal
effect.” In re Schwalb, 347 B.R. 726, 743 (Bankr. D. Nev. 2006)
(citing Campanelli v. Conservas Altamira, S.A., 477 P.2d 870, 872
(Nev. 1970)). “In essence, people are presumed to be bound by
what they sign.” Id.
Nolan also contends that by stating that a patient’s costs
“may be different,” the Patient Acknowledgment affirmatively
“misrepresents the truth in two ways.”3 (Doc. 13 at 16.) First,
Nolan argues that this statement is affirmatively misleading
because “it misrepresents the price change as being less than
certain by using the term ‘may’ instead of ‘will,’” (id.) even
though Labcorp knows that the price will be “many times higher
than the amount quoted for covered services” in the event of non-
coverage. (Doc. 13 at 16-17.) Second, Nolan argues that the
phrase “may be different than the estimated amount” misrepresents
“that the change may be higher or lower than” the health plan
allowed rate, when Labcorp knows that the amount to be charged
will be higher without insurance coverage. (Id.)
Neither of these arguments is persuasive. As Labcorp
correctly states in its reply, “[t]he sentence at issue asks
patients to acknowledge their understanding that, for a number of
stated reasons, the ultimate amount they may owe may not be the
same as – and thus ‘different’ than - the estimated insurance-
related charges.” (Doc. 15 at 4.) In other words, this sentence
simply acknowledges the “uncertainty inherent in the estimate
provided.” (Id. at 3.)
Moreover, the phrase “may be different” must be read in the
context of the Patient Acknowledgement as a whole in evaluating
whether a reasonable consumer is likely to be deceived. See
3 In relevant part, the specific sentence reads: “The amount I may have
to pay may be different than the estimated amount.” (Doc. 1-1 at 2.)
Freeman, 68 F.3d at 290 (evaluating allegedly deceptive statements
under reasonable person standard and noting that “[a]ny ambiguity
that [plaintiff] would read into any particular statement is
dispelled by the promotion as a whole”); Davis v. G.N. Mortg.
Corp., 396 F.3d 869, 884 (7th Cir. 2005) (citations omitted) (under
Illinois Consumer Fraud Act, the “allegedly deceptive act must be
looked upon in light of the totality of the information made
available to the plaintiff.”) Viewed holistically, the Patient
Acknowledgement purports to be nothing other than a conditional
estimate. Page one unambiguously states: “This estimate assumes
all services will be covered,” meaning that it is the estimate of
patient costs assuming all tests are covered by the patient’s
insurer. (See, e.g., Doc. 1-1 at 1.) This disclosure is repeated
on page two under the heading: “ACKNOWLEDGEMENT OF ESTIMATED
FINANCIAL RESPONSIBILITY.” (Id. at 2.) Page one, moreover, makes
clear that the “Health Plan Allowed Rate” is the rate the insurer
is permitted to charge, and thus the patient may owe out-of-pocket,
if the services are covered. (Id. at 1.) Thus, the “Estimated
Responsibility” noted on page two is merely the total of the
estimates provided on page one, less any deductible or co-insurance
allowance, if the insurer covers the tests. (Id.) For Nolan to
have assumed that he would be charged the “Health Plan Allowed
Rate” even if the charges were not covered by his insurance is not
a reasonable assumption based on a fair reading of the form.
Similarly, there is no reasonable basis for any inference
that the patient would ever owe anything less than the Estimated
Responsibility amount if his health insurance did not cover each
test. The form explains why certain services might not be covered
by health insurance: because, for instance, they “may be considered
investigational, require prior authorization, [or] are excluded or
otherwise not covered by your health plan.” (Id.) Additionally,
the final sentence reads, “I agree to be personally and fully
responsible for the charges from today’s services that are not
covered by my health plan.” (Id.) Thus, the totality of the
information available on the form dispels any basis for Nolan’s
claim that the form has a tendency to deceive. Accordingly,
Nolan’s allegations based on §§ 598.0915(13) and (15) fail to state
a claim on which relief may be granted.
2. Claim Pursuant to § 598.0923(1)(b)
Next, Nolan alleges that Labcorp’s “fail[ure] to disclose to
patients the patient list price that patients would be required to
pay if insurance denies coverage” (Doc. 1 ¶ 156) violates
§ 598.0923(1)(b), which makes it a deceptive trade practice to
“knowingly . . . fail[] to disclose a material fact in connection
with the sale or lease of goods or services.” In its reply brief,
Labcorp argues that because Nolan failed to allege this specific
provision of the NDTPA in the complaint (and instead merely alleges
a general violation of Chapter 598), he should be precluded from
relying on that section now. (See Doc. 15 at 5.)
Labcorp is correct that the complaint does not specifically
allege a violation of § 598.0923(1)(b). And to be sure, a
complaint may not be amended by a brief in opposition to a motion
to dismiss. See S. Walk at Broadlands Homeowner's Ass'n, Inc. v.
OpenBand at Broadlands, LLC, 713 F.3d 175, 184 (4th Cir. 2013).
This rule stems from the requirement that the “complaint . . .
give the defendant fair notice of what the claim is and the grounds
upon which it rests.” E.I. du Pont, 637 F.3d at 440. Here,
although Nolan does not specify § 598.0923(1)(b) in the complaint,
he does allege “violations of 598.0903, et seq.” (See Doc. 1 at
41.) Moreover, the complaint clearly alleges Labcorp’s “fail[ure]
to disclose to patients the patient list price” alongside the
health plan allowed rate as the primary theory of liability. (See
Doc. 1 ¶ 156; see also id. ¶¶ 3, 128.) Furthermore, the “failure
to disclose” allegations of the complaint track the text of
§ 598.0923(1)(b) itself, which makes it a deceptive trade practice
to “knowingly . . . fail to disclose” certain material facts. That
Labcorp acknowledged (and fully briefed) this self-described
“deception-by-omission theory” (Doc. 11 at 14-15), further belies
any argument that it lacked fair notice of the claim and the
grounds upon which it rested. E.I. du Pont, 637 F.3d at 440; see
also (Doc. 11 at 2) (Labcorp characterizing Nolan’s “claim” as
resting on the fact that the Patient Acknowledgment “does not
disclose the specific amount a patient might pay if their test is
not covered by his or her health plan.”) Accordingly, the
allegations were sufficient to give Labcorp notice of the provision
of the law it allegedly violated, § 598.0923(1)(b).4
Turning to the claim itself, this federal court sitting in
diversity and applying Nevada law is obliged to apply the
jurisprudence of Nevada’s highest court, the Supreme Court of
Nevada. See Private Mortg. Inv. Servs., Inc. v. Hotel & Club
Assocs., Inc., 296 F.3d 308, 312 (4th Cir. 2002). When that court
has not spoken directly on an issue, this court must “predict how
that court would rule if presented with the issue.” Id. The
decisions of the Nevada Court of Appeals are the “next best
indicia” of what Nevada’s law is, though its decisions “may be
disregarded if the federal court is convinced by other persuasive
data that the highest court of the state would decide otherwise.”
Id. (quoting Liberty Mut. Ins. Co. v. Triangle Indus., Inc., 957
F.2d 1153, 1156 (4th Cir. 1992)). In predicting how the highest
court of a state would address an issue, however, this court
4 Alternatively, because this alleged deficiency is easily correctible
by amendment, the parties have briefed the issue, and to conserve
judicial and party resources, the court would reach the same conclusion
and exercise its discretion to determine whether the complaint states a
claim under § 598.0923(1)(b). See Poindexter v. Stuteville, No. CIV-
12-0031-F, 2012 WL 13035041, at *4 (W.D. Okla. May 10, 2012) (electing
to address whether the allegations stated a claim under § 1962(c) despite
complaint’s failure to specify which subsection of § 1962 defendant
allegedly violated because the issue was fully briefed and deciding it
would conserve resources).
“should not create or expand a [s]tate's public policy.” Time
Warner Entm't-Advance/Newhouse P'ship v. Carteret-Craven Elec.
Membership Corp., 506 F.3d 304, 314 (4th Cir. 2007) (alteration
and quotation omitted). Moreover, “absent a strong countervailing
federal interest,” a federal court should not interject itself
into a controversy to render what may be an “uncertain and
ephemeral interpretation of state law.” Id.; see Burris Chem.,
Inc. v. USX Corp., 10 F.3d 243, 247 (4th Cir. 1993) (noting that
federal courts adjudicating issues of state law “rule upon state
law as it exists and do not surmise or suggest its expansion”).
Here, the parties have not identified a case to support a
duty to disclose price to a customer under Nevada law. Labcorp
cites Mallory v. McCarthy & Holthus, LLP, No. 2:14-CV-00396-KJD,
2015 WL 2185413, at *3 (D. Nev. May 11, 2015), which dismissed
NDTPA claims because plaintiff did “not identify how Defendant is
bound, under Nevada law, to disclose the information” allegedly
omitted. However, those claims were brought under § 598.0915(15),
which addresses affirmative representations. A similar result
appears in MST Management, LLC v. Chicago Doughnut Franchise Co.,
LLC, 584 F. Supp. 3d 923, 933 (D. Nev. 2022), which dismissed NDTPA
claims based on “alleged omissions” on the grounds that the
plaintiff failed to identify or argue the existence of a duty to
disclose under “the DTPA, other state law, or the contracts between
the parties,” but permitted plaintiffs’ affirmative
misrepresentation claims to proceed. While not apparent in the
court’s opinion, the parties’ briefs indicate that the plaintiffs’
claims were brought pursuant to §§ 598.0915(5), (7), and (15),
which all address affirmative representations. These cases are
therefore not on point.
Nolan relies heavily on Poole v. Nevada Auto Dealership
Investments, LLC, 449 P.3d 479 (Nev. App. 2019). In Poole, the
plaintiff purchased a certified pre-owned truck from the
defendant-dealer. Id. at 481. Before purchasing the truck, the
plaintiff asked about the truck's accident history and was told it
had been in a “minor” accident. Id. He was also told that the
defendant “would not sell the truck were the collision
significant.” Id. Two years later, when attempting to refinance
the truck loan, the plaintiff learned that the truck had in fact
been in a major accident resulting in significant damage, thereby
“significantly” affecting the value of the truck. Id. at 481-82.
The plaintiff sued for “failing to disclose a material fact” under
§ 598.0923(2) of the NDTPA, the substantively identical
predecessor to § 598.0923(1)(b). On appeal, the Nevada Court of
Appeals held that the plaintiff had presented sufficient evidence
to create a factual dispute and reversed the lower court’s grant
of summary judgment. Id. at 490-91.
While the court of appeals analyzed Poole’s claim under the
rubric of nondisclosure, see id. at 488 (characterizing
defendant’s failure as not disclosing “the extent of the damage”
to the car), plaintiff’s claim clearly rested on the defendant’s
prior affirmative misrepresentation. As the Nevada Court of
Appeals recounted, plaintiff’s evidence (viewed in the light most
favorable to him at the summary judgment stage) established that
the defendant auto-dealer affirmatively misled the plaintiff about
the truck’s condition when its employee lied to him: when asked
about the car’s previous collision, the salesperson “assured
[Poole] that the collision was only minor,” when in fact that
salesperson knew that the prior collision “had damaged the truck’s
frame and significantly reduced its value.” Id. at 481. Poole is
therefore distinguishable, as its holding relied on an affirmative
misrepresentation.
The court’s own analysis reveals one federal case
interpreting Nevada law that denied a motion to dismiss a claim
under § 598.0923(1)(b) where the defendant argued that the statute
requires an affirmative duty to disclose. In Smallman v. MGM
Resorts International, No. 220CV00376GMNEJY, 2022 WL 16636958, at
*12 (D. Nev. Nov. 2, 2022), plaintiffs brought a claim under
§ 598.0923(1)(b) against the defendant hotel alleging a failure to
disclose its allegedly deficient data security practices and
likelihood of being a frequent target of sophisticated
cyberattacks. The federal court distinguished another Nevada
district court decision, Soffer v. Five Mile Capital Partners,
LLC, No. 12-CV-1407, 2013 WL 638832, at *10 (D. Nev. Feb. 19,
2013), cited by the defendant, which observed that, under Nevada
law, common law fraud by omission requires an affirmative duty to
disclose. Id.5 The Smallman court also noted the Nevada Supreme
Court’s general statement that “[s]tatutory offenses that sound in
fraud are separate and distinct from common law fraud.” Id.
(quoting Leigh-Pink v. Rio Properties, LLC, 512 P.3d 322, 328 (Nev.
2022)).6 Based on these two observations, the Smallman court
concluded that the defendant “has not shown that fraud by omission
5 See, e.g., Dow Chem. Co. v. Mahlum, 970 P.2d 98, 110 (Nev. 1998) (common
law fraud requires duty to disclose), abrogated on other grounds by GES,
Inc., v. Corbitt, 21 P.3d 11 (Nev. 2001). Nevada’s common law on duty
to disclose in omission cases is consistent with the law of other
jurisdictions. See, e.g., Chiarella v. United States, 445 U.S. 222, 228
(1980) (noting that at common law, fraud doctrine did not impose a duty
to disclose in the absence of a fiduciary or other similar relation of
trust and confidence); Eller v. EquiTrust Life Ins. Co., 778 F.3d 1089,
1092 (9th Cir. 2015) (noting “the settled premise that a seller generally
has no duty to disclose internal pricing policies or its method for
valuing what it sells”); Langford v. Rite Aid of Alabama, Inc., 231 F.3d
1308, 1313–14 (11th Cir. 2000) (rejecting claim that federal law obliges
retailers to disclose pricing structure to consumers); Bonilla v. Volvo
Car Corp., 150 F.3d 62, 71 (1st Cir. 1998) (also finding that federal
law imposes no obligation on retailers to disclose their pricing
structure to consumers, and rejecting fraud claim based on contention
that car buyers would not have paid for accessories had they known the
seller’s mark-up was so high and the accessories so minor).
6 Leigh-Pink involved a damages question, not a duty to disclose. The
Nevada Supreme Court went on to state that “statutes should be
interpreted consistently with the common law,” and noted that its
interpretation of Nev. Rev. Stat. § 41.600(3) in that case had the
“salutary purpose of coupling the statutory consumer fraud understanding
of damages with this court’s determination of damages at common law.”
512 P.3d at 328 (quoting in part Samantar v. Yousuf, 560 U.S. 305, 320
(2010)). The Leigh-Pink court concluded that while the NDTPA should be
construed liberally to accord with its remedial purposes, “such a liberal
construction must be faithful to the first principles of statutory
interpretation” requiring application of the plain language of the
statute “in accord with the term’s definition at common law.” Id.
under NRS § 598.0923(1)(b) requires an affirmative duty to
disclose.” Id.
Other states with similar, but perhaps not identical,
statutes differ as to whether a duty to disclose is required for
a statutory omission claim. For example, Arizona courts are split
on whether a duty to disclose is required. Compare Tavilla v.
Cephalon, Inc., 870 F. Supp. 2d 759, 776 (D. Ariz. 2012) (citations
omitted) (“Generally stated, claims under the [Arizona Consumer
Fraud Act], like common law fraud claims, can be based on . .
. omission of material facts,” but “[t]o the extent that
‘omission’ suggests that mere silence as to material facts may be
actionable without a duty to disclose, the Arizona Court of Appeals
has rejected this interpretation.”) and Loomis v. U.S. Bank Home
Mortg., 912 F. Supp. 2d 848, 857 (D. Ariz. 2012) (same); with
Cheatham v. ADT Corp., 161 F. Supp. 3d 815, 830 (D. Ariz. 2016)
(arguing that Loomis “misapprehended Arizona law” and ignored the
Arizona Supreme Court’s decision in State ex rel. Horne v.
AutoZone, Inc., 275 P.3d 1278, 1281 (Ariz. 2012)).7 Michigan
7 Ariz. Rev. Stat. Ann. § 44-1522 provides:
The act, use or employment by any person of any deception,
deceptive or unfair act or practice, fraud, false pretense,
false promise, misrepresentation, or concealment, suppression
or omission of any material fact with intent that others rely
on such concealment, suppression or omission, in connection
with the sale or advertisement of any merchandise whether or
not any person has in fact been misled, deceived or damaged
thereby, is declared to be an unlawful practice.
courts appear to require a duty to disclose. See, e.g., Hendricks
v. DSW Shoe Warehouse Inc., 444 F. Supp. 2d 775, 782 (W.D. Mich.
2006) (interpreting the Michigan Consumer Protection Act, which
proscribes “[f]ailing to reveal a material fact, the omission of
which tends to mislead or deceive the consumer,” and concluding
that Michigan courts would not recognize a claim under this
provision for an omission “in the absence of a duty of
disclosure”).8 Kansas courts similarly appear to require a duty
to disclose. See, e.g., Williamson v. Amrani, 152 P.3d 60, 73
(Kan. 2007) (concluding that in order for failure to disclose a
material fact to constitute a deceptive act under the Kansas
Consumer Protection Act,9 “there must be a duty to disclose the
fact”), superseded by statute on other grounds, Kan. Stat. Ann.
§ 50-635(b), as recognized in Kelly v. VinZant, 197 P.3d 803, 811
(Kan. 2008); Nieberding v. Barrette Outdoor Living, Inc., 302
F.R.D. 600, 614 (D. Kan. 2014) (“To make a willful omission claim
under § 50-626(b)(3)” the “[p]laintiff also must show that
defendants had a duty to disclose the material fact.”). New
8 The Michigan Consumer Protection Act, Mich. Comp. Laws Ann. § 445.903,
defines unfair or deceptive acts to include “[f]ailing to reveal a
material fact, the omission of which tends to mislead or deceive the
consumer, and which fact could not be known by the consumer.”
9 Kan. Stat. Ann. § 50–626(b)(3) defines deceptive acts and practices to
include “the willful failure to state a material fact, or the willful
concealment, suppression or omission of a material fact.”
Mexico, by contrast, may not require an independent duty to
disclose. See, e.g., Smoot v. Physicians Life Ins. Co., 87 P.3d
545, 549 (N.M. Ct. App. 2003) (holding that N.M. Stat. Ann. § 57-
12-2(D)(14) “imposes a duty to disclose material facts reasonably
necessary to prevent any statements from being misleading”).10
Based on the limited authority provided, it is not clear how
the Nevada Supreme Court would interpret the duty to disclose in
the present case, where an accurate estimated price was in fact
disclosed based on a representation and assumption that the
patient/customer had insurance coverage. Even assuming
§ 598.0923(1)(b) imposes a duty to disclose of some form, however,
this federal court sitting in the Middle District of North Carolina
declines to presume that the Nevada Supreme Court would extend the
statute to the claim in this case. Time Warner Ent.-
Advance/Newhouse P'ship, 506 F.3d at 314 (noting federal court
sitting in diversity should not “elbow its way” into a controversy
that might create or expand a state’s public policy); see Bauer v.
Charter Sch. USA, Inc., No. 5:21-CV-492-FL, 2022 WL 2721339, at *3
(E.D.N.C. July 13, 2022) (same). Nolan’s claim is predicated on
his representations to Labcorp that he had insurance for his
testing and the identity of his insurer. The Patient
10 N.M. Stat. Ann. § 57-12-2(D)(14) includes within its definition of
unfair trade practices “failing to state a material fact if doing so
deceives or intends to deceive.”
Acknowledgement is a response to that request, and thus discloses
the estimated prices he may be charged should his representations
be correct and should the tests be covered by his insurance -
contingencies that are disclosed in the Patient Acknowledgement.
Nolan does not allege that the estimated prices are misleading if
the tests are in fact covered by his insurance; put differently,
there is no allegation that Labcorp failed to disclose the proper
price based on Nolan’s representations. Nowhere does Labcorp
represent that the tests will in fact be covered, nor does Nolan
represent that Labcorp knows that the test will not be covered.
Other prices could apply depending on, among other factors, how
much the insurance company later deems covered and what insurance
benefits the patient has purchased (including whether the service
is in-network). To hold that under these circumstances - where a
customer/patient represents he has insurance - a provider must
disclose the possible list price would, by implication, subject
the provider to liability for not disclosing all other possible
prices and impose a heavy burden on service providers that it would
seem the law has heretofore not contemplated.11 Accordingly,
11 It is well-established, for instance, that in the context of providing
for health care services “precision concerning price is close to
impossible.” Allen v. Clarian Health Partners, Inc., 980 N.E.2d 306,
310 (Ind. 2012); see Nygaard v. Sioux Valley Hosps. & Health Sys., 731
N.W.2d 184, 193 (N.D. 2007) (noting that “in a hospital setting, it is
not possible to know at the outset what the cost of the treatment will
be”); Shelton v. Duke Univ. Health Sys., Inc., 633 S.E.2d 113, 116 (N.C.
Ct. App. 2006) (“Inherent in providing medical care and treatment is the
Nolan’s reliance on § 598.0923(1)(b) is unavailing.
3. Claims Pursuant to §§ 598.0923(1)(d) and (e)
Nolan next claims that Labcorp’s debt collection practices
were coercive in violation of Nev. Rev. Stat. § 598.0923(1)(d).
He concedes that it is not “inherently coercive” to report unpaid
debts to credit bureaus or collection agencies. (Doc. 13 at 18.)
He argues, however, that Labcorp’s practice of using “non-physical
threats to compel compliance with its wrongful demand that he pay
its inflated PLP for the Vitamin D test” violated the statute.
(Id.) Labcorp responds that Nolan has failed to plead a claim
under § 598.0923(1)(d) in the complaint and raised this claim for
the first time in his response brief. (Doc. 15 at 9-12.) Labcorp
also argues that it cannot be coercive or wrongful to seek
collection of the list price. (Id. at 12.)
The statute provides that a person engages in a deceptive
trade practice when “in the course of his or her business he or
element of the unforeseen.”). For this reason, courts have routinely
rejected the argument that healthcare contracts that fail to specify
price upfront are unenforceable. See DiCarlo v. St. Mary Hosp., 530
F.3d 255, 264 (3d Cir. 2008)(“Besides handing the patient an inches-high
stack of papers detailing the hospital's charges for each and every
conceivable service, which he or she could not possibly read and
understand before agreeing to treatment, the form contract [explaining
that the price term is “all charges”] employed by [defendant] is the
only way to communicate to a patient the nature of his or her financial
obligations to the hospital.”); Allen, 908 N.E.2d at 309-311 (collecting
cases); Pitell v. King Cnty. Pub. Hosp. Dist. No. 2, 423 P.3d 900, 902
(Wash. Ct. App. 2018) (collecting cases); Mark A. Hall and Carl E.
Schneider, Patients as Consumers: Courts, Contracts, and the New Medical
Marketplace, 106 Mich. L. Rev. 643, 674 (2008) (explaining that “courts
have generally tolerated low levels of specificity in medical
contracts”).
she knowingly . . . [u]ses coercion, duress or intimidation in a
transaction.” Nev. Rev. Stat. § 598.0923(1)(d). It is true that
while the complaint contained allegations referencing Labcorp’s
collection efforts, Nolan’s articulation of this claim arose for
the first time in his response brief; Count I of the complaint
contains no reference to any specific alleged statutory violation.
As one federal district court in Nevada has explained, “[m]erely
alleging a general violation of Chapter 598 is insufficient to
give the defendants notice of the prohibited conduct they engaged
in or the provisions they allegedly violated.” Laforge v. Richland
Holdings, Inc., No. 2:17-CV-00782, 2018 WL 525298, at *8 (D. Nev.
Jan. 23, 2018) (noting that “Chapter 598 contains ten sections,
each defining a separate set of deceptive practices,” and “[e]ach
of those sections further enumerates categories of conduct, some
identifying as many as 16 sub-categories of prohibited acts”); see
Austin v. Allied Collection Servs., Inc., No. 221CV01593CDSNJK,
2023 WL 375988, at *5 (D. Nev. Jan. 23, 2023) (“But plaintiff is
required to, at the very least, cite which specific subsections of
the [NDTPA] she accuses the defendants of violating, to place the
defendants on notice.”) Nolan’s claim was therefore not properly
pleaded.
Nolan also raises an unconscionability claim pursuant to
§ 598.0923(1)(e). The court finds that this pleading was
defective. In his response brief, Nolan attempts to supplement
the allegations of the complaint by claiming that Labcorp’s
“actions after October 21, 2021, constitute the use of ‘an
unconscionable practice in a transaction.’” (Doc. 13 at 19
(quoting Nev. Rev. Stat. 598.0923(1)(e)). The complaint, however,
does not include any allegation involving conduct after October
2021. This is unsurprising, as that section of the statute was
not added by amendment until October 1, 2021, and therefore Labcorp
could not have violated it as to Nolan’s September 2018 interaction
with Labcorp. See Nev. Rev. Stat. Ann. § 598.0923 (West 2021)
(effective date October 1, 2021). Nolan argues, nevertheless and
in conclusory fashion, that the Patient Acknowledgement is
“unconscionable” because it facilitates Labcorp’s practice of
charging patients for tests at prices that grossly exceed their
market value. (Id.) A “proffered argument is not a pleaded
factual allegation.” Mack v. E. Carolina Univ., No. 4:21-CV-
00108-M, 2022 WL 945595, at *6 (E.D.N.C. Mar. 29, 2022). For these
reasons, the court will not consider Nolan’s contention that
Labcorp has violated § 598.0923(1)(e) as to him. See Car Carriers,
Inc. v. Ford Motor Co., 745 F.2d 1101, 1107 (7th Cir. 1984) (“[I]t
is axiomatic that the complaint may not be amended by the briefs
in opposition to a motion to dismiss”). Accordingly, to the extent
Nolan contends he has such a claim, it will be dismissed without
prejudice.
4. Conclusion
In sum, Nolan’s complaint does not contain factual
allegations to support a plausible claim that Labcorp engaged in
a deceptive trade practice under the NDTPA. Accordingly, Count I
will be dismissed for failure to state a claim upon which relief
can be granted, except for Nolan’s argued claims based on
§§ 598.0923(1)(d) and (e), which will be dismissed without
prejudice.
C. Florida Deceptive and Unfair Trade Practices Act Claim
Pursuant to the FDUTPA, “[u]nfair methods of competition,
unconscionable acts or practices, and unfair or deceptive acts or
practices in the conduct of any trade or commerce are ...
unlawful.” Fla. Stat. § 501.204(1). The three elements of a
consumer claim under the FDUTPA are: “(1) a deceptive act or unfair
practice; (2) causation; and (3) actual damages.” Marrache v.
Bacardi U.S.A., Inc., 17 F.4th 1084, 1097–98 (11th Cir. 2021); see
also City First Mortg. Corp. v. Barton, 988 So. 2d 82, 86 (Fla.
Dist. Ct. App. 2008).
A deceptive act “occurs if there is a representation,
omission, or practice that is likely to mislead the consumer acting
reasonably in the circumstances, to the consumer's detriment.”
PNR, Inc. v. Beacon Prop. Mgmt., Inc., 842 So.2d 773, 777 (Fla.
2003) (citation and internal quotation marks omitted). “An
objective test is used to determine whether an act is deceptive
under FDUTPA, and ‘the plaintiff must show that the alleged
practice was likely to deceive a consumer acting reasonably in the
same circumstances.’” Marrache, 17 F.4th at 1098 (quoting
Carriuolo v. Gen. Motors Co., 823 F.3d 977, 985–86 (11th Cir.
2016)). To establish an unfair practice, “the plaintiff must show
that it is ‘one that offends established public policy and one
that is immoral, unethical, oppressive, unscrupulous or
substantially injurious to consumers.’” Marrache, 17 F.4th at
1098 (quoting PNR, 842 So. 2d at 777). Whether the alleged facts
constitute a deceptive or unfair act is a question of law for the
court. See PNR, 842 So. 2d at 777 n.2 (stating that the relevant
question is whether plaintiff pleaded conduct that is “unfair or
deceptive as judged by controlling case law”); Casey v. Fla.
Coastal Sch. of L., Inc., No. 3:14-CV-1229-J-39PDB, 2015 WL
10096084, at *6 (M.D. Fla. Aug. 11, 2015), report and
recommendation adopted, No. 3:14-CV-01229, 2015 WL 10818746 (M.D.
Fla. Sept. 29, 2015) (“Whether an alleged act or practice is
deceptive or unfair may be decided as a matter of law”); Zambrano
v. Indian Creek Holding, LLC, No. 09-20453-CIV, 2009 WL 2365842,
at *1 (S.D. Fla. July 30, 2009) (same).12
12 Though neither party discusses them in their briefing, a few cases
contain language to the effect that whether an act is unfair or deceptive
is “generally” a question of fact. See, e.g., Gov't Emps. Ins. Co. v.
Glassco Inc., No. 8:19-CV-1950-KKM-JSS, 2021 WL 4391717, at *16 (M.D.
Fla. Sept. 24, 2021) (citing Suris v. Gilmore Liquidating, Inc., 651 So.
2d 1282, 1283 (Fla. Dist. Ct. App. 1995)); Siever v. BWGaskets, Inc.,
Plaintiff Wittenberg alleges that Labcorp’s use of the
Patient Acknowledgment is both deceptive and unfair. (Doc. 1
¶¶ 162-63.) In support of these claims, she argues that despite
its plain language, the Patient Acknowledgment is nonetheless
deceptive and unfair under the FDUTPA because Labcorp “knows and
fails to disclose that the amount it bills patients if insurance
does not cover the test is many multiples [more] than the disclosed
amount.” (Doc. 1 ¶ 3, 163; Doc. 13 at 25-26.) In other words,
Wittenberg’s theory is one of deception by omission: that Labcorp’s
failure to disclose the patient list price in conjunction with the
health plan allowed rate constituted a deceptive act or unfair
practice under Florida law.13 (Doc. 1 ¶¶ 114-15, 163; Doc. 13 at
18.)
It is unclear whether Wittenberg must establish an
independent duty to disclose on a FDUTPA claim based on an omission
669 F. Supp. 2d 1286, 1293 (M.D. Fla. 2009)) (same). A close reading
of Suris, on which these cases rely, clarifies this inference. In Suris,
the court reversed a directed verdict for the auto-dealer defendant
because the conduct alleged, if believed by a jury, could constitute a
FDUTPA claim. In other words, the court found that there was a factual
question as to whether the alleged conduct occurred, not whether the
conduct constituted an unfair and deceptive practice. Moreover, any
inference that the question of whether conduct falls under the FDUTPA
is a question of fact is dispelled by the Florida Supreme Court’s
observation that the FDUTPA “only reaches conduct that is unfair or
deceptive as judged by controlling case law.” PNR, 842 So. 2d at 777
n.2.
13 As noted, deception under the FDUTPA may be accomplished through
omissions “rather than outright false statements.” See Millennium
Commc'ns & Fulfillment, Inc. v. Office of Attorney Gen., Dep't of Legal
Affairs, State of Fla., 761 So.2d 1256, 1264 (Fla. Dist. Ct. App. 2000).
affirmatively used to mislead. See Virgilio v. Ryland Group, Inc.,
680 F.3d 1329, 1337-38 (11th Cir. 2012) (declining to decide
“whether or not a duty to disclose is an element of a FDUTPA claim”
based on an omission); Coffey v. WCW & Air, Inc., No. 3:17-CV-90-
MCR-CJK, 2018 WL 4154256, at *4 (N.D. Fla. Aug. 30, 2018) (noting
that it is undecided whether a duty to disclose is an element of
a FDUTPA claim based on an omission); compare Morris v. ADT Sec.
Servs., 580 F. Supp. 2d 1305, 1310 (S.D. Fla. 2008) (holding that
“a duty to disclose is not an element of FDUTPA”); with Parziale
v. HP, Inc., 445 F. Supp. 3d 435, 444 (N.D. Cal. 2020) (holding
the opposite).
However, even assuming a duty to disclose is not an element
of an FDUTPA claim based on an omission, Wittenberg has failed to
plausibly allege that the Patient Acknowledgment - taken as a whole
- “was likely to deceive a consumer acting reasonably in the same
circumstances.” Carriuolo, 823 F.3d at 983–84 (quoting State,
Office of the Att'y Gen. v. Commerce Comm. Leasing, LLC, 946 So.2d
1253, 1258 (Fla. Dist. Ct. App. 2007)). As noted in connection
with Nolan’s claim, by its terms the Patient Acknowledgement
provides an estimate of the rate charged “assum[ing] all services
will be covered” by the patient’s insurer. (Doc. 1-2 at 2.) There
are no assurances that health insurance will cover the tests, and
there are no assurances the estimate will be the ultimate amount
for which the patient is financially responsible. (Id.) To the
contrary, the Patient Acknowledgment explains that “the amount
[you] may have to pay may be different than the estimated amount.”
(Doc. 1-1 at 2; Doc. 1-2 at 2; Doc. 1-3 at 2), and it details why
certain services might not be covered by health insurance - they
“may be considered investigational, require prior authorization,
are excluded or otherwise not covered by your health plan.” (Id.)
By signing the Patient Acknowledgment, moreover, each patient
agrees “to be personally and fully responsible for charges from
today’s services that are not covered by your health plan.” (Id.)
This qualifying language is neither hidden nor unreadable; rather,
it appears immediately above the signature line that Wittenberg
was required to sign before she submitted to her lab tests. (Id.)
In light of these provisions, no reasonable consumer would
believe that the Patient Acknowledgement provided anything other
than a price estimate based on the assumption, presented by
Wittenberg, that she had health insurance, and that her health
insurance would cover each test. See Zlotnick v. Premier Sales
Grp., Inc., 480 F.3d 1281, 1285 (11th Cir. 2007) (holding that the
plaintiff failed to properly allege the elements of a FDUTPA claim
where the “express terms of the reservation agreement” undermined
the claim that the agreement was deceptive); Piescik v. CVS
Pharmacy, Inc., 576 F. Supp. 3d 1125, 1133 (S.D. Fla. 2021)
(dismissing FDUTPA claim for “fail[ing] to plead a deceptive act”
because a “reasonable consumer would not be expected to ignore”
the “accurate information” disclosed on the label); St. Francis
Holdings, LLC v. Pawnee Leasing Corp., No. 8:20-CV-1101-T-02, 2020
WL 6287684, at *6 (M.D. Fla. Oct. 27, 2020)(holding that the
defendant’s actions did “not amount to a deceptive or unfair trade
practice [pursuant to FDUTPA] because the terms of the agreement
were clear and Plaintiffs . . . voluntarily agreed to them”).
It is true that the Patient Acknowledgment does not disclose
the patient list price, or that the patient list price would likely
be higher than the health plan allowed rate. But the explicit
disclaimer that the amount due “may be different than the estimated
amount,” along with the admonition that the patient would be
“personally and fully responsible for charges from today’s
services that are not covered by your health plan,” is more than
sufficient to counter any potential misconception about the health
plan allowed rate disclosed on page one of the Patient
Acknowledgment. See Zlotnick, 480 F.3d at 1284 (holding that the
relevant standard “requires a showing of probable, not possible,
deception.”) For Wittenberg to now claim the Patient
Acknowledgement led her astray is unavailing, and she cannot
“reasonably claim that such clear and unambiguous statements were
deceiving.” Beale v. Biomet, Inc., 492 F. Supp. 2d 1360, 1374
(S.D. Fla. 2007). Accordingly, Wittenberg has not alleged
sufficient facts showing that Labcorp’s Patient Acknowledgement is
“likely to cause injury to a reasonable relying consumer,”
Zlotnick, 480 F.3d at 1284 (quoting Millennium Commc'ns &
Fulfillment, Inc. v. Office of the Att'y Gen., 761 So.2d 1256,
1263 (Fla. Dist. Ct. App. 2000)), and therefore has not plausibly
alleged the existence of a “deceptive act” under the FDUTPA.
Wittenberg’s contrary arguments are unconvincing.
Wittenberg primarily relies on State Farm Mut. Auto. Ins. Co. v.
At Home Auto Glass LLC, No. 8:21-CV-239-TPB-AEP, 2021 WL 6118102,
*1 (M.D. Fla. Dec. 27, 2021), which she contends establishes that
“[a]n allegation of ‘charging inflated prices not disclosed to the
customer’ is sufficient to state a claim under the Florida Act.”
(Doc. 13 at 17, 20 (quoting State Farm, 2021 WL 6118102 at *5).)
This reading of State Farm, however, is out of context. There,
unlike here, the defendant’s alleged practice of charging
customer’s undisclosed amounts resulted from a deliberate and
“orchestrated scheme” of affirmative acts which included
“falsifying information [in] its application to register as a
repair shop, concealing information about its business operations,
failing to provide customers with written estimates,
misrepresenting the nature of the repair charges and the hours
spent on repairs, and falsely telling the customer that the repairs
would be free or at no cost to them.” State Farm, 2021 WL 6118102
at *1, *6. Suffice it to say that no such allegations are made
here.
Wittenberg’s citation to Department of Legal Affairs v.
Father & Son Moving & Storage, Incorporated, 643 So.2d 22 (Fla.
Dist. Ct. App. 1994), is similarly unpersuasive. There, the
Florida District Court of Appeals simply held that a whether a
defendant violated a “specific rule or regulation is not necessary
to the determination of what constitutes an unfair or deceptive
practice” under the FDUTPA. (Id. at 24.) The court remanded the
case to the trial court to determine whether the defendant’s
actions could nevertheless constitute an unfair and deceptive
trade practice in the absence of an “administrative rule or
regulation specifying that the conduct of [the defendant] was
prohibited.” (Id. at 26.) In other words, the case merely
establishes that a plaintiff need not prove that a defendant
violated a statute or rule to state a claim under the FDUTPA.
Thus, contrary to Plaintiff’s assertions, Father & Son Moving fails
to establish that “Labcorp’s actions are similar to those that
have previously been held sufficient to state a claim under the
Florida Act.” (Doc. 13 at 17.)
Wittenberg has also failed to allege sufficient facts showing
that Labcorp’s use of the Patient Acknowledgment constitutes an
“unfair practice.” See PNR, 842 So. 2d 773, 777 (Fla. 2003)
(stating that under the FDUTPA, an unfair practice is “one that
offends established public policy and one that is immoral,
unethical, oppressive, unscrupulous or substantially injurious to
consumers.”) Nowhere does Wittenberg explain how the Patient
Acknowledgment violates established public policy. See Warren
Tech., Inc. v. UL LLC, No. 1:18-CV-21019-UU, 2018 WL 10550930, at
*11 (S.D. Fla. Oct. 31, 2018), aff'd, 962 F.3d 1324 (11th Cir.
2020) (dismissing FDUTPA claim where plaintiffs failed to explain
how defendant had violated established public policy). Nor has
Wittenberg alleged facts showing that Labcorp violated her rights
in an immoral, deceitful, or unscrupulous way. See Casa Dimitri
Corp. v. Invicta Watch Co. of Am., Inc., 270 F. Supp. 3d 1340,
1353 (S.D. Fla. 2017) (dismissing FDUTPA claim on this ground).
As with Nolan’s claim, Wittenberg’s claim is predicated on her
representations to Labcorp that she has insurance for her testing
and the name of the insurer. The Patient Acknowledgement
accurately discloses the estimated prices she may be charged should
her representations be correct and if the tests are covered by her
insurance. Wittenberg does not allege that the estimated prices
are incorrect if the tests are in fact covered by his insurance.
In this respect, Labcorp disclosed the proper price based on the
representations made by Wittenberg. Thus, Wittenberg has also
failed to plausibly allege the existence of an “unfair practice.”
For these reasons, Wittenberg has failed to state a claim
under the FDUTPA. Count II will therefore be dismissed with
prejudice.
III. CONCLUSION
For the reasons set forth above,
IT IS ORDERED that Defendant’s motion to dismiss (Doc. 10) is
GRANTED and that all claims are DISMISSED WITH PREJUDICE except
for those by Plaintiff Nolan based on alleged violations of Nev.
Rev. Stat. §§ 598.0923(1)(d) and (e), which are DISMISSED WITHOUT
PREJUDICE.
/s/ Thomas D. Schroeder
United States District Judge
February 13, 2023