Carl Thulin v. Shopko Stores Operating Co., L , 771 F.3d 994 ( 2014 )


Menu:
  •                                 In the
    United States Court of Appeals
    For the Seventh Circuit
    ________________________
    No. 13-3638
    CARL E. THULIN,
    Plaintiff-Appellant,
    v.
    SHOPKO STORES OPERATING CO., LLC,
    Defendant-Appellee.
    __________________________
    Appeal from the United States District Court for the
    Western District of Wisconsin
    No. 3:10-cv-00196 – William M. Conley, Judge
    __________________________
    ARGUED APRIL 25, 2014—DECIDED NOVEMBER 12, 2014
    __________________________
    Before KANNE and ROVNER, Circuit Judges, and DOW,
    District Judge. ∗
    DOW, District Judge. Relator Carl E. Thulin worked as a
    pharmacist at a Shopko retail store in Idaho from 2006 to
    2009. During his tenure, Thulin observed what he believed
    ∗
    The Honorable Robert M. Dow, Jr., of the Northern District of Illinois,
    sitting by designation.
    2                                               No. 13-3638
    to be a fraudulent billing scheme in which Shopko submitted
    inflated claims for prescription drugs to the federal
    Medicaid program. Thulin filed a qui tam complaint against
    his former employer in its home state of Wisconsin, alleging
    that Shopko violated the federal False Claims Act by
    overbilling Medicaid. Thulin also asserted analogous claims
    under the laws of eight different states in which Shopko
    does business. Shopko moved to dismiss Thulin’s federal
    claim under Federal Rules of Civil Procedure 9(b) and
    12(b)(6). The district court granted the motion and declined
    to exercise supplemental jurisdiction over Thulin’s state law
    claims. Finding no error, we affirm.
    I.
    Because this appeal comes to us from the grant of a
    motion to dismiss, we accept all facts alleged in Thulin’s
    complaint as true and draw all reasonable inferences in his
    favor. Shopko is a multi-regional retail pharmacy
    corporation headquartered in Green Bay, Wisconsin, that
    operates nearly 300 stores in 24 states. Thulin is a licensed
    pharmacist who at all relevant times worked as a full-time
    pharmacist at a Shopko retail store in Idaho.
    Some of Shopko’s pharmacy customers have prescription
    coverage through both private insurance and Medicaid, a
    federal program administered by the states that provides the
    poor, disabled, and elderly with medical and pharmaceutical
    insurance coverage. We follow the parties’ convention of
    referring to these individuals as “dual-eligibles.” For dual-
    eligibles, Medicaid acts as a “payer of last resort,” which
    means that it picks up any tab remaining after the dual-
    No. 13-3638                                                  3
    eligible’s private insurer has paid the amount that it has
    contracted to pay Shopko for a particular prescription.
    According to Thulin, an excess tab almost always exists.
    Both Medicaid and private insurers strive to negotiate
    pharmaceutical discounts and purchasing agreements for
    their members, but Thulin asserts that private insurers are
    much better at playing ball than are the government
    agencies administering Medicaid. The private insurers’
    negotiating prowess “results in better pricing of
    prescriptions for the [privately] insured patients.” Thulin
    alleges that this disparity exists in all of the states in which
    Shopko does business. Thus, when Shopko enters into
    provider contracts with private insurers, it typically agrees
    to accept payment in full lesser amounts than it agrees to
    accept from Medicaid for any given drug. The amount that
    Shopko agrees to accept is composed of some payment by
    the insurance company and a co-pay or deductible paid by
    the patient at the point of sale. The size of the patient’s co-
    pay depends on his or her contract with the private
    insurance company, to which Shopko is not a party.
    Privately insured patients, including dual-eligibles, are not
    parties to the contracts that Shopko signs with their private
    insurers.
    Thulin alleges that when dual-eligibles apply for
    Medicaid, they are required by 42 U.S.C. § 1396k(a)(1)(A)
    and 
    42 C.F.R. § 433.145
     to assign to the state any rights they
    have under their private insurance plans. Thulin alleges that
    one of these assignable rights is the right to purchase
    prescription drugs at the lower price that their private
    insurer negotiated with Shopko. Because dual-eligibles are
    not parties to the contracts that Shopko signs with their
    private insurers, however, they do “not know the price they
    4                                                No. 13-3638
    have legally assigned to the state Medicaid agency.”
    Likewise, Thulin alleges, state Medicaid agencies “do not
    know the price benefit that the dual-eligible patient assigns
    to the government.” In other words, both Medicaid agencies
    and dual-eligibles rely on Shopko to accurately calculate and
    assign the benefits to the government.
    According to Thulin, this reliance was misplaced. Shopko
    programmed its computer system, PDX Adjudication
    Software System, to systematically exploit the disparity
    between the pharmaceutical prices negotiated by private
    insurers and those negotiated by Medicaid. The PDX system
    (and the apparently identical system, Condor, used by
    Shopko’s subsidiary Pamida) submits claims to a dual-
    eligible’s private insurer first, at the low negotiated rate.
    PDX subsequently but virtually simultaneously adjusts the
    initial price upward to the higher one negotiated by
    Medicaid and bills Medicaid for any unpaid differential, not
    just the co-pay that the dual-eligible owes under his or her
    private insurance contract.
    An example similar to that provided by Thulin during
    oral argument helps illustrate the scheme. Assume for
    instance that a dual-eligible has a prescription for Drug A,
    which has a list price of $50. Her private insurer has an
    agreement with Shopko pursuant to which Shopko has
    agreed to accept $25 as payment in full for Drug A: $20 from
    the private insurer and a $5 co-pay from the dual-eligible.
    Under Medicaid’s less favorable agreement with Shopko,
    Medicaid has agreed to pay $30 for Drug A. The dual-
    eligible submits her prescription to Shopko and pays
    nothing at the point of sale. Shopko fills the prescription and
    then bills the private insurer $25 using PDX. The private
    No. 13-3638                                                  5
    insurer remits payment of $20, the agreed amount of its
    payment less the dual eligible’s unpaid copay. Shopko then
    bills Medicaid, the “payer of last resort,” but not only for the
    $5 that remains unpaid under its contract with the dual-
    eligible’s private insurer. Instead, Shopko bills Medicaid $10,
    the difference between the $20 that the private insurer
    already has paid and the $30 that Medicaid has agreed to
    pay for the drug.
    Thulin alleges that this “internal program of the two
    systems bills more for dual eligible patients than was
    allowed under the assignment of rights and benefits
    provisions of federal law and contract provisions of private
    insurance companies.” That is, Shopko committed fraud by
    billing Medicaid an amount in excess of the co-pay that the
    dual-eligibles owed under their private insurance contracts.
    Shopko compounded this alleged fraud by omitting from its
    invoices to Medicaid the amount of dual-eligibles’ co-pays.
    By omitting this information, Thulin alleges, “Shopko failed
    to report truthfully to Medicaid the nature and extent of [its]
    obligation.”
    Thulin discovered the alleged fraud by observing “that
    there is potential for fraudulent billing involving dual
    eligible patients” and “that the PDX pharmacy system used
    by Shopko does not present the billing and payment amount
    information on the patient bag receipts and it does not make
    it available to the pharmacist or technician processing
    prescriptions.” Thulin nonetheless managed to obtain and
    attach to his complaint 31 printouts from the PDX system
    that allegedly demonstrate the two-pronged fraud. All 31
    exhibits concern transactions performed in Idaho.
    6                                                No. 13-3638
    Yet Thulin filed his suit not in Idaho but in the Western
    District of Wisconsin, and did not bring any claims under
    Idaho law. Instead, he filed one claim under the federal False
    Claims Act (“FCA”), 
    31 U.S.C. § 3729
    , et seq., and eight
    analogous state law claims under the laws of California,
    Illinois, Indiana, Michigan, Minnesota, Montana, Tennessee,
    and Wisconsin. The attorneys general of the affected states
    and the federal government declined to intervene in Thulin’s
    qui tam suit. Thulin then elected to continue the suit on their
    behalf, see 
    31 U.S.C. § 3730
    (c)(3), and Shopko moved to
    dismiss all of his claims.
    The district court granted Shopko’s motion to dismiss
    Thulin’s federal claim with prejudice. The district court first
    concluded that Thulin failed to allege the requisite falsity to
    state a claim under the False Claims Act because neither 42
    U.S.C. § 1396k(a)(1)(A) nor its related regulations were
    applicable to Shopko and Thulin “fail[ed] to explain how the
    assignment law applies to Shopko in the first instance or
    provide any support for his legal claim.”
    The district court also concluded that Thulin’s allegations
    pertaining to the knowledge element of the claim failed to
    meet the requirements of Federal Rule of Civil Procedure 8,
    let alone Rule 9(b). The court concluded that “[t]o the extent
    plaintiff is alleging that Shopko knows that the assignment
    law applies to it as a provider (rather than pleading that it
    knows the prices it negotiates with private health insurers),
    the pleading is not at all clear.” Moreover, “[n]either does
    plaintiff allege facts to support how Shopko knows of such
    an obligation, nor who in the organization has actual
    knowledge.” The district court further faulted Thulin for
    pointing to a Minnesota regulation in his complaint but not
    No. 13-3638                                                  7
    “alleg[ing] any individual transactions in Minnesota as
    required to meet the pleading requirement of Rule 9(b).”
    The district court declined to exercise supplemental
    jurisdiction over Thulin’s state law claims and dismissed
    them without prejudice. Thulin timely appealed.
    II.
    We review de novo the district court’s grant of a motion to
    dismiss. Camasta v. Jos. A. Bank Clothiers, Inc., 
    761 F.3d 732
    ,
    736 (7th Cir. 2014). To survive a motion to dismiss under
    Rule 12(b)(6), a complaint must provide enough factual
    information to “state a claim to relief that is plausible on its
    face” and “raise a right to relief above the speculative level.”
    Bell Atl. Corp. v. Twombly, 
    550 U.S. 544
    , 555, 570, (2007).
    Whether a complaint states a claim upon which relief may be
    granted is depends upon the context of the case and
    “requires the reviewing court to draw on its judicial
    experience and common sense.” Ashcroft v. Iqbal, 
    556 U.S. 662
    , 679, (2009). We accept the complaint’s well-pleaded
    facts as true and construe the allegations in the light most
    favorable to the plaintiff. Camasta, 761 F.3d at 736. However,
    “[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 a footnote midway through his opening brief, Thulin
    requests that we confine our review to the allegations in his
    complaint and ignore the numerous exhibits that Shopko
    attached to its motion to dismiss. This is of course how both
    we and the district court generally analyze motions to
    dismiss. See Fed. R. Civ. P. 12(d). However, in this case, the
    district court considered and relied upon several of the
    8                                                  No. 13-3638
    documents that Shopko attached to its motion, as well as
    extra-pleading documents submitted by Thulin. The district
    court concluded that doing so was appropriate because the
    documents were public records of which it could take
    judicial notice without converting the motion to dismiss into
    one for summary judgment. See Ennenga v. Starns, 
    677 F.3d 766
    , 773-74 (7th Cir. 2012). Thulin does not challenge this
    conclusion, nor does he clarify which, if any, of Shopko’s
    documents improperly were considered on this basis.
    Moreover, he called the issue to our attention only by way of
    a footnote, see Long v. Teachers’ Ret. Sys. of Ill., 
    585 F.3d 344
    ,
    349 (7th Cir. 2009) (“A party may waive an argument by
    disputing a district court’s ruling in a footnote.”), and relies
    upon his own extra-pleading submissions. In light of all
    these circumstances, we cannot (and do not) conclude that
    any procedural error by the district court gave rise to
    anything other than a no-harm, no-foul situation.
    Thulin correctly concedes that he must satisfy the
    heightened pleading standard imposed by Federal Rule of
    Civil Procedure 9(b). See United States ex rel. Gross v. AIDS
    Research Alliance-Chicago, 
    415 F.3d 601
    , 604 (7th Cir. 2005)
    (“The FCA is an anti-fraud statute and claims under it are
    subject to the heightened pleading requirements of Rule
    9(b).”). We need not overly concern ourselves with the
    adequacy of Thulin’s pleading, however, as we agree with
    the district court that his legal theory is not viable no matter
    how detailed his factual allegations.
    Thulin brought his claims under the FCA, a statute that
    permits private citizens, called relators, to prosecute qui tam
    suits “against alleged fraudsters on behalf of the United
    States government.” United States ex rel. Watson v. King-
    No. 13-3638                                                   9
    Vassel, 
    728 F.3d 707
    , 711 (7th Cir. 2013); 
    31 U.S.C. § 3730
    . The
    United States may choose to intervene in these suits. 
    31 U.S.C. § 3730
    (b)(2). If the United States declines, as
    happened in this case, the relator may pursue the case on his
    own (although still technically on behalf of the United
    States). King-Vassel, 728 F.3d at 711; 
    31 U.S.C. § 3730
    (c)(3).
    “Under either option, if the prosecution of the alleged
    fraudster is successful, the relator can receive a substantial
    award for bringing the false claim to light.” King-Vassel, 728
    F.3d at 711; 
    31 U.S.C. § 3730
    (d)(1)-(2).
    The version of the FCA that was in effect at the time of
    Shopko’s alleged conduct imposed civil liability on “any
    person who knowingly presents, or causes to be presented,
    to an officer or employee of the United States Government or
    a member of the Armed Forces of the United States a false or
    fraudulent claim for payment or approval.” 
    31 U.S.C. § 3729
    (a)(1); see United States ex rel. Lusby v. Rolls-Royce Corp.,
    
    570 F.3d 849
    , 855 n.* (7th Cir. 2009). The current version of
    another provision of the FCA – which “applies to cases such
    as this, that were pending on or after June 7, 2008,” United
    States ex rel. Yannacopoulos v. Gen. Dynamics, 
    652 F.3d 818
    , 822
    n.2 (7th Cir. 2011) – also imposes liability upon “any person
    who knowingly makes, uses, or causes to be made or used, a
    false record or statement material to a false or fraudulent
    claim.” 
    31 U.S.C. § 3729
    (a)(1)(B). Thus, “[t]o establish civil
    liability under the False Claims Act, a relator generally must
    prove [at this stage of the case, allege] (1) that the defendant
    made a statement in order to receive money from the
    government; (2) that the statement was false; and (3) that the
    defendant knew the statement was false.” Yannacopoulos,
    
    652 F.3d at 822
    . The penalties imposed upon those who are
    liable under the FCA range from $5,000 to $10,000, “plus 3
    10                                                No. 13-3638
    times the amount of damages which the Government
    sustains.” 
    31 U.S.C. § 3729
    (a)(1)(G); King-Vassel, 728 F.3d at
    711.
    Here, there is no dispute that Thulin adequately pleaded
    the first element by alleging with particularity that Shopko
    submitted claims to the federal government via the Medicaid
    program. King-Vassel, 728 F.3d at 711. The next element is
    that the claims were false. A claim may be false for purposes
    of the FCA if it is made in contravention of a statute,
    regulation, or contract. See United States ex rel. Crews v. NCS
    Healthcare of Ill., Inc., 
    460 F.3d 853
    , 858 (7th Cir. 2006).
    Thulin’s theory of falsity is predicated upon 42 U.S.C. §
    1396k(a)(1)(A), which he refers to as the “Federal
    Assignment Law.” This provision states:
    For the purpose of assisting in the collection of
    medical support payments and other payments
    for medical care owed to recipients of medical
    assistance under the State plan approved under
    this subchapter, a State plan for medical
    assistance shall – provide that, as a condition of
    eligibility for medical assistance under the State
    plan to an individual who has the legal
    capacity to execute an assignment for himself,
    the individual is required – to assign the State
    any rights, of the individual or of any other
    person who is eligible for medical assistance
    under this subchapter and whose behalf the
    individual has the legal authority to execute an
    assignment of such rights, to support (specified
    as support for the purpose of medical care by a
    No. 13-3638                                                 11
    court or administrative order) and to payment
    for medical care from any third party.
    Thulin interprets this provision, along with a similarly
    worded regulation codified at 
    42 C.F.R. § 433.145
    (a), to mean
    that “the government obtains the rights and benefits of the
    private health insurance for these dual-eligible patients,”
    including their right to the lower prescription drug costs that
    their private insurers have negotiated with Shopko. Under
    this view, Medicaid had a right to pay only the lower
    negotiated cost of the drug that Shopko agreed to accept
    from the private insurer, and Shopko violated the “Federal
    Assignment Law” each time it sought payment for any
    amount in excess of the co-pay (which, according to Thulin,
    it also had an obligation to notify Medicaid of).
    Thulin’s strained interpretation has little if any support
    in the plain language of the provision, which by its terms
    applies only to a beneficiary’s right to actually receive
    payments. And Thulin has not pointed to – and we could
    not find – any case law that interprets 42 U.S.C. §
    1396k(a)(1)(A) as he does. Instead, the Supreme Court has
    determined that this “Federal Assignment Law” ensures that
    Medicaid is entitled to reimbursement of its medical
    expenditures if a beneficiary receives a settlement or other
    recovery from third-party tortfeasors. See Wos v. E.M.A. ex
    rel. Johnson, 
    133 S. Ct. 1391
    , 1396 (2013) (“Congress has
    directed States, in administering their Medicaid programs, to
    seek reimbursement for medical expenses incurred on behalf
    of beneficiaries who later recover from third-party
    tortfeasors. States must require beneficiaries ‘to assign the
    State any rights * * * to support (specified as support for the
    purpose of medical care by a court or administrative order)
    12                                                No. 13-3638
    and to payment for medical care from any third party.’” 42
    U.S.C. § 1396k(a)(1)(A)); see also Ark. Dep’t of Health & Human
    Servs. v. Ahlborn, 
    547 U.S. 268
     (2006). Perhaps unsurprisingly,
    appeals courts that have examined the statute have
    interpreted it in the same way. See, e.g., Massachusetts v.
    Sebelius, 
    638 F.3d 24
    , 33 n.11 (1st Cir. 2011) (“Whereas 42
    U.S.C. § 1396a(a)(25)(B) imposes an affirmative obligation on
    state Medicaid agencies to seek reimbursement, 42 U.S.C. §
    1396k(a)(1)(A) confers rights upon state Medicaid agencies
    to pursue certain claims as a subrogee.”). We see no reason
    to adopt Thulin’s novel interpretation, and we cannot
    conclude that the district court erred in also declining to do
    so.
    We further note that the extra-pleading evidence
    submitted by the parties—considered by the district court,
    and briefed and argued here—also suggests that Shopko
    was not obligated to inform Medicaid of dual-eligibles’ co-
    pays and was permitted to bill in the fashion that it did. The
    parties discuss at length the electronic system that
    pharmacies were required to use to submit claims to
    Medicaid agencies during the relevant time period, version
    5.1 of the National Council for Prescription Drug Programs
    (“NCPDP 5.1”). See 42 U.S.C. § 1320d-2(a)(1); 
    45 C.F.R. §§ 162.1102
    (a)(1), 162.1801-162.1802. NCPDP 5.1 and its
    “Implementation Guide” provided standard specifications
    for various data inputs relating to Medicaid claims. As is
    relevant here, the pertinent fields related to co-pays were
    labeled optional; other data fields were labeled mandatory
    or “RW,” which means that they were required under
    certain circumstances. Like the district court, we find this
    compelling evidence that pharmacies like Shopko did not
    have an obligation to submit co-pay information to
    Medicaid. If they did, one would think that such an
    No. 13-3638                                              13
    obligation would have been incorporated into the billing
    protocol that they were legally required to use.
    Thulin’s proffered excerpt from the “Q&A” portion of
    the NCPDP only lends further credence to this conclusion, as
    it demonstrates that providers were “looking for
    clarification” on this important billing issue rather than
    simply concluding that they needed to inform Medicaid of
    dual-eligibles’ co-pays. Additionally, the State Medicaid
    Manual promulgated by the Centers for Medicare &
    Medicaid Services directs state Medicaid agencies to
    withhold payment “[w]henever you are billed for the
    difference between the payment received from the third
    party based on [a preferred provider agreement that it has
    with the pharmacy].” Centers for Medicare & Medicaid
    Services, STATE MEDICAID MANUAL § 3904.7 (1990). Thulin is
    correct that this provision supports his contention that
    Medicaid is only liable to the extent that a dual-eligible’s
    private insurer has not paid, but he overlooks the language
    quoted above, which expressly contemplates that Medicaid
    will get billed for amounts beyond what it technically owes
    and bears responsibility for not paying when that happens.
    Shopko’s alleged actions may “frustrate and derail the ‘cost
    avoidance’ mandate,” and result in additional bureaucratic
    hassle on both Medicaid’s and Shopko’s end, but they are
    not false or fraudulent under the State Medicaid Manual or
    any other regulation or law to which Thulin points.
    Because Thulin’s FCA claim lacks a legal basis as
    pleaded, it is inherently implausible and properly was
    dismissed. For the sake of completeness, we briefly address
    Thulin’s argument concerning the adequacy of his
    allegations that Shopko “knew” it was submitting false
    14                                                No. 13-3638
    claims. To be liable under the FCA, Shopko must have acted
    with “actual knowledge,” or with “deliberate ignorance” or
    “reckless disregard” to the possibility that the claims it
    submitted were false. King-Vassel, 728 F.3d at 712; 
    31 U.S.C. § 3729
    (a)(1)(A), (b). Thulin contends that his complaint
    plausibly suggested that Shopko acted with “reckless
    disregard” as we defined the term in King-Vassel, 728 F.3d at
    712-13, because he alleged that Shopko is a “sophisticated,”
    “multi-regional” business that developed and programmed
    the PDX system and should have been aware of federal
    statutes and regulations governing the submission of claims
    to Medicaid. In reaching a contrary conclusion, Thulin
    contends, the district court must have ignored King-Vassel’s
    explication of “reckless disregard.” We disagree. Thulin’s
    allegations would not be sufficient to satisfy his pleading
    requirement even if Shopko’s billing practices were contrary
    to the “Federal Assignment Law.” Although “[m]alice,
    intent, and other conditions of a person’s mind may be
    alleged generally,” Fed. R. Civ. P. 9(b), vague allegations
    that a corporation acted with reckless disregard—i.e., grossly
    negligently or with reason to know of facts that would lead a
    reasonable person to realize that it was submitting false
    claims, see King-Vassel, 728 F.3d at 713—simply by virtue of
    its size, sophistication, or reach do not clear even this lower
    pleading threshold. Such allegations may suggest a
    possibility that Shopko acted with reckless disregard, but
    they do not “nudg[e]” Thulin’s claims “across the line from
    conceivable to plausible.” Iqbal, 
    556 U.S. at 680
    .
    III.
    For all of the reasons stated above, the judgment of the
    district court is AFFRIMED.