MEMORANDUM AND ORDER ON DEFENDANTS’ MOTION TO DISMISS CORRECTED CONSOLIDATED AMENDED CLASS ACTION COMPLAINT AND SECOND AMENDED CONSOLIDATED COMPLAINT 1
Plaintiffs, who are cancer patients and health care plans, accuse defendants Abbott Laboratories (Abbott), Takeda Chemical Industries, Ltd. (Takeda), and TAP Pharmaceutical Products, Inc. (TAP) of conspiring to artificially inflate the price of the drug Lupron® in violation of the civil provisions of the Racketeer Influenced and Corrupt Organizations Act (RICO), 18 U.S.C. § 1962. 2 The class action plaintiffs consist of a commercial health insurance carrier (Beacon Health Plan), an ERISA plan (Twin Cities Bakery Workers Health and Welfare Fund), and four patients who paid for all or part of a Lupron® injection. The class action cases were consolidated in this court by the Multi-District Litigation Panel (MDLP). A coalition of Blue Cross/ Blue Shield Plans, 3 which filed two Lu-pron®-related non-class action cases in the District of Massachusetts then agreed to coordinate pretrial proceedings with the class action plaintiffs, as did the non-class action plaintiff Cobalt Corporation. The plaintiffs collectively seek to recover from the defendants the alleged overcharges for Lupron® as well as punitive damages. Defendants, challenging the legal sufficiency of the plaintiffs’ claims, move to dismiss the combined actions in their entirety. 4
BACKGROUND
The background is summarized from the court’s decision in
Lupron Marketing and Sales Practices Lit.,
On October 16, 2001, TAP plead guilty to violating the Prescription Drug Marketing Act, 21 U.S.C. §§ 331(t), 333(b). 5 TAP admitted that it had encouraged doctors to falsely bill Medicare for free samples of Lupron® as part of a scheme to induce doctors to prescribe Lupron®. TAP was ordered to pay a criminal fine of $290 million. As part of a civil settlement, TAP agreed to pay $559,483,560 in restitution to the United States for losses incurred by Medicare and $25,516,440 in restitution for losses incurred by state Medicaid programs.
Medicare was created in 1965 by Congress to provide medical insurance to senior citizens (ages 65 and older). See 42 U.S.C. §§ 1395 — 1395ggg. Medicare is overseen by the Secretary of Health and Human Services (HHS) and is administered by the Centers for Medicare and Medicaid Services (formerly the Health Care ‘Financing Administration [HCFA]). Medicare Part B pays for a number of medical services, including the cost of certain prescription drugs. While Medicare Part B does not for the most part pay for self-administered drugs, it does pay providers for up to 80% of the “allowable cost” of physician-injected drugs like Lupron®. The remaining 20% is paid by the Medicare beneficiary as a “co-payment.” 6
“Allowable cost” was defined by HHS regulations until 1998 as the lesser of a drug’s estimated actual acquisition cost or its national average wholesale price (AWP). 42 C.F.R. § 405.517. 7 Medicare administrators historically relied on the AWP in setting the reimbursement rate for Lupron®. The AWP in turn was derived by HHS from the Drug Topics Red Book (Red Book), an industry publication compiling wholesale drug prices. The AWP for Lupron® as it appeared in the Red Book was supplied by TAP. No independent verification of the actual AWP was undertaken by Medicare or by the Red Book itself. The published AWP for Lupron® as reported by TAP ranged from $418.75 in 1992 to $623.79 in 2001. 8
After TAP’s guilty plea, putative class actions were brought in various courts on behalf of co-paying beneficiaries, direct purchasers of Lupron®, and private health care plans who were not part of the civil settlement negotiated by the United States. The actions pending in the federal district court were consolidated by the *160 MDLP in the District of Massachusetts for pretrial proceedings. 9 In addition, two cases filed on behalf of the Blues in the District of Massachusetts were joined as related cases. 10
THE AMENDED COMPLAINT
Plaintiffs’ core allegation is that the AWPs for Lupron® reported by the defendants bore no resemblance to the actual prices charged by TAP to doctors, nor did they bear any relationship to a reasonable interpretation of the terms “average” or “wholesale.” The AWPs rather were deliberately inflated as part of an improper marketing and sales scheme to promote Lupron® at plaintiffs’ expense by funneling hidden profits to doctors. As summarized in the Consolidated Complaint:
[t]he improper marketing and sales practices include[d], inter alia: (a) deliberately and falsely overstating the [AWP] for Lupron®, the rate upon which Medicare and private health insurance reimbursement rates are set, so that Medicare, Medicare beneficiaries and the [health care] Plans paid artificially inflated prices for Lupron®; (b) providing free samples of Lupron® to medical providers and instructing them that they could and should bill Medicare and third-party payers for the free samples with the intent that they do so; (c) providing other unlawful financial inducements and hidden price discounts to medical providers to prescribe Lupron®, causing the Plans to pay the artificially inflated price for Lupron®; and (d) actively concealing and causing others to conceal, information about the true price being charged for Lupron®.
Id. ¶ 4. 11
Central to the factual allegations of the Amended Complaint is TAP’s concession that its sales representatives had distributed some $31 million in “free” Lupron® samples between 1993 and 1999. 12 TAP’s president, Thomas Watkins, admitted
that TAP provided free samples of Lu-pron® to a number of physicians, primarily in the early to mid-1990s, with the knowledge that those physicians would seek and receive reimbursement. The billing for free samples is wrong, and it should never have happened.
Class Action Complaint ¶ 83. Dr. Joel Ol-stein, a urologist in Lewiston, Maine, stated that TAP had presented him with a free sample of Lupron® every time that he *161 started a new patient on the drug. “They wanted me to carefully track how many new patients I started on Lupron® and we kept lists. Anybody in practice knows how to bill for free samples.” Id. at ¶ 95.
Plaintiffs allege that defendants offered other undisclosed financial inducements to doctors to stimulate the sales of Lupron®, including volume discounts, rebates, purported “education” grants, junkets, off-invoice pricing, free goods, credit memos, consulting fees and debt forgiveness. In 1996, the Tufts Health Maintenance Organization decided to switch its prostate cancer patients from Lupron® to a less costly competitor drug, Zoladex®. In response, TAP’s national accounts manager, Janice Swirski, told Tufts that TAP could not make any further reduction in the price charged to Tufts, as that would affect the price TAP charged the federal government for Lupron®. Instead, TAP offered Tufts unrestricted “educational grants” of up to $25,000 per year if Tufts would continue to prescribe Lupron® to patients. Tufts declined TAP’s offer.
TAP also forgave debt as a disguised form of illegal discounting. One urology practice in Boston had $11,000 of prior Lupron® debt cancelled in exchange for switching all of its patients from Zoladex® to Lupron®. In 1995, Kimberlee Chase, a TAP sales representative discharged $ 13,-000 of Lupron® debt owed by a urology practice in Fall River, Massachusetts, when the group (which owed TAP in excess of $70,000) threatened to switch its patients from Lupron® to Zoladex®.
Under the guise of business review meetings, TAP devised a so-called “Return to Practice” program to demonstrate how doctors could profit from the spread between the AWP for Lupron® and the actual price that they would be charged for the drug. In one case, a TAP employee left a spread sheet with a Massachusetts urologist who had switched to the less costly Zoladex® showing an additional profit of $7,000 that the doctor could earn by billing the AWP for Lupron®. On another occasion, TAP executives increased the AWP for Lupron® to counter an announced rise in the AWP for Zoladex®.
TAP sales representatives routinely counseled doctors to conceal from patients, insurance carriers, Medicare, and other doctors, the actual price that they paid for Lupron®. Alan Mackenzie, a senior TAP marketing executive, instructed his sales force to caution doctors “that if [they] disclosed their invoice costs to the Medicare Program, that Program would take steps to reduce the maximum payment allowed for Lupron® and thus reduce [their] profit for Return to Practice.” Class Action Complaint at ¶ 112. He further told his sales people to warn doctors that “by discussing your costs of Lupron® with other physicians, you run the risk of that information getting back to [HHS]. If [HHS] then realizes that AWP is not a true reflection of the price, the AWP could be affected, thus lowering the amounts you may charge.” Id. The only pricing information for Lupron® that TAP publicly disclosed was the inflated AWP.
DISCUSSION
The Standard of Revieto
When reviewing a motion to dismiss, “[w]e must accept the allegations of the complaint as true, and if, under any theory, the allegations are sufficient to state a cause of action in accordance with the law, we must deny the motion to dismiss.”
Vartanian v. Monsanto Company,
Political Question
Defendants argue as a preliminary matter that the Amended Complaint should be dismissed under the political question doctrine for lack of justiciability. As explained by Justice Brennan in
Baker v. Carr,
[pjrominent on the surface of any case held to involve a political question is found (1) a textually demonstrable constitutional commitment of the issue to a coordinate political department; or (2) a lack of judicially discoverable and manageable standards for resolving it; or (3) the impossibility of deciding without an initial policy determination of a kind clearly for nonjudicial discretion; or (4) the impossibility of a court’s undertaking independent resolution without expressing lack of the respect due coordinate branches of government; or (5) an unusual need for unquestioning adherence to a political decision already made; or (6) the potentiality of embarrassment from multifarious pronouncements by various departments on one question.
Id.
at 217,
Defendants argue that the fourth of Justice Brennan’s categories (disrespect for decisions taken by the coordinate branches) is implicated by the Amended Complaint. Defendants maintain that Congress has spent decades wrestling over the cost structure of the Medicare program and, despite being aware of the fact that the AWP for most prescription drugs does not reflect their actual cost, “has repeatedly, consciously, and intentionally left the current system in place, leading to the inescapable conclusion that Congress intends AWP to be higher than the cost charged to providers.” Defendant’s Memorandum, at 31. Defendants accuse plaintiffs of now attempting an “end run around the political system” by trying to accomplish in the courts what they have failed to obtain in the political process. For the court to intervene and “second-guess” the decisions of Congress and the HHS regulators would, in the eyes of defendants, “be inappropriate and inadvisable.” 13 Id. at 32.
While an elegant doctrine, political question considerations have generally led to judicial abstention only in sensitive matters relating to national defense and only then in the rarest of cases. As Professor Tribe notes, the Supreme Court has invoked the political question doctrine only twice since
Baker v. Carr
to hold an issue nonjusticiable.
14
See Gilligan v. Morgan,
Moreover, I do not agree with the premise of defendants’ argument that a judicial resolution of this case would entail any disrespect to the intent of Congress in structuring prescription drug reimbursement rates using the AWP as a benchmark. As defendants portray the Congressional purpose in setting the reimbursement rate at 95% of AWP, Congress meant to turn a blind eye to the inflated AWPs as a means of enticing physicians to treat Medicare patients. In other words, Congress deliberately invited the very fraud of which defendants are accused. As defendants describe it, “a determination that AWP must be set at the actual cost to providers would result in lower Medicare payment levels to physicians, prompting many of those physicians to stop treating Medicare patients because it is not cost-effective for them to do so.” Defendants’ Memorandum, at 32. The suggestion that Congress would deliberately condone a bribery scheme using public funds to enrich drug manufacturers and physicians is, to say the least, unusual. 15 It is far more likely that by setting the Medicare reimbursement rate below the AWP, Congress took a tentative step towards using Medicare’s purchasing power as a means of driving down the cost of prescription drugs to the Medicare program. “Average,” after all, means that in a competitive market, some prices will be higher and some lower than the median. Congress might reasonably have wished to put Medicare on the lower rung of the equation. 16
The RICO Claims
A successful civil RICO action requires proof of four elements: “(1) conduct (2) of an enterprise (3) through a pattern (4) of racketeering activity.”
Sedima, S.P.R.L. v. Imrex Co.,
Plaintiffs’ RICO Theories
Count I, which plaintiffs label the “Tap Enterprise,” alleges that Abbott and Take-da, as “persons” within the meaning of 18 U.S.C. § 1962(c), conducted the affairs of TAP, the “enterprise,” through a pattern of racketeering activity consisting of predicate acts of mail and wire fraud. Under this theory, Abbott and Takeda were the decision-makers who jointly determined *165 the price at which Lupron® would be sold by TAP to medical providers as well as the AWP that determined the ultimate cost of the drug to plaintiffs. Abbott and Takeda are also alleged to have directly controlled the marketing of Lupron® by TAP and to have implemented the scheme to distribute free samples of Lupron®. Count II proposes a variant of Count I in which TAP, Abbott, and Takeda (as “persons”) conducted the same racketeering activity through an association-in-fact (the “enterprise”) consisting of themselves and their agents and employees. Count III expands the association-in-fact to include all of the physicians in the United States who participated in the Lupron® marketing scheme. Finally, Count IV alleges that Abbott, Takeda, and TAP conspired to commit RICO offenses in violation of section 1962(d) of the statute.
Defendants’ joint motion to dismiss maintains that the Amended Complaint fails to plead with sufficient specificity facts establishing the necessary predicate acts, the existence of a viable enterprise, causation, and detrimental reliance. I will discuss each of these arguments in the sequence in which they are raised.
Racketeering Acts
Without viable predicate acts a RICO claim collapses.
Ahmed,
Fraud is a concept which by “universal recognition ... is to be construed very broadly.” 2 Sand Siffert, Loughlin & Reiss,
Modern Federal Jury Instructions
¶ 44.01, at 44-11 (2003) (Sand). The concept is not, however, completely unbounded — since
McNally v. United States,
In some circumstances a failure to disclose material information may constitute fraud.
Putting aside the scienter element in fraud and looking only at behavior, the locus classicus of fraud is a seller’s affirmative false statement or a half truth, *166 i.e., a statement that is literally true but is made misleading by a significant omission. See Emery v. American Gen. Fin., Inc.,71 F.3d 1343 , 1348 (7th Cir.1995) (Posner, C.J.). At common law, fraud doctrine did not impose any broader, general duty to disclose, see Chiarella v. United States,445 U.S. 222 , 228,100 S.Ct. 1108 ,63 L.Ed.2d 348 (1980), but it is settled that the mail and wire fraud statutes go somewhat beyond the common law, see McEvoy Travel Bureau, Inc. v. Heritage Travel, Inc.,904 F.2d 786 , 791 (1st Cir.1990). Thus, a leading commentary on federal jury instructions says that even where there is no falsehood or half truth:
[T]he failure to disclose information may also constitute a fraudulent representation [under the mail and wire fraud statutes] if the defendant was under a legal, professional or contractual duty to make such a disclosure. ...
Bonilla v. Volvo Car Corp.,
Defendants seize on the duty issue arguing that their Lupron® marketing efforts were directed to medical providers and not to the plaintiffs to whom they owed no fiduciary or contractual duty of disclosure. As defendants characterize the pleadings, “[a]t bottom, [plaintiffs’ complaint is that [defendants did not disclose to them the price at which third parties purchased Lu-pron.” Defendants’ Memorandum, at 15. Defendants cite
Bonilla, supra,
as a case squarely on point. Plaintiffs in
Bonilla
brought a RICO complaint objecting to Volvo’s practice of adding accessories and emblems to vehicles after they had been shipped to market and then selling them as upgraded models, and (perhaps more to the point), charging different prices for the same car in different markets. As to the first allegation, the First Circuit concluded that Volvo owed no duty to disclose to customers where the add-on emblems and accessories had been installed. While acknowledging the existence of a “shadowy area ... in which conduct alone, in context, can amount to a misrepresentation,”
Bonilla,
Defendants see a perfect eongruity between their conduct and that of the vindicated Volvo Car Corporation. “Plaintiffs cannot contend that [defendants owed them any professional, fiduciary, contractual, or other legal duty to disclose Lu-pron’s pricing structure.... To the contrary, there is no duty to disclose pricing structures to consumers, and courts have dismissed RICO claims for that very reason.” Defendants’ Memorandum, at 17. As further support, defendants cite
Langford v. Rite Aid of Alabama, Inc.,
A good argument can go wrong when its fundamental premise is flawed. It is true, as defendants contend, that no federal case or statute imposes a duty on a manufacturer to disclose to retail consumers the prices that it charges intermediate suppliers for its products, nor with a possible antitrust exception, is a seller required to charge the same price for a product to every consumer in every market. This is true even where the seller derives a presumed benefit from the consumer’s ignorance of what it actually paid for the products it sells.
See Alves v. Harvard Pilgrim Health Care, Inc.,
204 F.Supp.2d. 198, 212-214 (D.Mass.2002) (Saris, J.),
aff'd,
But this is not a case of nondisclosure. Defendants did not stand mute. As alleged in the Amended Complaint, defendants trumpeted a lie by publishing the inflated AWPs, knowing (and intending) them to be used as instruments of fraud. Whether one views the defendants’ actions as involving the dissemination of information that was wholly false, or false because of an incomplete depiction of the truth, they are actionable under the mail and
*168
wire fraud statutes.
18
Nor does it matter that defendants may not have specifically intended to deprive the plaintiffs of their money. In
United, States v. Christopher,
Turning to whether we should now adopt a convergence theory, we see little reason to do so. Nothing in the mail and wire fraud statutes requires that the party deprived of money or property be the same party who is actually deceived. The phrase “scheme or artifice ... for obtaining money or property by means of false or fraudulent pretenses, representations, or promises,” 18 U.S.C. § 1341, is broad enough to include a wide variety of deceptions intended to deprive another of money or property. McNally itself says nothing about convergence. See United States v. Evans,844 F.2d 36 , 39 (2d Cir.1988). We see no reason to read into the statutes an invariable requirement that the person deceived be the same person deprived of the money or property by the fraud.
Id. at 54.
This is not a case of a retailer failing to disclose the discounted prices that it offered to favored customers (Langford), or a manufacturer the price differentials on its sales of the same product in different markets (Bonilla), or a health plan the discounts it received on prescription drugs (Alves). Rather, this is a case of affirmative misrepresentation. And because the alleged misrepresentations were knowing, deliberate, and made in furtherance of a scheme to defraud, they are sufficient to support the predicate acts of mail and wire fraud. 19
*169 Lack of Particularity
The defendants’ second argument alleges a failure on plaintiffs’ part to plead fraud with particularity. More precisely, defendants complain that the plaintiffs have failed in the Amended Complaint to “set forth the time, place, content or individuals responsible for the supposed mail or wire fraud,” and rely instead on generic assertions that marketing, sales, and other documents were disseminated by mail and wire. Defendant’s Memorandum, at 20.
See Feinstein,
In contrast, the Amended Complaint alleges a course of protracted conduct on the defendants’ part that virtually spanned the ten years from the introduction of Lu- *170 pron® to the American market to TAP’s g-uilty plea in 2001. It is true, as defendants contend, that the Amended Complaint does not identify specific instances of mailings, or the use of facsimile transmissions, or the telephone. 21 But the Amended Complaint is reasonably specific as to the nature of the materials that are alleged to have been distributed in furtherance of the scheme. See, e.g., Consolidated Complaint ¶ 88 (1996 fraudulent marketing materials), ¶ 108 (1995 fraudulent sales directives), ¶ 150 (national marketing and sales plans). More particularly ¶ 151 specifies eight categories of documents that are alleged to have been disseminated by mail or wire in furtherance of the scheme, including: (1) marketing materials promoting the AWP spread; (2) the submissions of the AWP to the Red Book; (3) communications related to the distribution of free samples; (4) inaccurate credit memos and invoices sent to physicians; (5) communications regarding junkets and the TAP into the Future program; (6) communications with government agencies misrepresenting the AWP; (7) similar misleading communications with patients and health insurers; and (8) the receipt of payments for Lupron®.
“Generally, there are three purposes behind Rule 9(b)’s particularity requirement: (1) to place the defendants on notice and enable them to prepare meaningful responses; (2) to preclude the use of a groundless fraud claim as a pretext to discovering a wrong or as a ‘strike suit’; and (3) to safeguard defendants from frivolous charges which might damage their reputations.”
New England Data Services, Inc. v. Becher,
[I]n a RICO mail and wire fraud case, in regards to the details of just when and where the mail or wires were used, we hold that dismissal should not be automatic once the lower court determines *171 that Rule 9(b) was not satisfied. In an appropriate case, where, for example the specific allegations of the plaintiff make it likely that the defendant used interstate mail or telecommunications facilities, and the specific information as to use is likely in the exclusive control of the defendant, the court should make a second determination as to whether the claim as presented warrants the allowance of discovery and if so, thereafter provide an opportunity to amend the defective complaint. We advocate this procedure because of the apparent difficulties in specifically pleading mail and wire fraud as predicate acts. In the instant case, it is seemingly impossible for the plaintiff to have known exactly when the various defendants phoned or wrote to each other or exactly what was said. The plaintiff clearly set out á general scheme, which very plausibly was meant to defraud the plaintiff, and also probably involved interstate commerce. Assuming the facts as stated in plaintiffs complaint, defendant Monarch Investments is incorporated in a different state than that resided in by the other defendants. In this day and age, it is difficult to perceive how the defendants would have communicated without the use of the mail or interstate wires. See Federal Deposit Insurance Corp. v. Kerr,637 F.Supp. at 835 (“... it is hard to imagine how such a transaction could be carried out without the use of such interstate devices.”).
Becher,
The Enterprise
As previously stated, plaintiffs posit three theories: (1) TAP as the enterprise, with Takeda and Abbott as the RICO persons; (2) TAP, Abbott, and Takeda as an associational enterprise in fact, with each of the constituent companies acting as a RICO person; and (3) TAP, Abbott, and Takeda as RICO persons, with the doctors who participated in reaping the rewards of the Lupron® marketing scheme serving as an associational enterprise. 24
As to the TAP enterprise, I do not understand defendants to object to the underlying legal theory, but rather to plaintiffs’ alleged failure to plead facts showing how Abbott and Takeda participated in the conduct of the affairs of TAP. The argument merits only one sentence in defendants’ opening brief, and is somewhat difficult to parse, but it appears to simply restate the argument that the alleged acts of mail and wire fraud are plead with insufficient particularity. As I have already rejected that argument, there is nothing left to be said. If defendants are suggesting that plaintiffs have failed to allege facts sufficient to meet the
Reves
standard (that a RICO defendant be shown to have taken “some part in directing the enterprise’s affairs,”
id.,
507 U.S.
*172
at 179,
With respect to the second theory, defendants begin with the accurate observation that a single entity cannot be both a RICO “enterprise” and a RICO “person.”
Hasbro,
Under 1962(c), the enterprise and the “person” who violates the statute must be distinct from each other, the former being exempt from liability, the latter being the targeted defendant. Schofield v. First Commodity Corp. of Boston,793 F.2d 28 (1st Cir.1986). The distinction requirement is not satisfied by merely naming a corporation and its employees, affiliates, and agents as an association-in-fact, since a corporation acts through its employees, subsidiaries and agents, and would thereby be merely associating with itself. Odishelidze v. Aetna Life & Casualty Co.,853 F.2d 21 (1st Cir.1988); Roeder v. Alpha Industries, Inc.,814 F.2d 22 (1st Cir.1987). Where the plaintiffs have suffered harm at the hands of an enterprise that consists only of a *173 single corporation and its employees, subsidiaries or agents, the plaintiffs “must choose between the corporation and its constituents as persons liable.” If the plaintiff chooses to identify the corporation as the enterprise through which its employees, as persons, conducted the RICO activity, the corporation is insulated from liability. It is for this reason that plaintiffs often try to prove the more intricate association-in-fact, in order to save as defendants all the corporate entities in the scheme, often the deep pockets.
Id., 777
F.Supp. at 1054 (some internal citations omitted). It is the latter route indicated by Judge Fuste that plaintiffs have chosen to travel by defining the enterprise as a combination of the three separate companies in an informal association-in-fact, while at the same time defining each defendant in a separate capacity as a RICO person. As a pleading theory, the idea that a defendant may be -both a person and a member of a collective RICO enterprise has substantial support in the reported cases.
See, e.g., United States v. Goldin Indus., Inc.,
Plaintiffs’ third theory is more problematic. Plaintiffs allege a “Physicians Enterprise,” an association-in-fact consisting of TAP and all doctors (and other providers of medical services) who dispensed Lupron® to patients (with the three corporate defendants as the RICO persons).
27
Ah association-in-fact is defined not by a formal legal structure or similar attributes, but by the association of its members “for a common purpose of engaging in a course of conduct.”
Turkette,
Causation
RICO requires “some direct relation between the injury asserted and
*175
the injurious conduct alleged.”
Holmes,
Detrimental Reliance
The essence of defendants’ argument on this element is the absence of any evidence (or substantive allegation) that plaintiffs relied on misrepresentations by the defendants (in the sense that there is no assertion that any plaintiff consulted the published AWP for Lupron® in deciding on a course of treatment or that the benefit plans were unaware that the Lu-pron® AWP as published was pegged higher than its actual cost). While the argument that the common-law requirement of detrimental (justifiable) reliance is an element of a civil RICO case premised on fraud had found significant support in a number of courts at the time defendants’ briefs were filed, it was rejected by the First Circuit in Loiselle.
Perhaps there is some surface incongruity in allowing a civil RICO plaintiff to recover for fraudulent acts even though the same plaintiff could not (for lack of reliance) recover for fraud at common law. But Congress structured its civil remedy to allow recovery for harm caused by defined criminal acts, including violation of section 1341; and, as noted, the federal mail fraud statute does not require reliance. Thus, under a literal reading of RICO — the presumptive, choice in interpretation — nothing more than the criminal violation and resulting harm is required.
Id.,
Conspiracy
To establish a RICO conspiracy under section 1962(d), plaintiffs must show: “(1) the existence of enterprise affecting interstate commerce, (2) that the defendant knowingly joined the conspiracy to participate in the conduct of the affairs of the enterprise, (3) that the defendant participated in the conduct of the affairs of the enterprise, and (4) that the defendant did so through a pattern of racketeering activity by agreeing to commit, or in fact committing, two or more predicate offenses.”
Aetna Casualty,
State Consumer Protection Act Claims
Preemption
Defendants’ principal challenge to plaintiffs’ consumer protection act claims is predicated on the argument that they are preempted by the Medicare Act, and in the case of plaintiff Twin Cities, by the federal Employee Retirement Security Act (ERISA), 29 U.S.C. § 1144(a). Defendants’ preemption argument has two facets, both based on the doctrine of implied preemption.
30
Defendants first argue field preemption. “Congress’s intent to occupy a given field can be inferred from the pervasiveness of federal regulation and/or the dominance of the federal interest in a particular area of legislative activity.”
Massachusetts Assoc. of Health Maint. Org. v. Ruthardt,
“Congress’s intent is the touchstone of preemption analysis.... State common law claims may be preempted along with state statutes and regulations, if Congress so intended.”
Mendes v. Medtronic, Inc.,
Here, the fact that Congress has failed to disturb the widespread practice on the part of pharmaceutical companies of grossly overstating their AWPs cannot be read as a clear and manifest intention to grant immunity from state regulation of such fraudulent practices. Because there is no evidence of a clear and manifest intent to preempt the entire field of state regulation of fraudulent medical billing practices, claims based on state consumer protection statutes that allege such practices are not preempted. Cf. Hofler v. Aetna U.S. Healthcare of California, Inc.,296 F.3d 764 , 768 (9th Cir.2002) (“Because Congress did not clearly manifest any intention to convert all state tort claims arising from the administration of Medicare benefits into federal questions, we hold that the Medicare program does not completely preempt state tort law claims.”).
Defendants’ conflict preemption argument fares no better. Defendants essentially misstate the issue. Plaintiffs are not seeking, as defendants claim, a judicial declaration invalidating the use of the Lu-pron® and other AWPs by Medicare regulators as a benchmark for setting reimbursement rates for prescription drugs. What plaintiffs are instead seeking is to punish defendants for fraudulently manipulating the spread between the AWP and the actual cost of the drug and for encouraging doctors to falsely bill for free samples as part of a scheme to promote brand loyalty, ultimately at plaintiffs’ expense. While it is true that a state court will be called upon to draw a line between a reasonable profit and fraudulent conduct in assessing plaintiffs’ damages, this line-drawing exercise has nothing to do with the wisdom of the system Congress has put in place to govern Medicare reimbursements, nor should it. Nor is the exercise itself an exotic adventure. It is the stuff of what courts (and juries) do every day by the very nature of their function. Defendants’ concern that “[i]f [plaintiffs’ state law claims are permitted to go forward, Medicare providers would be forced to contend with the 50 states’ varying laws, as well as Medicare rules, whenever they interact with the federal government regarding the Medicare program,” is a valid one. Defendants’ Memorandum, at 36. However, a degree of unevenness in result is a familiar aspect of a federal constitutional system that respects the sovereign decision-making of its constituent parts. But one would think that a drug company interacting honestly with the federal Medicare regime would have little to fear from the states, whose interest in a sound Medicare program is presumably no less fervent than is that of the federal government, or if abuse did result, that the Supreme Court would hesitate to invoke its constitutional power “to review a state court’s decision of a federal issue in a state cause of action.”
Merrell Dow Pharmaceuticals Inc. v. Thompson,
478 U.S.
*179
804, 816,
Section 514(a) of ERISA, 29 U.S.C. § 1144(a), preempts any and all state claims “related to” an employee benefit plan (except state laws that “regulate insurance.” 29 U.S.C. § 1144(b)(2)(A)). A law “relates to” an ERISA-covered plan if it has a connection with or makes reference to such a plan.
Cal. Div. of Labor Standards Enforcement v. Dillingham Constr., N.A., Inc.,
Defendants argue that because the claims of ERISA plaintiff Twin Cities concern the payment of benefits, a “core ERISA concern” is implicated. “The [c]ourt would necessarily be required to consult the terms of Twin Cities’ plan to determine whether and to what extent it allegedly overpaid for Lupron.” Defendants’ Memorandum, at 37.
34
Case law, however, uniformly holds that ERISA pre
*180
emption does not bar a plan from bringing a suit against a third party to protect the assets of the plan or the interests of its beneficiaries.
See, e.g., LeBlanc v. Cahill,
As plaintiffs point out, “[hjere, neither the plan administrator, fiduciary, or beneficiary of the plan, nor the employer, is disputing the terms of the benefit plan or the scope of its benefits.” Plaintiffs’ Memorandum, at 50. Nor are defendants “principal players in the ERISA scenario.”
Carpenters Local,
Pleading Sufficiency
Counts V through XV and Counts XVIII and XIX of the Consolidated Complaint assert consumer protection act claims under the law of each of the Blues plaintiffs’ state of incorporation. 35 The statutes are essentially similar in that they authorize a *181 cause of action against a- commercial defendant who is accused of deceptive acts or fraudulent practices. Florida’s Deceptive and Unfair Trade Practices Act, Fla; Stat. Ann. § 501.204, for example, states that “[u]nfair methods of competition, unconscionable acts or practices, and unfair or deceptive acts or practices or practices in the conduct of any trade or commerce are hereby declared unlawful,” while Missouri’s Merchandising Practices Act, Mo. Ann. Stat. § 407.020, prohibits “deception, fraud, false pretense, false promise, misrepresentation, unfair practice or the concealment, suppression, of omission of any material fact in connection with the sale or advertisement of any merchandise.” Mail and wire fraud, the predicate acts underlying plaintiffs’ RICO claims, are by definition unfair and deceptive acts. If plaintiffs are able to prove any one or more of their RICO claims, their ability to satisfy the elements of a consumer protection act claim under any of the referenced statutes will follow almost as a matter of course. 36 Consequently, the motion to dismiss these counts will be denied. 37
Common-Law Fraud
Defendants argue that plaintiffs’ common-law fraud claim, which is based on local law in the state in which each plaintiff resides, is insufficiently plead. Relying on the parties’ briefs, I will assume that there is a commonality among these states in defining the elements of a common-law misrepresentation claim and that Massachusetts would serve as an exemplar in requiring a showing of: (1) the making of a false statement of fact; (2) known by the defendant to be false when made (or believed by the defendant to be so); (3) with the intent that the victim rely on its truth; and (4) upon which the victim did rely in parting with his property.
Commonwealth v. Leonard,
Unjust Enrichment
Unjust enrichment is regarded by most (but not all) states as an equitable claim. Under the doctrine of unjust enrichment a plaintiff seeks restitution of a benefit conferred on another whose retention of the benefit at plaintiffs expense would be unconscionable.
38
To satisfy the five elements of unjust enrichment, a plaintiff must show: “(1) an enrichment, (2) an impoverishment, (3) a relation between the enrichment and the impoverishment, (4) the absence of justification and (5) the absence of a remedy provided by law.”
LaSalle Nat’l Bank v. Perelman,
*183 Statute of Limitations
Defendants finally argue that all untimely claims must be dismissed on statute of limitations grounds because of plaintiffs’ lack of diligence in discovering the facts underlying the Amended Complaint. The statute of limitations for a civil RICO action is four years.
40
Agency Holding Corp. v. Malley-Duff &
Assocs.,
Inc.,
As defendants frame the issue, because the difference between the published AWP and the actual prices charged for Lupron® was a matter susceptible to discovery through reasonable investigation, plaintiffs are unable to invoke the fraudulent concealment rule. The defendants’ best argument in this regard is the fact that within industry and government circles there was a generalized awareness that the AWP exceeded the actual acquisition cost for Lupron®. Plaintiffs maintain that they became aware of the injury only in 2000 when the federal government began disclosing the results of its investigation of the Lupron® marketing scheme. They might also have noted that it was only after prolonged digging with the coercive assistance of a federal grand jury that the government came to the conclusion that the price differential between the AWP and the actual cost of Lupron® to providers was of fraudulent proportions and that the doctors who had benefitted from the false billings for free samples of Lupron® would have been unlikely volunteers in any effort by plaintiffs to unearth the scheme on their own.
Whether a plaintiff knew or should have known of an injury so as to trigger the running of a statute of limitations is, with rare exception, a jury issue.
See Santiago Hodge v. Parke Davis & Co.,
ORDER
For the foregoing reasons, the motion to dismiss is DENIED as to Counts I, II, and IV of the Blues’ Consolidated Complaint and ALLOWED as to Counts III, XVI, and XVII. The motion to dismiss Counts V through XV and Counts XVIII and XIX of the Consolidated Complaint is DENIED. The motion to dismiss Counts I, II, V, and VI of the Class Action Complaint is DENIED. The motion to dismiss to Counts III, IV, VII, and VIII of the Class Action Complaint is ALLOWED.
SO ORDERED.
Notes
. The court previously rejected Takeda's motion to dismiss for want of personal jurisdiction. While the court agreed with Takeda that plaintiffs had failed to establish specific jurisdiction, it held that Takeda was subject to general jurisdiction under the "doing business” test of the Illinois Long-Arm Statute, 735 Ill. Comp. Stat. § 5/2-209(b)(4).
See In re Lupron Marketing and Sales Practices Lit.,
. Plaintiffs also assert claims under various state consumer protection statutes as well as claims of common-law fraud and unjust enrichment.
. The Blue Cross/Blue Shield plaintiffs will be referred to familiarly as the "Blues plaintiffs” in this opinion.
.The Blues’ Second Amended Consolidated Complaint (Consolidated Complaint) largely tracks the class action plaintiffs' Corrected Consolidated Amended Class Action Complaint (Class Action Complaint). Factual allegations have been drawn from both the Consolidated Complaint and the Class Action Complaint. I have used the term "Amended Complaint” to refer collectively to the identical legal theories contained in both Complaints. Counts are discussed using the structure and numbering of the Consolidated Complaint. The term plaintiff includes the class action plaintiffs and the Blues plaintiffs unless otherwise indicated.
. Following TAP's plea, an indictment was unsealed against six present and former TAP employees and a Massachusetts urologist, alleging a criminal conspiracy to defraud the federal Medicare program. Several other urologists were charged in criminal informa-tions.
. Beneficiaries are required to pay an annual deductible before Part B benefits become available. Some Part B participants purchase "Medigap” insurance from the Blues plaintiffs to cover all or part of the co-payment.
. On January 1, 1998, in response to a directive in the Balanced Budget Act of 1997, HCFA amended 42 C.F.R. § 405.517 to redefine the allowable cost as the lower of the actual Medicare billing or 95% of the AWP.
. Despite the published AWPs, the Amended Complaint alleges that the actual cost of Lu-pron® to doctors declined from $340 in 1993 to $207 in 1999. Consolidated Complaint at ¶ 8.
. The lead plaintiffs in six of these cases are named as plaintiffs in the Class Action Complaint. The six cases are: Russano v. TAP Pharmaceutical Products, Inc. (N.D.Ill.C.A. No. 01-6982); Goetting v. TAP Pharmaceutical Products, Inc. (S.D.Ill.C.A. No. 01-703); Porter v. TAP Pharmaceutical Products, Inc. (D.Mass.C.A. No. 01-10861); Beacon Health Plans, Inc. v. TAP Pharmaceutical Products, Inc. (D.Mass.C.A. No. 01-10897); Brickey v. TAP Pharmaceutical Products, Inc. (N.D.Ala.C.A.No.01-2770); and Twin Cities Bakery Workers Health and Welfare Fund v. TAP Pharmaceutical Products, Inc. (D.Minn.C.A. No. 01-2023).
. The Blues cases are Empire Healthchoice, Inc., d/b/a/ Empire Blue Cross and Blue Shield v. TAP Pharmaceutical Products, Inc. (D.Mass. C.A.02-10015) and Blue Cross and Blue Shield of Florida, Inc. v. TAP Pharmaceutical Products, Inc. (D.Mass.C.A.02-10139). On January 14, 2003, the court approved a stipulation adding Oxford Health Plans, Inc., and Horizon Healthcare Services, Inc., as parties to the Consolidated Complaint.
. The class action plaintiffs limn the same elements of the scheme, emphasizing the injury to the members of. the proposed class, including private purchasers of Lupron® and co-paying Medicare beneficiaries.
. The Massachusetts U.S. Attorney estimated that the AWP billings to Medicare for these free samples ranged between $31 million and $61 million. Government's TAP Sentencing Memorandum, at 20-22.
. Defendants also argue that the second of the categories (lack of manageable standards) is also at play as the court without direction from Congress "would have to step into the political arena and malee policy decisions about the Medicare payment level for covered pharmaceuticals.” Id. at 32. This argument seems somewhat overblown. As I understand the Amended Complaint, plaintiffs are not asking the court to determine the appropriate AWP for Lupron®. Rather, they are seeking to recoup the difference between what they paid for Lupron® as a result of the listed AWP and the actual price paid by doctors for the drug, a figure reasonably ascertainable by the plaintiffs without the help of the court.
. 1 L.H. Tribe, American Constitutional Law 376 (3d ed.2000).
. If this were Congress's purpose, one would think it would have been more effective to simply bribe doctors directly without offering drug companies a cut. On the larger issue, I do not understand why a doctor, who is being paid to administer a drug to a patient, is entitled to earn a profit on the drug he injects. A doctor does not earn a commission (or so one hopes) on a drug that he prescribes.
. Defendants also assert that plaintiffs' claims are barred by the filed rate doctrine. The doctrine has several permutations but is usually held to prohibit a regulated entity from charging rates for its services "other than those properly filed with the appropriate regulatory authority.”
See Sithe New England Holdings, LLC v. Federal Energy Regulatory Commission,
. The Langford Court, however, was careful to note that it could “envision many situations in which a failure to disclose information could constitute fraud pursuant to [the mail and wire fraud statutes], even where no duty to disclose exists independently.” Id. at 1313.
. In response to defendants’ no duty to disclose argument, plaintiffs cite numerous cases holding corporations to a duty of full disclosure.
See, e.g., Roeder,
. Defendants repeatedly assert that they had no duty to disclose what was publicly known to everyone, that is, that the Lupron® AWP was a "sticker price” and never intended to reflect the drug’s true average wholesale price. In support of this argument, defendants cite a number of government reports acknowledging that the published AWPs for prescription drugs often exceed their acquisition cost. The argument is ultimately unpersuasive. There is a difference between a sticker price and a sucker price. If one were confronting a modest markup of the actual AWP for Lupron® (which 300% is not), intended to make sales of the drug for the treatment of Medicare patients commercially viable (given the 95% of AWP reimbursement rate), it is unlikely that there would have been a government investigation of TAP's marketing practices. Similarly, if the same inflated *169 AWP had not been used to set reimbursement rates for private purchasers and insurers, the Amended Complaint would not have been filed. The Blues, in their response to defendants' argument, have it exactly right: "[I]f everything [about Lupron®] was known to everybody, why did [d]efendants emphasize secrecy?” Blues Memorandum, at 7. Finally, the recognition on the part of government regulators of inefficiencies in the administration of Medicare does not, as defendants contend, amount to condonation of fraudulent conduct.
. Defendants also cite
DeMauro v. DeMauro,
. This is not always the case. See, e.g., ¶ ¶ 89-90 of the Consolidated Complaint which reference a 1995 interstate conference call in which TAP executives are said to have agreed to increase the spread between Lu-pron®’s AWP and its actual price to maintain a competitive advantage with doctors over a rival drug, Zoladex®.
. Defendants' claim to have learned nothing from the criminal indictments and informa-tions involving Lupron®. The suggestion that they were on notice as a result, according to defendants, "is based on a blatant mischarac-terization of TAP’s plea to a violation of the [Prescription Drug Marketing Act] which had nothing to do with Lupron’s AWP, the primary focus of [pllaintiffs’ claims in this action.” Defendants’ Reply, at 8. This assertion is belied by any fairminded reading of the relevant documents, including the government’s sentencing memorandum. These are replete with references to the manipulation of the Lupron® AWP and the other fraudulent acts that underlie the allegations of the Amended Complaint. I also note the representation by TAP’s counsel at the sentencing hearing that the Chief Executive Officer of TAP (who was present in the courtroom) would communicate to his board the concerns expressed by the sentencing judge regarding the magnitude of the fraud, a board "which is in fact made up of individuals from both Abbott and Takeda.” Dec. 6, 2001 Sentencing Tr., at 33.
. Unlike the case in
North Bridge,
where
Becher
was held not to apply, plaintiffs here (as in
Becher)
have assiduously pursued discovery.
See Feinstein,
. Plaintiffs also allege a section 1962(d) RICO conspiracy involving TAP, Takeda, and Abbott.
. Abbott's Brief, at 9, would elevate the
Reves’
participation test to one of "control” of the enterprise, a significantly higher standard than
Reves
contemplates. "Of course, the word ‘participate’ makes clear that RICO liability is not limited to those with primary responsibility for the enterprise’s affairs, just as the phrase 'directly or indirectly’ makes clear that RICO liability is not limited to those with a formal position in the enterprise, but
some
part in directing the enterprise's affairs is required.”
Id.,
. The Blues plaintiffs, relying on
United States v. Oreto,
. The Class Action Complaint sets out (in Count IV) an “Individual Physician Enterprise” theory. Under this theory, TAP and every individual physician or practice group who participated in the Lupron® marketing scheme would constitute a separate association-in-fact enterprise. Plaintiffs admit that they have no idea of how many, separate actions this theory would entail, but admit that it could be as many as 15,000. Class Action Complaint ¶ 201. Perhaps in response to the court’s criticism of this theory as "totally unmanageable,” the Blues' plaintiffs have omitted this theory from the Consolidated Complaint.
. I do not find the cases which plaintiffs cite in support of the theory to be helpful to their cause. The court in
In re Managed Care Lit.,
. The Amended Complaint is not improved by the borrowing of the concept of conspiracy from a criminal information filed against one urologist who plead guilty to conspiring with TAP. Consolidated Complaint, ¶ 110. While a conspiracy in appropriate circumstances can constitute an association-in-fact,
but see Bachman v. Bear Stearns & Co., Inc.,
Most courts have found that complaints alleging hub-and-spoke enterprises fail to satisfy the RICO enterprise requirement.
See VanDenBroeck v. CommonPoint Mortg. Co.,
. Defendants concede that no Medicare statute or regulation expressly preempts plaintiffs’ state law causes of action.
. Preemption law cautions against a finding that a Congressional act preempts a state law through silence.
Maryland v. Louisiana,
The negative presumption is even stronger when the state law at issue creates a remedy unavailable under federal law. Silkwood v. Kerr-McGee Corp.,464 U.S. 238 , 251,104 S.Ct. 615 ,78 L.Ed.2d 443 (1984); United Construction Workers v. Laburnum Construction Corp.,347 U.S. 656 , 663-64,74 S.Ct. 833 ,98 L.Ed. 1025 (1954); Rice v. Santa Fe Elevator Corp.,331 U.S. at 230 ,67 S.Ct. 1146 . And, it is virtually conclusive when Congress, in the very statute at issue, explicitly pre-empts other stale law remedies but not the remedy at issue. See Cipollone v. Liggett Group, Inc.,505 U.S. 504 , [517-18],112 S.Ct. 2608 ,120 L.Ed.2d 407 (1992).
Schafer v. American Cyanamid Co.,
. Defendants’ reliance on the Congressional mandate imposed by the Medicare, Medicaid, and SCHIP Benefits Improvement Protection Act of 2000 (BIPA), Pub.L. No. 106-554, *178 § 429(a), 114 Stat. 2763 (2000), temporarily forbidding HHS from directly or indirectly decreasing the AWP reimbursement rate as indicating Congress's satisfaction with the present system is somewhat puzzling. BIPA froze the reimbursement rate at 95% of AWP. It did not freeze the published AWPs. Thus, it is not true, as defendants claim, that to conclude "that [defendants overstated or manipulated the AWP for Lupron ..., this [c]ourt would have to rule that state law somehow trumps the [BIPA] directing that no changes be made to Medicare’s reimbursement system.” Defendants’ Reply, at 27. The court would only have to conclude that defendants deliberately misstated the AWP and caused plaintiffs injury as a result. That conclusion implies no conflict whatsoever with the structure of the Medicare reimbursement system.
. I agree with plaintiffs that the preemption concerns reflected in
Buckman Co. v. Plaintiffs’ Legal Committee,
. Defendants also argue that a variance in the method of calculating benefits from state to state would undermine the ERISA objective of establishing nationally uniform plan *180 administration. Id. I frankly do not follow the argument. Benefits already vary from plan to plan and ERISA does not require otherwise.
. The Blues plaintiffs and statutes by Count in the Consolidated Complaint are: (Count V) Empire Blue Cross and Blue Shield — New York Gen. Bus. Law, § 349 ("[djeceptive act or practices in the conduct of any business”); (Count VI) Blue Cross and Blue Shield of Florida — Fla. Stat. Ann. § 501.204 ("[ujnfair methods of competition, unconscionable acts or practices, and unfair or deceptive acts or practices or practices in the conduct of any trade or commerce are hereby declared unlawful”); (Count VII) Trigon — Va.Code Ann. § 59.1-200 ("fraudulent acts or practices committed by a supplier in connection with a consumer transaction”); (Count VIII) Blue Cross and Blue Shield of Kansas City — Mo. Ann. Stat. § 407.020 ("deception, fraud, false pretense, false promise, misrepresentation, unfair practice or the concealment, suppression, or omission of any material fact in connection with the sale or advertisement of any merchandise”); (Count IX) Wellmark — S.D. Codified Laws § 37-24-6 ("deceptive act or practice, fraud, false pretense, false promise, or misrepresentation or to conceal, suppress, or omit any material fact in connection with the sale or advertisement or any merchandise, regardless of whether any person has been mislead"); (Count X) Blue Cross and Blue Shield of Montana — Mont. Code Ann. § 30-14-103 ("unfair or deceptive acts or practices in the conduct of any trade or commerce are unlawful.”); (Count XI) Blue Shield of Cali *181 fornia — -Cal. Bus. & Prof.Code §§ 17203 and 17200 ("any unlawful, unfair or fraudulent business act or practice and unfair, deceptive, untrue or misleading advertising"); (Count XII) Highmark — 73 Pa. Cons.Stat. §§ 201-3, 201-2(4)(xxi) ("[ujnfair methods of competition and unfair or deceptive acts or practices in the conduct of trade or commerce”); (Count XIII) Blue Cross and Blue Shield of Nebraska — Neb. ’ Rev. Stat. § 59-1602 ("[u]n-fair methods of competition and unfair or deceptive acts or practices”); (Count XIV) Blue Cross and Blue Shield of Louisiana — La. Rev. Stat. Ann. § 51:1405 ("[u]nfair methods of competition and unfair or deceptive acts or practices”); (Count XV) Blue Cross and Blue Shield of Tennessee — Tenn. Code Ann. § 47-18-104 ("[u]nfair or deceptive acts or practices affecting the conduct of any trade or commerce”); (Count XVIII) Oxford — Conn. Gen.Stat. Ann. § 42-110b(a) ("unfair methods of competition and unfair or deceptive acts or practices”); and (Count XIX) Horizon — N.J. Stat. Ann. § 56:8-2 ("any unconscionable commercial practice, deception, fraud, false pretense, false promise, misrepresentation, or the knowing concealment, suppression or omission, in connection with the sale or advertisement of any merchandise”). The Class Action Complaint asserts claims under the consumer protection laws of all fifty states and the District of Columbia.
. Defendants make the same argument with respect to these claims as they do with respect to the RICO claims, that they are plead with insufficient particularity to satisfy Rule 9(b). As each claim incorporates the RICO mail and wire fraud allegations of the Amended Complaint, and as I have found those allegations sufficiently plead to satisfy Rule 9(b) insofar as RICO is concerned, it follows that I find that the consumer protection act claims satisfy Rule 9(b) as well.
. In contrast to plaintiffs' common-law fraud claims, none of the specified state consumer protection acts (as best I can determine) requires proof of actual reliance on the deceptive act. They require proof only of a causal connection between the deceptive act and a plaintiff’s loss.
See, e.g., International Fidelity Ins. Co. v. Wilson,
. Where as here what is being claimed is a right to restitution arising from tortious conduct, the more precise term is wrongful enrichment. "Liability in unjust enrichment has in principle nothing to do with fault. It has to do with wealth being in one person’s hands when it should be in another person’s.”
Guyana Tel. & Tel. Co. v. Melbourne Intern.,
. It is, of course, open to plaintiffs to elect the option of proceeding under a theory of unjust enrichment rather than under RICO, but that is a route that I would expect plaintiffs to forego. Even if plaintiffs, under the laws of some states, are permitted to demand both restitution and damages at law, they
*183
would not be allowed to recover cumulative or duplicative damages.
See Guyana Tel. & Tel.,
. The parties agree that the Massachusetts four-year limitations period for consumer protection act claims applies to all of the related state law claims. See M.G.L. c. 260, § 5A.
