Filed: Oct. 12, 2004
Latest Update: Mar. 02, 2020
Summary: Opinions of the United 2004 Decisions States Court of Appeals for the Third Circuit 10-12-2004 In Re: Genesis Precedential or Non-Precedential: Non-Precedential Docket No. 03-2313 Follow this and additional works at: http://digitalcommons.law.villanova.edu/thirdcircuit_2004 Recommended Citation "In Re: Genesis " (2004). 2004 Decisions. Paper 241. http://digitalcommons.law.villanova.edu/thirdcircuit_2004/241 This decision is brought to you for free and open access by the Opinions of the United St
Summary: Opinions of the United 2004 Decisions States Court of Appeals for the Third Circuit 10-12-2004 In Re: Genesis Precedential or Non-Precedential: Non-Precedential Docket No. 03-2313 Follow this and additional works at: http://digitalcommons.law.villanova.edu/thirdcircuit_2004 Recommended Citation "In Re: Genesis " (2004). 2004 Decisions. Paper 241. http://digitalcommons.law.villanova.edu/thirdcircuit_2004/241 This decision is brought to you for free and open access by the Opinions of the United Sta..
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Opinions of the United
2004 Decisions States Court of Appeals
for the Third Circuit
10-12-2004
In Re: Genesis
Precedential or Non-Precedential: Non-Precedential
Docket No. 03-2313
Follow this and additional works at: http://digitalcommons.law.villanova.edu/thirdcircuit_2004
Recommended Citation
"In Re: Genesis " (2004). 2004 Decisions. Paper 241.
http://digitalcommons.law.villanova.edu/thirdcircuit_2004/241
This decision is brought to you for free and open access by the Opinions of the United States Court of Appeals for the Third Circuit at Villanova
University School of Law Digital Repository. It has been accepted for inclusion in 2004 Decisions by an authorized administrator of Villanova
University School of Law Digital Repository. For more information, please contact Benjamin.Carlson@law.villanova.edu.
NOT PRECEDENTIAL
UNITED STATES COURT OF APPEALS
FOR THE THIRD CIRCUIT
No. 03-2313
IN RE:
GENESIS HEALTH VENTURES, INC.,
Debtor
R. STEVEN SCHERFEL
v.
GENESIS HEALTH VENTURES, INC.
JOSEPH MCMAHON,
Trustee
R. Steven Scherfel,
Appellant
Appeal from the United States District Court
for the District of Delaware
(D.C. Civil No. 02-cv-00170)
District Judge: Honorable Joseph J. Farnan, Jr.
Argued April 13, 2004
Before: RENDELL, COWEN and LAY*, Circuit Judges.
(Filed: October 12, 2004)
* Honorable Donald P. Lay, Senior Judge of the United States Court of Appeals for the
Eighth Circuit, sitting by designation.
Philip R. Michael [ARGUED]
Goodkind, Labaton, Rudoff & Sucharow
100 Park Avenue, 12th Floor
New York, NY 10017
Counsel for Appellant
Kathleen McDermott [ARGUED]
Blank Rome
600 New Hampshire Avenue, N.W.
Suite 1100
Washington, DC 20037
Counsel for Appellee
OPINION OF THE COURT
RENDELL, Circuit Judge.
On appeal, plaintiff R. Steven Scherfel asks that we find that West End Family
Pharmacy (“West End”), a New Jersey pharmacy which supplies drugs to Medicaid
beneficiaries, violated the False Claims Act (“FCA”), 31 U.S.C. § 3729, et seq., by failing
to credit Medicaid for returned, unused medication and submitting successive claims to
Medicaid for the repackaging and subsequent sale of such medication. Scherfel argues
that the government was charged for “worthless services” and was the recipient of false
express certifications all in violation of the FCA. He also urges that there are genuine
issues of material fact regarding the commission of these alleged violations in several
jurisdictions outside New Jersey.
Only recently, we confronted a nearly identical challenge under the False Claims
Act, and, as memorialized in Judge Roth’s thoughtful and comprehensive opinion, see
2
United States ex rel. Quinn v. Omnicare, Inc., No. 03-2187,
2004 U.S. App. LEXIS
18474, at *1 (3d Cir. Sept. 1, 2004), concluded there was no liability for a New Jersey
pharmacy engaging in the practices alleged. We find Omnicare to be controlling.1
Here, the Bankruptcy Court considering Scherfel’s claims determined he failed to
raise a genuine issue of material fact and granted summary judgment to debtors Genesis
Health Ventures, Inc. (“Genesis”) and NeighborCare Pharmacy Services, Inc.
(“NeighborCare”),2 estimating Scherfel’s proof of claim stemming from his False Claims
Act qui tam lawsuit at zero. The District Court affirmed the Bankruptcy Court’s order
and adopted its opinion.3 For the reasons set forth below, we will affirm.
1
Despite Appellant’s strident, but somewhat convoluted, efforts to distinguish the
instant case from Omnicare, that decision squarely addresses his contentions on appeal.
We recognize that the court in Omnicare discussed theories of liability under the FCA
presented in a slightly different manner than those advanced by Scherfel; however,
Appellant’s legal theories, albeit creatively framed, comprise the exact same behavior and
practices complained of by plaintiff in Omnicare.
2
The pharmacy at issue in this action, West End, was owned by Vitalink Pharmacy
Services, Inc. (“Vitalink”) until 1998, at which time Genesis subsidiary NeighborCare
acquired West End through a merger involving Genesis and Vitalink.
3
The Bankruptcy Court for the District of Delaware had jurisdiction pursuant to 28
U.S.C. § 157(b). The District Court for the District of Delaware had jurisdiction to hear
the appeal of the Bankruptcy Court’s order pursuant to 28 U.S.C. § 158(a). We have
jurisdiction over the District Court’s order pursuant to 28 U.S.C. § 158(d).
Because the District Court sat as an appellate court, our review is plenary and we
apply the same standards it applied. Stonington Partners, Inc. v. Lernout & Hauspie
Speech Prod. N.V.,
310 F.3d 118, 121 (3d Cir. 2002). Thus, we review the Bankruptcy
Court’s legal determinations de novo, its factual findings for clear error, and its exercises
of discretion for abuse of discretion.
Id. at 121-22.
3
I.
Medicaid is a federal program designed to provide health care services to
qualifying low income individuals not subject to any other coverage. 42 U.S.C. § 1396, et
seq. Though jointly financed and regulated by the federal and state governments, each
state bears responsibility for administration of services. In New Jersey, the responsible
agency is the Division of Medical Assistance and Health Services (“DMAHS”).
In furtherance of this administration of services under Medicaid, a state agency
like DMAHS enters into agreements with participating health care providers whereby
providers submit claim forms to receive reimbursements. In New Jersey, DMAHS has set
forth instructions for filing claims in a manual titled Pharmacy Services Fiscal Agent
Billing Supplement (“FABS”); therein, pharmacies are directed to submit claims to
Medicaid using the MC-6 claim form. The MC-6 claim form contains a “Provider
Certification” requiring signature and which states in part: “I certify that . . . no part of the
net amount payable under this claim has been paid . . . .”
Appellant Scherfel owns the Cherry Hill Convalescent Center (“CHCC”), a
nursing home in Cherry Hill, New Jersey. Approximately seventy percent of the home’s
residents are covered by Medicaid, and from 1987 to December 31, 1996, CHCC
contracted with West End, a Medicaid participant, to provide pharmacy services to
CHCC’s residents.
West End fulfilled its obligation by maintaining a fleet of “pharmaceutical carts” at
4
the nursing home itself. West End would stock the carts with whatever pharmaceuticals
residents required – most came in small bottles or “bingo cards” – and the CHCC staff
would then dispense the drugs. When restocking the carts, West End routinely collected
any unused pharmaceuticals; according to Scherfel, in an average month, the pharmacy
collected between 700 and 7000 unused pills initially sold to residents covered by
Medicaid. Following collection, Scherfel alleges, it was West End’s practice to
repackage and resell the unused pills without crediting Medicaid for the sums already
paid out to cover the cost of the pills, and to then submit “duplicative” claims to Medicaid
for the subsequent resale of the pills to a new patient.
In support of his allegations, Scherfel offers only the following evidence: 1) a
December 1996 statement by West End’s Regional Vice President Sam Veltri (in
response to an inquiry by Scherfel) indicating that W est End “provides no credits to
Medicaid” for unused medications, justified on the ground that “no one in the industry”
provides such credits because the Medicaid reimbursement rates are “too low”; and 2)
evidence of sporadic credit payments (or lack of payments) to several states other than
New Jersey over a span of years, based upon which Scherfel argues that West End must
have been evading its responsibilities since it paid out less than $400,000 over a seven
year period and more than $2,000,000 during 2001, after his qui tam suit was filed.
Federal regulations contain no provisions requiring pharmaceutical providers to
collect or account for unused drugs, regulating the handling of such drugs if collected, or
5
demanding credits be given to Medicaid for such drugs.4 However, state agencies
charged with administering the Medicaid program have promulgated various regulations,
some require that returned drugs be destroyed, while others demand destruction of only
specific types of medication. Some states direct pharmaceutical providers to credit the
state Medicaid program for any returned and reusable drugs, while others do not. Though
New Jersey requires the destruction of certain types of drugs, see N.J.A.C. 13:39-9.15, it
does not mandate that Medicaid be credited for the return of unused pharmaceuticals.5
II.
Scherfel’s essential claim is that the government was made to pay twice for the
same medication – he argues that W est End’s “duplicative” claim forms not only
contained express false certifications stating “no part of the net amount payable under this
claim has been paid,” but also that their submission constituted claims for “worthless
services” in violation of the FCA.
4
A 1985 memorandum from the Office of the Inspector General for the Department of
Health and Human Services explained: “Medicaid regulations governing reimbursement
for drugs are specified in 42 C.F.R. 447.331 through 447.334. Those regulations,
however, are silent regarding recovery by pharmacies for reusable drugs. They do not
require that reusable drugs be recovered by pharmacies nor appropriate credits be made to
Medicaid if the drugs are recovered.” (A146.)
5
In a letter concerning another qui tam action dated December 14, 1998, DMAHS’s
Assistant Director of the Office of Health Service Administration stated, “DMAHS does
not regulate the crediting or return of unused medications dispensed to nursing facility
beneficiaries” and that he was “unaware of federal and State regulations requiring that
any unused pharmaceuticals be properly credited to Medicaid.” (A149.)
6
Regarding the latter contention, though Scherfel clearly urges that “worthless
services” encompasses a broader spectrum of behavior than his false certification theory,
the concept itself simply does not cover the alleged practice at issue. Case law in the area
of “worthless services” under the FCA addresses instances in which either services
literally are not provided or the service is so substandard as to be tantamount to no
service at all. See, e.g., United States ex rel. Lee v. Smithkline Beecham, Inc.,
245 F.3d
1048, 1053 (9th Cir. 2001) (construing complaint alleging submission of falsified medical
test results for reimbursement to Medicaid as a theory based on “worthless services
fraudulently provided to the government”). Moreover, as noted by the court in United
States ex rel. Mikes v. Strauss,
274 F.3d 687, 702 (2d Cir. 2001), “An allegation that
defendants violated the Act by submitting claims for worthless services is not predicated
upon the false certification theory.” Here, Scherfel’s worthless services theory is
indistinguishable from his alternatively advanced false certification theory – under both,
he contends the government was duped into paying twice for the same drugs and that
West End made misrepresentations in order to procure such payment.
Like the plaintiff in Omnicare, Scherfel argues that, when a returned medication is
resold, West End is making a claim for an amount that has, at least in part, already been
paid.
2004 U.S. App. LEXIS 18474, at *17. The MC-6 form requires West End to
certify that “no part of the net amount payable under this claim has been paid,” and
Scherfel asserts that West End’s agreement constitutes an expressly false certification
7
because the medication has been sold for a second time and West End in turn seeks to be
paid a second time. But, in so arguing, Scherfel ignores the relevant legal scheme of state
and federal law. In Omnicare, this contention was expressly addressed:
[E]ven assuming that [defendant] is submitting successive claims for the same
medications, there can be no FCA liability because New Jersey regulations
entitle [defendant] to recycle and redispense returned medications. Section
13:39-9.15(a)(2) of the New Jersey Administrative Code, entitled “Disposal
of unused medications,” allows unused unit dose packaged medication, that
“has been stored in a medication room or secure area in the institution . . .
[with the] seal and control number . . . intact” to be “recycled and
redispensed.” The regulation does not, however, require pharmacies to credit
Medicaid for the “recycled and redispensed” medications. Because
[defendant] can legally recycle returned medications, the initial sale and the
subsequent sale of a returned medication are properly viewed as separate
transactions. As the District Court held, these transactions are “not duplicative
in any sense that would make them inconsistent with the full-payment
representation on the MC-6.” Under this separate transaction theory,
[defendant] does not make a false representation on the second claim form
even though it does not state that Medicaid has already paid, at least in part,
for a redispensed medication.
In so concluding, we recognize that the second claim would be submitted to
Medicaid for payment for the same medication. When [defendant] submits
the second claim, it knows that the medication, which is the subject of that
claim, was already dispensed once and returned. . . . However, because New
Jersey regulations allow [defendant] to recycle returned medications and
because no regulation requires . . . Medicaid pharmacies to credit Medicaid for
the returns, we conclude that we cannot impose FCA liability based on the
submission of the second claim.
Id. at *21-23 (record citation omitted). Therefore, even if Scherfel could adduce proof
of successive billing, based on a separate transaction theory, such billing, Omnicare
8
holds, is not tantamount to duplicative billing violative of applicable law.6
Finally, Scherfel argues that genuine issues of material fact exist with respect to
whether FCA violations were committed against the federal Medicaid programs operating
in several states other than New Jersey. He bases his allegations on the statements made
by Sam Veltri at the December 1996 meeting, and Vitalink’s record of payment of credits
in other jurisdictions. With respect to the former, Scherfel claims that when Veltri stated
to Scherfel that no credits were being afforded to Medicaid for returned drugs, it should be
inferred that Veltri was speaking about Vitalink’s nationwide policy. With respect to the
latter, Scherfel argues that from Vitalink and Genesis’ crediting history – as evidenced by
the discovery of payments to only two states over a seven year period – it should be
inferred that Appellees failed to credit properly refunds to several other states.
But, as noted in Omnicare, “a False Claims Act plaintiff cannot ‘merely . . .
describe a private scheme in detail but then . . . allege simply and without any stated
reason for his belief that claims requesting illegal payments must have been submitted,
were likely submitted or should have been submitted to the Government.’” 2004 U.S.
App. LEXIS 18474, at *19 (quoting United States ex rel. Clausen v. Lab. Corp. of Am.,
6
In his supplemental letter brief, Scherfel seeks to distinguish Omnicare from Genesis
based on the fact that defendants in Omnicare paid out 50% of the credits owed to
Medicare, as opposed to the zero percent he alleges West End conceded in Sam Veltri’s
comment. However, this distinction is not viable under Omnicare. Even if
NeighborCare and Genesis altogether failed to credit Medicaid for returned
pharmaceuticals and even if those returned drugs were repackaged, resold, and rebilled to
Medicaid, New Jersey regulations do not prohibit the practice.
9
290 F.3d 1301, 1311 (11th Cir. 2002)). Proof of the filing of such claims is required.
Id.
None of the evidence offered by Scherfel suffices to create a genuine issue of material fact
as to whether the defendants did or did not issue required credits outside of New Jersey or,
equally important, which states, if any, regulate claims in connection with the return and
resale of unused drugs. Perhaps most significantly, Scherfel offers no evidence to show
that drugs actually were returned and resold, and that Medicaid was not thereafter properly
credited.
This lack of evidence as to the fact pattern, and specific instances in other
jurisdictions, is symptomatic of the problem underlying Scherfel’s allegations in general –
they are just that, mere allegations. As was the case with the qui tam plaintiff in
Omnicare, Scherfel has failed to adduce evidence of any actual filing of a false claim.
III.
In the absence of any statute or regulation requiring health care providers in New
Jersey to credit Medicaid for returned drugs, we conclude that neither W est End’s failure
to do so, nor its alleged practice of successive billing based on a separate transaction
theory, gives rise to a False Claims Act violation. As for the jurisdictions that do require
such credits, Scherfel has not provided any evidence that defendants failed to issue such
credits as were required. Accordingly, we will AFFIRM the order of the District Court.
10