United States of America v. U.S. Oncology, Inc.

CourtDistrict Court, E.D. New York
DecidedSeptember 8, 2023
Docket1:19-cv-05125
StatusUnknown

This text of United States of America v. U.S. Oncology, Inc. (United States of America v. U.S. Oncology, Inc.) is published on Counsel Stack Legal Research, covering District Court, E.D. New York primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
United States of America v. U.S. Oncology, Inc., (E.D.N.Y. 2023).

Opinion

UNITED STATES DISTRICT COURT EASTERN DISTRICT OF NEW YORK --------------------------------------------------------- x

UNITED STATES OF AMERICA, THE STATES OF CALIFORNIA, COLORADO, CONNECTICUT, DELAWARE, OPINION & ORDER DISTRICT OF COLUMBIA, FLORIDA, GEORGIA, HAWAII, ILLINOIS, 19-cv-5125 (NG) (LB) INDIANA, IOWA, LOUISIANA, MARYLAND, MASSACHUSETTS, MICHIGAN, MINNESOTA, MONTANA, NEVADA, NEW HAMPSHIRE, NEW JERSEY, NEW MEXICO, NEW YORK, NORTH CAROLINA, OKLAHOMA, RHODE ISLAND, TENNESSEE, TEXAS, VERMONT, VIRGINIA, WASHINGTON, WISCONSIN, THE CITY OF CHICAGO, AND THE CITY OF NEW YORK ex rel. OMNI HEALTHCARE INC.,

Plaintiffs, -against- U.S. ONCOLOGY, INC., Defendant. --------------------------------------------------------- x GERSHON, United States District Judge:

I. Background Relator Omni Healthcare Inc. (“Omni”) filed a qui tam action on behalf of the United States, 30 states, the District of Columbia, and the cities of New York and Chicago against U.S. Oncology, Inc. (“U.S. Oncology”), alleging violations of the False Claims Act (“FCA”), 31 U.S.C. §§ 3729 et seq., analogous state statutes, and the common law. U.S. Oncology moved to dismiss the original complaint in its entirety, under Rules 12(b)(1) and 12(b)(6) of the Federal Rules of Civil Procedure, principally arguing that the FCA’s “public disclosure bar” barred the action. I agreed and dismissed the original complaint. I rejected Omni’s argument that the public disclosure bar does not apply to an action filed against a defendant that was previously dismissed from a relator’s own prior action by reason of the first-to-file bar. Turning to the “original source” exception, I found that Omni had not established that it met the pre- or post-amendment public disclosure bar’s definition for an “original source of the information.” Familiarity with

my prior decision, including the relevant procedural history, facts as alleged in the original complaint, and my rulings regarding the public disclosure bar, is presumed. See U.S. ex rel. Omni Healthcare Inc. v. U.S. Oncology, Inc. (“U.S. Oncology I”), 2022 WL 17685383 (E.D.N.Y. July 21, 2022). Following the dismissal of the original complaint, I granted Omni’s unopposed motion for leave to file an amended complaint, and Omni filed its First Amended Complaint (the “Complaint”). The Complaint’s allegations are largely the same as those alleged in the original complaint, but Omni adds factual allegations to support an argument that it satisfies the public disclosure bar’s original source exception. U.S. Oncology now moves again to dismiss the

Complaint, under Federal Rules of Civil Procedure 12(b)(1) and 12(b)(6), arguing that Omni’s amended allegations do not establish that it meets the original source exception. For the reasons set forth below, U.S. Oncology’s motion to dismiss the Complaint is granted. II. The Complaint’s Amended Allegations The following facts are drawn from the Complaint and are assumed to be true for purposes of this motion. Below, I primarily discuss the newly alleged facts that Omni has added to the Complaint, as compared to the original complaint that it filed in this action. Relator’s principal and owner is Dr. Craig Deligdish. Dr. Deligdish served as CEO of Oncology Resource Networks, which had a strategic partnership with McKesson Corporation, the current owner of Defendant. Dr. Deligdish also served on the Executive Board of the Florida Society of Clinical Oncology and on the editorial board of Value Based Cancer Care. In these roles, Dr. Deligdish served with multiple medical directors of oncology practices within the U.S.

Oncology Network as well as other employees of U.S. Oncology. Put differently, Dr. Deligdish “regularly interfaced with and supervised employees of and medical directors of member- practices of Defendant.” Complaint ¶ 116. These individuals included oncologists Dr. Barry Berman, Dr. Linda Bosserman, and Dr. Michael Kolodziej. Dr. Berman currently practices with Florida Cancer Specialists, but previously practiced oncology with U.S. Oncology Network practice Cancer Centers of Florida. Dr. Bosseman was, for ten years, the president and managing partner of Wilshire Oncology, a member of the U.S. Oncology Network. Dr. Kolodziej practiced oncology at U.S. Oncology Network practice New York Oncology/Hematology and served as National Medical Director of the U.S. Oncology Network.

In a conversation with Dr. Kolodziej, at a meeting in Florida, Dr. Deligdish learned that U.S. Oncology kept a record of the average overfill in each different oncology medication vial because different medications contained different amounts of overfill, and documents with these overfill amounts were distributed regularly to members of the US Oncology Network between 2003 and 2014 to encourage and facilitate physicians to administer overfill to patients. Through subsequent unidentified “investigation” and “conversations” with Dr. Berman, Dr. Bosserman, Dr. Kolodziej, and “others,” Dr. Deligdish learned that U.S. Oncology advocated that its physicians utilize “overfill billing” for the Oncology Drugs administered to patients. Id. ¶ 119. “As part of his investigation,” Dr. Deligdish learned that physicians throughout the U.S. Oncology Network harvested overfill and billed government payors for it. Id. ¶ 121. Dr. Kolodziej also informed Dr. Deligdish that U.S. Oncology was aware that it was illegal to bill Medicare for overfill. Nancy Payne provided additional information to Dr. Deligdish. Dr. Deligdish learned from her that the harvesting of the overfill was done either by the pharmacists or the technicians

at each office in the U.S. Oncology Network who were either employed by U.S. Oncology or acted under its direction and that the overfill was billed to government and private payers by staff employed by U.S. Oncology. Nancy Payne is the Executive Director of Cancer Centers of Florida, which was a member of the U.S. Oncology Network from 2001-2010. The Complaint also alleges the following: On or about September 13, 2012, as required by 31 U.S.C. § 3730(b)(2), Relator voluntarily submitted prior to the filing of the initial complaint in this action a confidential written disclosure statement (subject to the attorney-client privilege) to the United States Government, containing materials, evidence, and information in its possession pertaining to the allegations contained in this Complaint. Relator also voluntarily submitted a confidential written disclosure statement and this Complaint to the District of Columbia, as well as the states and cities under whose FCAs this action is partially brought. The disclosure contained the information on which the allegations in this Complaint are based.

Id. ¶ 23.

III. Discussion A. The FCA’s Public Disclosure Bar As I noted in U.S. Oncology I, the public disclosure bar was enacted in 1986 and amended in 2010. In its original, pre-amendment form, the public disclosure bar was “jurisdictional;” if the bar applied, it divested the court of its subject matter jurisdiction over an action. Rockwell Int’l Corp. v. United States, 549 U.S. 457, 467 (2007). Post-amendment, the current version of the bar is no longer jurisdictional. Instead, it serves as a ground for dismissal, such “as an affirmative defense or in connection with [a] motion to dismiss.” U.S. ex rel. Chorches v. Am. Med.

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United States of America v. U.S. Oncology, Inc., Counsel Stack Legal Research, https://law.counselstack.com/opinion/united-states-of-america-v-us-oncology-inc-nyed-2023.