Ehigiator O. Akhigbe: Debarment Order, 79005-79006 [2010-31776]
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Federal Register / Vol. 75, No. 242 / Friday, December 17, 2010 / Notices
Dated: December 13, 2010.
Leslie Kux,
Acting Assistant Commissioner for Policy.
[FR Doc. 2010–31693 Filed 12–16–10; 8:45 am]
BILLING CODE 4160–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2010–N–0235]
Ehigiator O. Akhigbe: Debarment
Order
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
The Food and Drug
Administration (FDA) is issuing an
order under the Federal Food, Drug, and
Cosmetic Act (the FD&C Act) debarring
Ehigiator O. Akhigbe, MD for 25 years
from providing services in any capacity
to a person that has an approved or
pending drug product application. We
base this order on a finding that Dr.
Akhigbe was convicted of 17 felonies for
conduct involving fraud, false statement
and falsification or destruction of
records. Dr. Akhigbe was given notice of
the proposed debarment and an
opportunity to request a hearing within
the timeframe prescribed by regulation.
Dr. Akhigbe failed to respond. Dr.
Akhigbe’s failure to respond constitutes
a waiver of his right to a hearing
concerning this action.
DATES: This Order is effective December
17, 2010.
ADDRESSES: Submit applications for
termination of debarment to the
Division of Dockets Management (HFA–
305), Food and Drug Administration,
5630 Fishers Lane, rm. 1061, Rockville,
MD 20852.
FOR FURTHER INFORMATION CONTACT:
Kenny Shade, Office of Regulatory
Affairs, Food and Drug Administration,
5600 Fishers Lane, Rockville, MD
20857, 240–632–6844.
SUPPLEMENTARY INFORMATION:
SUMMARY:
emcdonald on DSK2BSOYB1PROD with NOTICES
I. Background
Section 306(b)(2)(B)(ii)(I) of the FD&C
Act (21 U.S.C. 335a(b)(2)(B)(ii)(I))
permits FDA to debar an individual if it
finds that the individual has been
convicted of a felony which involves
bribery, payment of illegal gratuities,
fraud, perjury, false statement,
racketeering, blackmail, extortion,
falsification or destruction of records, or
interference with, obstruction of an
investigation into, or prosecution of, any
criminal offense, and it finds, on the
VerDate Mar<15>2010
16:45 Dec 16, 2010
Jkt 223001
basis of the conviction and other
information, that such individual has
demonstrated a pattern of conduct
sufficient to find that there is reason to
believe that individual may violate
requirements under the Act relating to
drug products.
On March 19, 2010, the United States
District Court for the District of
Columbia entered judgment against Dr.
Akhigbe for one count of health care
fraud in violation of 18 U.S.C. 1347, and
16 counts of false statements in health
care matters in violation of 18 U.S.C.
1035.
FDA’s finding that debarment is
appropriate is based on the felony
convictions referenced herein. The
factual basis for those convictions is as
follows: Dr. Akhigbe was a medical
doctor with licenses to practice in the
District of Columbia, Maryland,
Pennsylvania, and Virginia. The District
of Columbia Medicaid Program
contracted with Amerigroup Corp.
(Amerigroup) to act as its fiscal agent for
the processing and payment of claims
submitted by Medicaid providers. On or
about December 6, 2001, Dr. Akhigbe
entered into a Participating Physician
Agreement with Amerigroup whereby
he agreed to provide healthcare services
to District of Columbia Medicaid
beneficiaries.
Dr. Akhigbe prepared and submitted
his own billing to Amerigroup for
medical services he purportedly
provided to his patients. For each billed
visit, Dr. Akhigbe or others acting at his
direction, generated insurance claim
forms which included his certification
that all of the information on the claim
forms was accurate. From on or about
December 6, 2001, until the termination
of his contract with Amerigroup on June
24, 2004, Dr. Akhigbe submitted
approximately 3,957 claims to
Amerigroup for services he purportedly
provided to Medicaid patients and
sought approximately $807,347.00 from
Amerigroup.
Beginning in approximately December
2002, and continuing to approximately
May 2005, in the District of Columbia
and elsewhere, Dr. Akhigbe knowingly,
willfully, and with intent to defraud,
executed a scheme and artifice to
defraud Amerigroup as to material
matters in connection with the delivery
of any payment for health care benefits,
items, and services, and to obtain
money from Amerigroup by means of
material false and fraudulent pretenses
and representations and the
concealment of material facts in
connection with the delivery of and
payment for health care benefits, items,
and services. As part of his scheme, Dr.
Akhigbe repeatedly prepared and
PO 00000
Frm 00041
Fmt 4703
Sfmt 4703
79005
submitted false claims in which he
purported to have performed surgical or
invasive medical procedures on District
of Columbia Medicaid patients that
were never performed, he billed for
office visits that never occurred, and he
continued to bill for a period of time
after a minor or major procedure during
which no additional bills could be
submitted. In order to conceal from
Amerigroup that he was billing for
procedures that he had not performed,
Dr. Akhigbe created false progress notes
indicating the dates, times and medical
procedures that he claimed to have
performed and inserted the false
progress notes into his patients’ medical
files to corroborate a number of false
claims.
As a result of his convictions, on
September 13, 2010, FDA sent Dr.
Akhigbe a notice by certified mail
proposing to debar him for 25 years
from providing services in any capacity
to a person that has an approved or
pending drug product application. The
proposal was based on a finding, under
section 306(b)(2)(B)(ii)(I) of the FD&C
Act (21 U.S.C. 335a(b)(2)(B)(ii)(I)), that
Dr. Akhigbe was convicted of felonies
for conduct involving fraud, false
statement and falsification or
destruction of records and that Dr.
Akhigbe has demonstrated a pattern of
conduct sufficient to find that there is
reason to believe that individual may
violate requirements under the FD&C
Act relating to drug products. The
proposal also offered Dr. Akhigbe an
opportunity to request a hearing,
providing him 30 days from the date of
receipt of the letter in which to file the
request, and advised him that failure to
request a hearing constituted a waiver of
the opportunity for a hearing and of any
contentions concerning this action. Dr.
Akhigbe failed to respond within the
timeframe prescribed by regulation and
has, therefore, waived his opportunity
for a hearing and waived any
contentions concerning his debarment
(21 CFR part 12).
II. Findings and Order
Therefore, the Director, Office of
Enforcement, Office of Regulatory
Affairs, under Section 306(b)(2)(B)(ii)(I)
of the FD&C Act (21 U.S.C.
335a(b)(2)(B)(ii)(I)) under authority
delegated to him (Staff Manual Guide
1410.35), finds that Ehigiator O.
Akhigbe has been convicted of felonies
for conduct involving fraud, false
statement and falsification or
destruction of records.
As a result of the foregoing finding,
Dr. Akhigbe is debarred for 25 years
from providing services in any capacity
to a person with an approved or
E:\FR\FM\17DEN1.SGM
17DEN1
79006
Federal Register / Vol. 75, No. 242 / Friday, December 17, 2010 / Notices
pending drug product application under
sections 505, 512, or 802 of the FD&C
Act (21 U.S.C. 355, 360b, or 382), or
under section 351 of the Public Health
Service Act (42 U.S.C. 262), effective
(see DATES), (see section 306(c)(1)(B),
(c)(2)(A)(iii), and 201(dd) of the FD&C
Act (21 U.S.C. 335a(c)(1)(B),
(c)(2)(A)(iii), and 321(dd))). Any person
with an approved or pending drug
product application who knowingly
employs or retains as a consultant or
contractor, or otherwise uses the
services of Dr. Akhigbe, in any capacity
during Dr. Akhigbe’s debarment, will be
subject to civil money penalties (section
307(a)(6) of the FD&C Act (21 U.S.C.
335b(a)(6))). If Dr. Akhigbe provides
services in any capacity to a person with
an approved or pending drug product
application during his period of
debarment he will be subject to civil
money penalties (section 307(a)(7) of the
FD&C Act). In addition, FDA will not
accept or review any abbreviated new
drug applications submitted by or with
the assistance of Dr. Akhigbe during his
period of debarment (section
306(c)(1)(B) of the FD&C Act (21 U.S.C.
335a(c)(1)(B)).
Any application by Dr. Akhigbe for
termination of debarment under section
306(d)(4) of the FD&C Act should be
identified with Docket No. FDA–2010–
N–0235 and sent to the Division of
Dockets Management (see ADDRESSES).
All such submissions are to be filed in
four copies. The public availability of
information in these submissions is
governed by 21 CFR 10.20(j).
Publicly available submissions may
be seen in the Division of Dockets
Management between 9 a.m. and 4 p.m.,
Monday through Friday.
Dated: November 19, 2010.
Howard R. Sklamberg,
Director, Office of Enforcement, Office of
Regulatory Affairs.
Dates and Times: January 19, 2011,
8:30 a.m.–4 p.m., January 20, 2011, 8:30
a.m.–12:15 p.m.
Place: Hilton Washington DC/
Rockville Executive Meeting Center,
1750 Rockville Pike, Rockville, MD
20852. Telephone: (301) 468–1100.
Status: The meeting will be open to
the public.
Agenda: On the morning of January
19, following welcoming remarks from
the COGME Chair, HRSA senior
management, and the Executive
Secretary of COGME, there will be an
introduction of COGME members.
The rest of the first day will consist
of presentations covering various
aspects of graduate medical education,
Bureau of Health Professions activities
concerning health workforce issues, a
study of primary care physician
projections by state, and work of the
Medicare Payment and Advisory
Commission on GME issues.
On January 20, there will be
presentations on the findings and
recommendations of COGME’s 20th
report, Advancing Primary Care (cover
date December 2010). It is expected that
the rest of the morning will be taken up
in discussions in exploring the topic for
COGME’s next report.
Agenda items are subject to change as
priorities dictate.
FOR FURTHER INFORMATION CONTACT:
Anyone interested in obtaining a roster
of members or other relevant
information should write or contact
Jerald M. Katzoff, Executive Secretary,
COGME, Division of Medicine and
Dentistry, Bureau of Health Professions,
Parklawn Building, Room 9A–27, 5600
Fishers Lane, Rockville, Maryland
20857, Telephone (301) 443–4443. The
Web address for information on the
Council and the January 19–20, 2011
meeting agenda is https://cogme.gov.
Dated: December 9, 2010.
Robert Hendricks,
Director, Division of Policy and Information
Coordination.
[FR Doc. 2010–31776 Filed 12–16–10; 8:45 am]
BILLING CODE 4160–01–P
[FR Doc. 2010–31712 Filed 12–16–10; 8:45 am]
BILLING CODE 4165–15–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
emcdonald on DSK2BSOYB1PROD with NOTICES
Health Resources and Services
Administration
National Institutes of Health
Council on Graduate Medical
Education; Notice of Meeting
In accordance with section 10(a)(2) of
the Federal Advisory Committee Act
(Pub. L. 92–463), notice is hereby given
of the following meeting:
Name: Council on Graduate Medical
Education (COGME).
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16:45 Dec 16, 2010
Jkt 223001
Submission for OMB Review;
Comment Request; TransfusionTransmitted Retrovirus and Hepatitis
Virus Rates and Risk Factors:
Improving the Safety of the U.S. Blood
Supply Through Hemovigilance
Summary: Under the provisions of
Section 3507(a)(1)(D) of the Paperwork
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Frm 00042
Fmt 4703
Sfmt 4703
Reduction Act of 1995, the National
Heart, Lung, and Blood Institute
(NHLBI), the National Institutes of
Health (NIH) has submitted to the Office
of Management and Budget (OMB) a
request to review and approve the
information collection listed below.
This proposed information collection
was previously published in the Federal
Register on September 28, 2010,
Volume 75, No. 187, pages 59724–59725
and allowed 60 days for public
comment. The purpose of this notice is
to allow an additional 30 days for public
comment. The National Institutes of
Health may not conduct or sponsor, and
the respondent is not required to
respond to, an information collection
that has been extended, revised, or
implemented on or after October 1,
1995, unless it displays a current valid
OMB control number.
Proposed Collection: Title:
Transfusion-transmitted retrovirus and
hepatitis virus rates and risk factors:
Improving the safety of the U.S. blood
supply through hemovigilance. Type of
Information Collection Request: NEW.
Need and Use of Information Collection:
Information on current risk factors in
blood donors as assessed using
analytical study designs is largely
unavailable in the U.S. Studies of risk
factor profiles among HIV-infected
donors were funded by the CDC for
approximately 10 years after
implementation of serologic screening
in the mid-1980s, whereas studies of
HTLV- and HCV-seropositive (and
indeterminate) donors, funded by NIH,
were conducted in the early 1990s, but
unfortunately, none of these studies is
ongoing. Infection trend analyses have
been conducted by the American Red
Cross (ARC). The findings show
continued HIV risk with the prevalence
of HIV in first time donors hovering
around 10 per 100,000 donations in
each of the last 10 years and the
incidence in repeat donors increasing
from 1.49 per 100,000 person-years in
1999–2000 to 2.16 per 100,000 personsyears in 2007–2008. While the
prevalence of HCV in first time donors
decreased over this time interval from
345 to 163 per 100,000 donations, the
incidence in repeat donors did not
decrease and evidence of incident
infection in first time donors increased.
Moreover specific age, gender and race/
ethnicity groups were over-represented.
Significantly increased incidence of
both HIV and HCV were observed in
2007/2008 compared to 2005/2006.
Similar analyses for HBV have shown
an incidence in all donors of 3.4 per
100,000 person-years which is lower
E:\FR\FM\17DEN1.SGM
17DEN1
Agencies
[Federal Register Volume 75, Number 242 (Friday, December 17, 2010)]
[Notices]
[Pages 79005-79006]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-31776]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA-2010-N-0235]
Ehigiator O. Akhigbe: Debarment Order
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The Food and Drug Administration (FDA) is issuing an order
under the Federal Food, Drug, and Cosmetic Act (the FD&C Act) debarring
Ehigiator O. Akhigbe, MD for 25 years from providing services in any
capacity to a person that has an approved or pending drug product
application. We base this order on a finding that Dr. Akhigbe was
convicted of 17 felonies for conduct involving fraud, false statement
and falsification or destruction of records. Dr. Akhigbe was given
notice of the proposed debarment and an opportunity to request a
hearing within the timeframe prescribed by regulation. Dr. Akhigbe
failed to respond. Dr. Akhigbe's failure to respond constitutes a
waiver of his right to a hearing concerning this action.
DATES: This Order is effective December 17, 2010.
ADDRESSES: Submit applications for termination of debarment to the
Division of Dockets Management (HFA-305), Food and Drug Administration,
5630 Fishers Lane, rm. 1061, Rockville, MD 20852.
FOR FURTHER INFORMATION CONTACT: Kenny Shade, Office of Regulatory
Affairs, Food and Drug Administration, 5600 Fishers Lane, Rockville, MD
20857, 240-632-6844.
SUPPLEMENTARY INFORMATION:
I. Background
Section 306(b)(2)(B)(ii)(I) of the FD&C Act (21 U.S.C.
335a(b)(2)(B)(ii)(I)) permits FDA to debar an individual if it finds
that the individual has been convicted of a felony which involves
bribery, payment of illegal gratuities, fraud, perjury, false
statement, racketeering, blackmail, extortion, falsification or
destruction of records, or interference with, obstruction of an
investigation into, or prosecution of, any criminal offense, and it
finds, on the basis of the conviction and other information, that such
individual has demonstrated a pattern of conduct sufficient to find
that there is reason to believe that individual may violate
requirements under the Act relating to drug products.
On March 19, 2010, the United States District Court for the
District of Columbia entered judgment against Dr. Akhigbe for one count
of health care fraud in violation of 18 U.S.C. 1347, and 16 counts of
false statements in health care matters in violation of 18 U.S.C. 1035.
FDA's finding that debarment is appropriate is based on the felony
convictions referenced herein. The factual basis for those convictions
is as follows: Dr. Akhigbe was a medical doctor with licenses to
practice in the District of Columbia, Maryland, Pennsylvania, and
Virginia. The District of Columbia Medicaid Program contracted with
Amerigroup Corp. (Amerigroup) to act as its fiscal agent for the
processing and payment of claims submitted by Medicaid providers. On or
about December 6, 2001, Dr. Akhigbe entered into a Participating
Physician Agreement with Amerigroup whereby he agreed to provide
healthcare services to District of Columbia Medicaid beneficiaries.
Dr. Akhigbe prepared and submitted his own billing to Amerigroup
for medical services he purportedly provided to his patients. For each
billed visit, Dr. Akhigbe or others acting at his direction, generated
insurance claim forms which included his certification that all of the
information on the claim forms was accurate. From on or about December
6, 2001, until the termination of his contract with Amerigroup on June
24, 2004, Dr. Akhigbe submitted approximately 3,957 claims to
Amerigroup for services he purportedly provided to Medicaid patients
and sought approximately $807,347.00 from Amerigroup.
Beginning in approximately December 2002, and continuing to
approximately May 2005, in the District of Columbia and elsewhere, Dr.
Akhigbe knowingly, willfully, and with intent to defraud, executed a
scheme and artifice to defraud Amerigroup as to material matters in
connection with the delivery of any payment for health care benefits,
items, and services, and to obtain money from Amerigroup by means of
material false and fraudulent pretenses and representations and the
concealment of material facts in connection with the delivery of and
payment for health care benefits, items, and services. As part of his
scheme, Dr. Akhigbe repeatedly prepared and submitted false claims in
which he purported to have performed surgical or invasive medical
procedures on District of Columbia Medicaid patients that were never
performed, he billed for office visits that never occurred, and he
continued to bill for a period of time after a minor or major procedure
during which no additional bills could be submitted. In order to
conceal from Amerigroup that he was billing for procedures that he had
not performed, Dr. Akhigbe created false progress notes indicating the
dates, times and medical procedures that he claimed to have performed
and inserted the false progress notes into his patients' medical files
to corroborate a number of false claims.
As a result of his convictions, on September 13, 2010, FDA sent Dr.
Akhigbe a notice by certified mail proposing to debar him for 25 years
from providing services in any capacity to a person that has an
approved or pending drug product application. The proposal was based on
a finding, under section 306(b)(2)(B)(ii)(I) of the FD&C Act (21 U.S.C.
335a(b)(2)(B)(ii)(I)), that Dr. Akhigbe was convicted of felonies for
conduct involving fraud, false statement and falsification or
destruction of records and that Dr. Akhigbe has demonstrated a pattern
of conduct sufficient to find that there is reason to believe that
individual may violate requirements under the FD&C Act relating to drug
products. The proposal also offered Dr. Akhigbe an opportunity to
request a hearing, providing him 30 days from the date of receipt of
the letter in which to file the request, and advised him that failure
to request a hearing constituted a waiver of the opportunity for a
hearing and of any contentions concerning this action. Dr. Akhigbe
failed to respond within the timeframe prescribed by regulation and
has, therefore, waived his opportunity for a hearing and waived any
contentions concerning his debarment (21 CFR part 12).
II. Findings and Order
Therefore, the Director, Office of Enforcement, Office of
Regulatory Affairs, under Section 306(b)(2)(B)(ii)(I) of the FD&C Act
(21 U.S.C. 335a(b)(2)(B)(ii)(I)) under authority delegated to him
(Staff Manual Guide 1410.35), finds that Ehigiator O. Akhigbe has been
convicted of felonies for conduct involving fraud, false statement and
falsification or destruction of records.
As a result of the foregoing finding, Dr. Akhigbe is debarred for
25 years from providing services in any capacity to a person with an
approved or
[[Page 79006]]
pending drug product application under sections 505, 512, or 802 of the
FD&C Act (21 U.S.C. 355, 360b, or 382), or under section 351 of the
Public Health Service Act (42 U.S.C. 262), effective (see DATES), (see
section 306(c)(1)(B), (c)(2)(A)(iii), and 201(dd) of the FD&C Act (21
U.S.C. 335a(c)(1)(B), (c)(2)(A)(iii), and 321(dd))). Any person with an
approved or pending drug product application who knowingly employs or
retains as a consultant or contractor, or otherwise uses the services
of Dr. Akhigbe, in any capacity during Dr. Akhigbe's debarment, will be
subject to civil money penalties (section 307(a)(6) of the FD&C Act (21
U.S.C. 335b(a)(6))). If Dr. Akhigbe provides services in any capacity
to a person with an approved or pending drug product application during
his period of debarment he will be subject to civil money penalties
(section 307(a)(7) of the FD&C Act). In addition, FDA will not accept
or review any abbreviated new drug applications submitted by or with
the assistance of Dr. Akhigbe during his period of debarment (section
306(c)(1)(B) of the FD&C Act (21 U.S.C. 335a(c)(1)(B)).
Any application by Dr. Akhigbe for termination of debarment under
section 306(d)(4) of the FD&C Act should be identified with Docket No.
FDA-2010-N-0235 and sent to the Division of Dockets Management (see
ADDRESSES). All such submissions are to be filed in four copies. The
public availability of information in these submissions is governed by
21 CFR 10.20(j).
Publicly available submissions may be seen in the Division of
Dockets Management between 9 a.m. and 4 p.m., Monday through Friday.
Dated: November 19, 2010.
Howard R. Sklamberg,
Director, Office of Enforcement, Office of Regulatory Affairs.
[FR Doc. 2010-31776 Filed 12-16-10; 8:45 am]
BILLING CODE 4160-01-P