Interagency Risk Assessment of the Public Health Impact From Foodborne Listeria monocytogenes in Some Ready-to-Eat Foods Sliced, Prepared, and/or Packaged in Retail Facilities; Request for Comments and for Scientific Data and Information; Reopening of the Comment Period, 43714 [E9-20641]
Download as PDF
43714
Federal Register / Vol. 74, No. 165 / Thursday, August 27, 2009 / Notices
I. Background
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2008–N–0658]
Interagency Risk Assessment of the
Public Health Impact From Foodborne
Listeria monocytogenes in Some
Ready-to-Eat Foods Sliced, Prepared,
and/or Packaged in Retail Facilities;
Request for Comments and for
Scientific Data and Information;
Reopening of the Comment Period
AGENCY:
Food and Drug Administration,
HHS.
ACTION: Notice; reopening of the
comment period.
SUMMARY: The Food and Drug
Administration (FDA) is reopening until
September 29, 2009, the comment
period for the notice published in the
Federal Register of January 21, 2009 (74
FR 3617). In that document, FDA
requested comments and scientific data
and information that would assist in the
conduct of a risk assessment of the
public health impact of foodborne
Listeria monocytogenes in some readyto-eat foods sliced, prepared, and/or
packaged in retail facilities. The risk
assessment is being conducted by FDA
in collaboration with the Food Safety
and Inspection Service (FSIS). The
agency is reopening the comment period
because FDA and FSIS held a public
meeting on June 23, 2009, to present the
background, approach, scope, and data
needs for the recently initiated
interagency risk assessment (74 FR
27276; June 9, 2009) and this additional
time will allow for public comment after
this meeting.
DATES: Submit comments and scientific
data and information by September 29,
2009.
Submit written comments
and scientific data and information to
the Division of Dockets Management
(HFA–305), Food and Drug
Administration, 5630 Fishers Lane, rm.
1061, Rockville, MD 20852. Submit
electronic comments and scientific data
and information to https://
www.regulations.gov.
mstockstill on DSKH9S0YB1PROD with NOTICES
ADDRESSES:
FOR FURTHER INFORMATION CONTACT:
Sherri Dennis, Center for Food Safety
and Applied Nutrition (HFS–005), Food
and Drug Administration, 5100 Paint
Branch Pkwy., College Park, MD 20740,
301–436–2355, e-mail:
sherri.dennis@fda.hhs.gov.
SUPPLEMENTARY INFORMATION:
VerDate Nov<24>2008
17:19 Aug 26, 2009
Jkt 217001
In the Federal Register of January 21,
2009 (74 FR 3617), FDA announced
plans to conduct a risk assessment of
the public health impact of foodborne
Listeria monocytogenes in some readyto-eat foods sliced, prepared, and/or
packaged in retail facilities. Comments
were sought on data and information in
the following areas: (1) Characteristics
of ready-to-eat food markets in the
United States; (2) characteristics of deli
departments in groceries; (3) product
contamination data; (4) factors that
influence the growth of L.
monocytogenes in cheeses, deli meats,
and deli-type salads sold by retail
facilities; (5) environmental
contamination data; (6) factors that
influence the environmental
contamination and the crosscontamination of food by L.
monocytogenes in retail facilities; (7)
identity and effectiveness of control
measures or interventions intended to
reduce levels and frequency of L.
monocytogenes in the retail
environment; and (8) any other data
related to the occurrence, growth, and
control of L. monocytogenes in retail
facilities. Interested persons were given
until April 21, 2009, to submit
comments and scientific data and
information.
On June 23, 2009, FDA and FSIS held
a public meeting to present the
background, approach, scope, and data
needs for this interagency risk
assessment (74 FR 27276; June 9, 2009).
For this reason, FDA is reopening the
comment period until September 29,
2009, to allow additional time for public
comment and submission of scientific
data and information.
II. Comments
Interested persons may submit to the
Division of Dockets Management (see
ADDRESSES) written or electronic
comments, scientific data, and
information regarding this document.
Submit a single copy of electronic
comments, scientific data, and
information to https://
www.regulations.gov or two paper
copies of any mailed comments,
scientific data, and information, except
that individuals may submit one paper
copy. Submissions are to be identified
with the docket number found in
brackets in the heading of this
document. Received comments and
scientific data and information may be
seen in the Division of Dockets
Management between 9 a.m. and 4 p.m.,
Monday through Friday.
PO 00000
Frm 00051
Fmt 4703
Sfmt 4703
Dated: August 21, 2009.
David Horowitz,
Assistant Commissioner for Policy.
[FR Doc. E9–20641 Filed 8–26–09; 8:45 am]
BILLING CODE 4160–01–S
DEPARTMENT OF THE INTERIOR
Office of Surface Mining Reclamation
and Enforcement
Notice of Proposed Information
Collection for 1029–0110
AGENCY: Office of Surface Mining
Reclamation and Enforcement, Interior.
ACTION: Notice and request for
comments.
SUMMARY: In compliance with the
Paperwork Reduction Act of 1995, the
Office of Surface Mining Reclamation
and Enforcement (OSM) is announcing
its intention to request renewed
approval for the collection of
information for two technical training
program course effectiveness evaluation
forms. This collection request has been
forwarded to the Office of Management
and Budget (OMB) for review and
approval. The information collection
request describes the nature of the
information collection and the expected
burden and cost.
DATES: OMB has up to 60 days to
approve or disapprove the information
collections but may respond after 30
days. Therefore, public comments
should be submitted to OMB by
September 28, 2009, in order to be
assured of consideration.
ADDRESSES: Submit comments to the
Office of Information and Regulatory
Affairs, Office of Management and
Budget, Attention: Department of
Interior Desk Officer, by telefax at (202)
395–5806 or via e-mail to
OIRA_Docket@omb.eop.gov. Also,
please send a copy of your comments to
the Information Collection Clearance
Officer, Office of Surface Mining
Reclamation and Enforcement, 1951
Constitution Ave., NW., Room 202–SIB,
Washington, DC 20240, or electronically
to jtrelease@osmre.gov.
FOR FURTHER INFORMATION CONTACT: To
receive a copy of the information
collection request contact John Trelease
at (202) 208–2783, or electronically at
jtrelease@osmre.gov.
The Office
of Management and Budget (OMB)
regulations at 5 CFR 1320, which
implement provisions of the Paperwork
Reduction Act of 1995 (Pub. L. 104–13),
require that interested members of the
public and affected agencies have an
SUPPLEMENTARY INFORMATION:
E:\FR\FM\27AUN1.SGM
27AUN1
Agencies
[Federal Register Volume 74, Number 165 (Thursday, August 27, 2009)]
[Notices]
[Page 43714]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E9-20641]
[[Page 43714]]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA-2008-N-0658]
Interagency Risk Assessment of the Public Health Impact From
Foodborne Listeria monocytogenes in Some Ready-to-Eat Foods Sliced,
Prepared, and/or Packaged in Retail Facilities; Request for Comments
and for Scientific Data and Information; Reopening of the Comment
Period
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice; reopening of the comment period.
-----------------------------------------------------------------------
SUMMARY: The Food and Drug Administration (FDA) is reopening until
September 29, 2009, the comment period for the notice published in the
Federal Register of January 21, 2009 (74 FR 3617). In that document,
FDA requested comments and scientific data and information that would
assist in the conduct of a risk assessment of the public health impact
of foodborne Listeria monocytogenes in some ready-to-eat foods sliced,
prepared, and/or packaged in retail facilities. The risk assessment is
being conducted by FDA in collaboration with the Food Safety and
Inspection Service (FSIS). The agency is reopening the comment period
because FDA and FSIS held a public meeting on June 23, 2009, to present
the background, approach, scope, and data needs for the recently
initiated interagency risk assessment (74 FR 27276; June 9, 2009) and
this additional time will allow for public comment after this meeting.
DATES: Submit comments and scientific data and information by September
29, 2009.
ADDRESSES: Submit written comments and scientific data and information
to the Division of Dockets Management (HFA-305), Food and Drug
Administration, 5630 Fishers Lane, rm. 1061, Rockville, MD 20852.
Submit electronic comments and scientific data and information to
https://www.regulations.gov.
FOR FURTHER INFORMATION CONTACT: Sherri Dennis, Center for Food Safety
and Applied Nutrition (HFS-005), Food and Drug Administration, 5100
Paint Branch Pkwy., College Park, MD 20740, 301-436-2355, e-mail:
sherri.dennis@fda.hhs.gov.
SUPPLEMENTARY INFORMATION:
I. Background
In the Federal Register of January 21, 2009 (74 FR 3617), FDA
announced plans to conduct a risk assessment of the public health
impact of foodborne Listeria monocytogenes in some ready-to-eat foods
sliced, prepared, and/or packaged in retail facilities. Comments were
sought on data and information in the following areas: (1)
Characteristics of ready-to-eat food markets in the United States; (2)
characteristics of deli departments in groceries; (3) product
contamination data; (4) factors that influence the growth of L.
monocytogenes in cheeses, deli meats, and deli-type salads sold by
retail facilities; (5) environmental contamination data; (6) factors
that influence the environmental contamination and the cross-
contamination of food by L. monocytogenes in retail facilities; (7)
identity and effectiveness of control measures or interventions
intended to reduce levels and frequency of L. monocytogenes in the
retail environment; and (8) any other data related to the occurrence,
growth, and control of L. monocytogenes in retail facilities.
Interested persons were given until April 21, 2009, to submit comments
and scientific data and information.
On June 23, 2009, FDA and FSIS held a public meeting to present the
background, approach, scope, and data needs for this interagency risk
assessment (74 FR 27276; June 9, 2009). For this reason, FDA is
reopening the comment period until September 29, 2009, to allow
additional time for public comment and submission of scientific data
and information.
II. Comments
Interested persons may submit to the Division of Dockets Management
(see ADDRESSES) written or electronic comments, scientific data, and
information regarding this document. Submit a single copy of electronic
comments, scientific data, and information to https://www.regulations.gov or two paper copies of any mailed comments,
scientific data, and information, except that individuals may submit
one paper copy. Submissions are to be identified with the docket number
found in brackets in the heading of this document. Received comments
and scientific data and information may be seen in the Division of
Dockets Management between 9 a.m. and 4 p.m., Monday through Friday.
Dated: August 21, 2009.
David Horowitz,
Assistant Commissioner for Policy.
[FR Doc. E9-20641 Filed 8-26-09; 8:45 am]
BILLING CODE 4160-01-S