2024-19574. Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Survey on the Occurrence of Foodborne Illness Risk Factors in Selected Restaurant and Retail Foodservice Facility Types  

  • Table 1—Description of the Facility Types Included in the Survey

    Facility type Description
    Full-Service Restaurants A restaurant where customers place their orders at their tables, are served their meals at the tables, receive the services of the wait staff, and pay at the end of the meals.
    Fast-Food Restaurants A restaurant that is not a full-service restaurant. This includes restaurants commonly referred to as quick-service restaurants and fast, casual restaurants.
    Retail Food Stores Supermarkets and grocery stores that have a deli department/operation as described as follows:
    • Deli department/operation—Areas in a retail food store where foods, such as luncheon meats and cheeses, are sliced for the customers and where sandwiches and salads are prepared onsite or received from a commissary in bulk containers, portioned, and displayed. Parts of deli operations may include:
    • Salad bars, pizza stations, and other food bars managed by the deli department manager.
    • Areas where other foods are cooked or prepared and offered for sale as ready-to-eat and are managed by the deli department manager.
    Data will also be collected in the following areas of a supermarket or grocery store, if present:
    • Seafood department/operation—Areas in a retail food store where seafood is cut, prepared, stored, or displayed for sale to the consumer. In retail food stores where the seafood department is combined with another department ( e.g., meat), the data collector will only assess the procedures and practices associated with the processing of seafood.
    • Produce department/operation—Areas in a retail food store where produce is cut, prepared, stored, or displayed for sale to the consumer. A produce operation may include salad bars or juice stations that are managed by the produce manager.

    The results of this study period will be used to:

    • Develop retail food safety initiatives, policies, and targeted intervention strategies focused on controlling foodborne illness risk factors;
    • Provide technical assistance to State, local, tribal, and territorial regulatory professionals;
    • Identify FDA retail work plan priorities; and
    • Inform FDA resource allocation to enhance retail food safety nationwide.

    The objectives of this study are to:

    • Identify the least and most often occurring foodborne illness risk factors and food safety behaviors/practices in restaurants within the United States;
    • Determine the extent to which Food Safety Management Systems and the presence of a Certified Food Protection Manager impact the occurrence of foodborne illness risk factors and food safety behaviors/practices; and
    • Determine whether the occurrence of foodborne illness risk factors food safety behaviors/practices in delis differs based on an establishment's risk categorization and status as a single-unit or multiple-unit operation (e.g., restaurants that are part of an operation with two or more units).

    A geographical information system database containing a listing of businesses throughout the United States provides the establishment inventory for the data collections. FDA samples establishments from the inventory based on the descriptions in table 1. FDA does not intend to sample operations that handle only prepackaged food items or conduct low-risk food preparation activities. The “FDA Food Code” contains a grouping of establishments by risk, based on the type of food preparation that is normally conducted ( print page 70654) within the operation.[5] The intent is to sample establishments that fall under risk categories 2 through 4.

    FDA has approximately 25 Retail Food Specialists (Specialists) who serve as the data collectors for the study. A standard form is used by the Specialists during each data collection. The form is divided into three sections: Section 1—“Establishment Information”; Section 2—“Regulatory Authority Information”; and Section 3—“Foodborne Illness Risk Factor and Food Safety Management System Assessment.” The information in Section 1 “Establishment Information” of the form is obtained during an interview with the establishment owner or person in charge by the Specialist and includes a standard set of questions. The information in Section 2 “Regulatory Authority Information” is obtained during an interview with the program director of the State or local jurisdiction that has regulatory responsibility for conducting inspections for the selected establishment.

    Section 3 includes three parts: Part A for tabulating the Specialists' observations of the food employees' behaviors and practices in limiting contamination, proliferation, and survival of food safety hazards; Part B for assessing the food safety management system being implemented by the facility; and Part C for assessing the frequency and extent of food employee handwashing. The information in Part A is collected from the Specialists' direct observations of food employee behaviors and practices. Infrequent, nonstandard questions may be asked by the Specialists if clarification is needed on the food safety procedure or practice being observed. The information in Part B is collected by making direct observations and asking follow-up questions of facility management to obtain information on the extent to which the food establishment has developed and implemented food safety management systems. The information in Part C is collected by making direct observations of food employee handwashing. No questions are asked in the completion of Section 3, Part C of the form.

    FDA collects the following information associated with the establishment's identity: establishment name, street address, city, State, ZIP Code, county, industry segment, and facility type. The establishment-identifying information is collected to ensure the data collections are not duplicative. Other information related to the nature of the operation, such as seating capacity and number of employees per shift, is also collected.

    The burden associated with the completion of Sections 1 and 3 of Form FDA 3967 is specific to the persons in charge of the selected facilities. The burden includes the time it will take the person in charge to accompany the data collector during the site visit and answer the data collector's questions. The burden related to the completion of Section 2 of the form is specific to the program directors (or designated individuals) of the respective regulatory authorities. This burden includes the time it will take to answer the data collectors' questions and is the same regardless of the facility type. Data will be consolidated and reported in a manner that does not reveal the identity of any establishment included in the study.

    FDA has collaborated with the Food Protection and Defense Institute to develop a web-based platform in FoodSHIELD to collect, store, and analyze data for the Retail Risk Factor Study. This platform is accessible to State, local, territorial, and tribal regulatory jurisdictions to collect data relevant to their own risk factor studies. Data will be consolidated and reported in a manner that does not reveal the identity of any establishment included in the study.

    In the Federal Register of March 6, 2024 (89 FR 15996), FDA published a 60-day notice requesting public comment on the proposed collection of information. One comment was received. It was in favor of the study, but it was not responsive to the four collection of information topics solicited.

    FDA estimates the burden of this collection of information as follows:

    Table 2—Estimated Annual Reporting Burden 1

    Activity Number of respondents Number of responses per respondent Total annual responses Average burden per response Total hours
    Fast-Food and Full-Service Restaurants—Form FDA 3966 400 1 400 2 800
    Retail Food Stores—Form FDA 3967 400 1 400 2 800
    Entry Refusals—All Facility Types 24 1 24 0.08 (5 minutes) 2
    Total 1,602
    1  There are no capital costs of operating and maintenance costs associated with this collection of information.

Document Information

Published:
08/30/2024
Department:
Food and Drug Administration
Entry Type:
Notice
Action:
Notice.
Document Number:
2024-19574
Dates:
Submit written comments (including recommendations) on the collection of information by September 30, 2024.
Pages:
70652-70654 (3 pages)
Docket Numbers:
Docket No. FDA-2024-N-0021
PDF File:
2024-19574.pdf