Experiment to Evaluate Risk Perceptions of Produce Growers , Food Retailers, and Consumers After a Food Recall Resulting From a Foodborne Illness Outbreak

Forms and Documents

Forms and supporting documents for this ICR

Document	Type	Status	Availability
SS Retailer Study Part B - 8-10-11 clean.doc	Supporting Statement B	Uploaded 2011-11-10	Repair queued
Retailer Study Questionnaire and Stimuli 7-27-11.doc	Supplementary Document	Uploaded 2011-11-10	Repair queued
Retailer Study Protocol - Verrill.doc	Supplementary Document	Uploaded 2011-11-10	Repair queued
SS-Retailer Study Part A Sept 16 2011.doc	Supporting Statement A	Uploaded 2011-11-10	Repair queued

IC Document Collections

Information collection document groups

IC ID	Collection	Type	Status	Form
200137	Reporting: Experiment	Other-Questionnaire Instrument	New
200136	Reporting: Pretest	Other-Questionnaire Instrument	New
200135	Reporting: Retailer Screener	Other-Questionnaire Instrument	New
200134	Reporting: Grower Screener	Other-Questionnaire Instrument	New
200133	Reporting: Consumer Panel Screener	Other-Questionnaire Instrument	New
200132	Reporting: Cognitive Interviews	Other-Questionnaire Instrument	New
200131	Reporting- Cognitive Interview Recruitment	Other-Questionnaire Instrument	New

ICR Details

OMB Control No:	ICR Reference No: 201111-0910-004
Status: Historical Inactive	Previous ICR Reference No:
Agency/Subagency: HHS/FDA	Agency Tracking No:
Title: Experiment to Evaluate Risk Perceptions of Produce Growers , Food Retailers, and Consumers After a Food Recall Resulting From a Foodborne Illness Outbreak
Type of Information Collection: New collection (Request for a new OMB Control Number)	Common Form ICR:  No
Type of Review Request: Regular
OIRA Conclusion Action: Withdrawn	Conclusion Date: 07/30/2012
	Date Received in OIRA: 11/10/2011
Terms of Clearance: In accordance with 5 CFR 1320, this ICR has been withdrawn at the request of the Agency.

table that charts list comparision

	Inventory as of this Action	Requested	Previously Approved
Expiration Date		36 Months From Approved
Responses	0	0	0
Time Burden (Hours)	0	0	0
Cost Burden (Dollars)	0	0	0

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Abstract: FDA conducts research and educational and public information programs relating to food safety pursuant to its broad statutory authority, set forth in section 903(b)(2) of the Federal Food, Drug, and Cosmetic Act (FFDCA) (21 U.S.C. 393 (b)(2), to protect the public health by ensuring that foods are "safe, wholesome, sanitary, and properly labeled," and in section 903(d)(2)(C) (21 U.S.C. 393 (d)(2)(C)), to conduct research relating to foods, drugs, cosmetics and devices in carrying out the act. This proposed collection of information will be conducted under a cooperative agreement between the Joint Institute for Food Safety and Applied Nutrition (JIFSAN) and the Center for Risk Communication Research (CRCR) at the University of Maryland. JIFSAN was established in 1996 and is a public and private partnership between FDA and the University of Maryland. The CRCR will design and administer the study. The purpose of this research is to help FDA better understand whether the magnitude and duration of the decline in commodity consumption following food recalls can be partly explained by grower and retailer speculations and projections about consumers' attitudes toward food recalls resulting from foodborne illness outbreaks. This research will be used to assess how grower, retailer, and consumer perceptions, attitudes, knowledge, and beliefs affect market recovery after a hypothetical fresh spinach recall.

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Authorizing Statute(s): US Code: 21 USC 393(d)(2)(c) Name of Law: null
   US Code: 21 USC 393(b)(2) Name of Law: null
  

Citations for New Statutory Requirements: None

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Associated Rulemaking Information
RIN:	Stage of Rulemaking:	Federal Register Citation:	Date:
	Not associated with rulemaking

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Federal Register Notices & Comments
60-day Notice:	Federal Register Citation:	Citation Date:
	76 FR 21379	04/15/2011
30-day Notice:	Federal Register Citation:	Citation Date:
	76 FR 62810	10/11/2011
Did the Agency receive public comments on this ICR? Yes

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Number of Information Collection (IC) in this ICR: 7

table that charts list of burden

IC Title	Form No.	Form Name
Reporting- Cognitive Interview Recruitment
Reporting: Cognitive Interviews
Reporting: Consumer Panel Screener
Reporting: Grower Screener
Reporting: Retailer Screener
Reporting: Pretest
Reporting: Experiment

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Burden increases because of Program Change due to Agency Discretion: Yes

Burden Increase Due to: Miscellaneous Actions

Burden decreases because of Program Change due to Agency Discretion: No

Burden Reduction Due to:

Short Statement: This is a new collection. OMB has waived republication of an additional 30 day notice.

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Annual Cost to Federal Government: $200,000

Does this IC contain surveys, censuses, or employ statistical methods? Yes Part B of Supporting Statement

Is the Supporting Statement intended to be a Privacy Impact Assessment required by the E-Government Act of 2002? No

Is this ICR related to the Affordable Care Act [Pub. L. 111-148 & 111-152]? No

Is this ICR related to the Dodd-Frank Wall Street Reform and Consumer Protection Act, [Pub. L. 111-203]? No

Is this ICR related to the American Recovery and Reinvestment Act of 2009 (ARRA)? No

Is this ICR related to the Pandemic Response? Uncollected

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Common Form ICR:  No

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On behalf of this Federal agency, I certify that the collection of information encompassed by this request complies with 5 CFR 1320.9 and the related provisions of 5 CFR 1320.8(b)(3).

The following is a summary of the topics, regarding the proposed collection of information, that the certification covers:

(a) It is necessary for the proper performance of agency functions;

(b) It avoids unnecessary duplication;

(c) It reduces burden on small entities;

(d) It uses plain, coherent, and unambiguous language that is understandable to respondents;

(e) Its implementation will be consistent and compatible with current reporting and recordkeeping practices;

(f) It indicates the retention periods for recordkeeping requirements;

(g) It informs respondents of the information called for under 5 CFR 1320.8 (b)(3) about:

(i) Why the information is being collected;

(ii) Use of information;

(iii) Burden estimate;

(iv) Nature of response (voluntary, required for a benefit, or mandatory);

(v) Nature and extent of confidentiality; and

(vi) Need to display currently valid OMB control number;

(h) It was developed by an office that has planned and allocated resources for the efficient and effective management and use of the information to be collected.

(i) It uses effective and efficient statistical survey methodology (if applicable); and

(j) It makes appropriate use of information technology.

If you are unable to certify compliance with any of these provisions, identify the item by leaving the box unchecked and explain the reason in the Supporting Statement.

Certification Date: 11/10/2011

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