Follow-Up Activities for Product-Related Injuries

Forms and Documents

Document Name	Status
Form 182 Follow-Up Activities for Product-Related Injuries-Interviews Form	Modified
Form OMB0029_2013_PCNEI NEISS Form and Instruction	New
Form 182 from 2011 Field Manual for Investigations.pdf Supplementary Document	2013-07-18
followupactivitiesFR30.pdf Supplementary Document	2013-07-18
followupactivitiesFR60.pdf Supplementary Document	2013-07-18
OMB0029_NEISS_Supporting_Statement_2013.doc Supporting Statement A	2013-07-18
PIA_National Electronic Injury Surveillance System (NEISS).pdf Supplementary Document	2010-03-31
OMB(40)MedicalExaminerCoronerReport.pdf Supplementary Document	2006-11-07
OMB(38)HealthCareProfessional.pdf Supplementary Document	2006-11-07
OMB(37)FirePoliceInsuranceInvestigator.pdf Supplementary Document	2006-11-07
OMB(35).pdf Supplementary Document	2006-11-07
OMB(34).pdf Supplementary Document	2006-11-07
OMB(33).pdf Supplementary Document	2006-11-07
OMB(32).pdf Supplementary Document	2006-11-07
OMB(31).pdf Supplementary Document	2006-11-07
OMB(30).pdf Supplementary Document	2006-11-07
OMB(29).pdf Supplementary Document	2006-11-07
OMB(28).pdf Supplementary Document	2006-11-07
OMB(27).pdf Supplementary Document	2006-11-07
OMB(25).pdf Supplementary Document	2006-11-07
OMB(26).pdf Supplementary Document	2006-11-07
OMB(24).pdf Supplementary Document	2006-11-07
OMB(23).pdf Supplementary Document	2006-11-07
OMB(22).pdf Supplementary Document	2006-11-07
OMB(21).pdf Supplementary Document	2006-11-07
OMB(20).pdf Supplementary Document	2006-11-07
OMB(19).pdf Supplementary Document	2006-11-07
OMB(18).pdf Supplementary Document	2006-11-07
OMB(17).pdf Supplementary Document	2006-11-07
OMB(16).pdf Supplementary Document	2006-11-07
OMB(15).pdf Supplementary Document	2006-11-07
OMB(14).pdf Supplementary Document	2006-11-07
OMB(13).pdf Supplementary Document	2006-11-07
OMB(12).pdf Supplementary Document	2006-11-07
OMB(11).pdf Supplementary Document	2006-11-07
OMB(10).pdf Supplementary Document	2006-11-07
OMB(9).pdf Supplementary Document	2006-11-07
OMB(8).pdf Supplementary Document	2006-11-07
OMB(7).pdf Supplementary Document	2006-11-07
OMB(6).pdf Supplementary Document	2006-11-07
OMB(5).pdf Supplementary Document	2006-11-07
OMB(4).pdf Supplementary Document	2006-11-07
OMB(3).pdf Supplementary Document	2006-11-07
OMB(1).pdf Supplementary Document	2006-11-07
OMB(2).pdf Supplementary Document	2006-11-07

IC Document Collections

IC ID	Document Title	Status
29149	Follow-Up Activities for Product-Related Injuries-Interviews Form	Modified
207798	NEISS Form and Instruction	New

ICR Details

OMB Control No: 3041-0029	ICR Reference No: 201307-3041-001
Status: Historical Active	Previous ICR Reference No: 201003-3041-005
Agency/Subagency: CPSC	Agency Tracking No:
Title: Follow-Up Activities for Product-Related Injuries
Type of Information Collection: Revision of a currently approved collection	Common Form ICR:  No
Type of Review Request: Regular
OIRA Conclusion Action: Approved without change	Conclusion Date: 09/16/2013
	Date Received in OIRA: 07/22/2013
Terms of Clearance:

	Inventory as of this Action	Requested	Previously Approved
Expiration Date	09/30/2016	36 Months From Approved	09/30/2013
Responses	404,250	0	393,952
Time Burden (Hours)	45,008	0	49,705
Cost Burden (Dollars)	0	0	1,726,390

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Abstract: Persons who have been injured in or who have witnessed safety- related incidents involving consumer products are an important source of safety information. The Commission uses information obtained from these persons and hospital emergency rooms to support activities to eliminate or reduce unreasonable risks of injury associated with consumer products.

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Authorizing Statute(s): US Code: 15 USC 2054 Name of Law: Consumer Product Safety Act
  

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:
	78 FR 26618	05/07/2013
30-day Notice:	Federal Register Citation:	Citation Date:
	78 FR 42935	07/18/2013
Did the Agency receive public comments on this ICR? No

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Number of Information Collection (IC) in this ICR: 2

IC Title	Form No.	Form Name
NEISS	OMB0029_2013_PCNEISS_Screenshots	PCNEISS
Follow-Up Activities for Product-Related Injuries-Interviews	182	Epidemiologic Investigation Report

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ICR Summary of Burden

	Total Approved	Previously Approved	Change Due to New Statute	Change Due to Agency Discretion	Change Due to Adjustment in Estimate	Change Due to Potential Violation of the PRA
Annual Number of Responses	404,250	393,952	0	10,298	0	0
Annual Time Burden (Hours)	45,008	49,705	0	-4,697	0	0
Annual Cost Burden (Dollars)	0	1,726,390	0	-1,726,390	0	0

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: Yes

Burden Reduction Due to: Miscellaneous Actions

Short Statement: The burden has been adjusted to account for the most recent data on NEISS reporting and investigations. Several forms have also been removed from this collection which are now being covered under 3041-0146, the Publicly Available Consumer Product Safety Information Database.

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Annual Cost to Federal Government: $3,300,000

Does this IC contain surveys, censuses, or employ statistical methods? No

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: 07/22/2013

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