MEDICAL DEVICE RECALL COST SURVEY

Forms and Documents

Document Name	Status

No forms / supporting documents in this ICR. Check IC Document Collections.

IC Document Collections

IC ID	Document Title	Status
109999	MEDICAL DEVICE RECALL COST SURVEY	Migrated

ICR Details

OMB Control No: 0910-0293	ICR Reference No: 199307-0910-004
Status: Historical Active	Previous ICR Reference No:
Agency/Subagency: HHS/FDA	Agency Tracking No:
Title: MEDICAL DEVICE RECALL COST SURVEY
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: Approved without change	Conclusion Date: 10/20/1993
	Date Received in OIRA: 07/19/1993
Terms of Clearance: This information collection request is approved under the following conditions: 1) Consistent with the Oct. 20, 1993 letter from ERG Inc. to FDA, the expensive recalls (>$25 M) will not be excluded, but studi separately; 2) Any finding from the two studies must be presented in combination; and, 3) To combine these two studies FDA must have a full understanding of the frequency and distribution of both sets of recall If FDA cannot obtain adequate information on the frequency and distri- bution, the limitations of the findings will be noted whenever the results are reported.

	Inventory as of this Action	Requested	Previously Approved
Expiration Date	12/31/1993	12/31/1993
Responses	264	0	0
Time Burden (Hours)	178	0	0
Cost Burden (Dollars)	0	0	0

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Abstract: TO ASSESS INDUSTRY BENEFITS FROM FDA REGULATIONS ASSOCIATED WITH THE SAFE MEDICAL DEVICES ACT, THE COST OF MEDICAL DEVICE PRODUCT RECALLS I NEEDED. A RANDOM SURVEY OF DEVICE MANUFACTURERS THAT HAVE RECENTLY CONDUCTED PRODUCT RECALLS WILL PROVIDE QUATITATIVE INFORMATION ON THES COSTS AND ALLOW FDA TO CALCULATE THESE BENEFITS PURSUANT TO E.O. 12291

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Authorizing Statute(s): None

Citations for New Statutory Requirements: None

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Associated Rulemaking Information
RIN:	Stage of Rulemaking:	Federal Register Citation:	Date:

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Federal Register Notices & Comments

Did the Agency receive public comments on this ICR? No

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Number of Information Collection (IC) in this ICR: 1

IC Title	Form No.	Form Name
MEDICAL DEVICE RECALL COST SURVEY

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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	264	0	0	264	0	0
Annual Time Burden (Hours)	178	0	0	178	0	0
Annual Cost Burden (Dollars)	0	0	0	0	0	0

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

Burden Increase Due to:

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

Burden Reduction Due to:

Short Statement:

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Annual Cost to Federal Government: $0

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]? Uncollected

Is this ICR related to the Dodd-Frank Wall Street Reform and Consumer Protection Act, [Pub. L. 111-203]? Uncollected

Is this ICR related to the American Recovery and Reinvestment Act of 2009 (ARRA)? Uncollected

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: 07/19/1993

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