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Snapshot · OMB 2025 inventory · processed Oct 11, 2026
HHS · no agency ID · record R0851

FOIA REDACTION (FRED) TOOL

Department of Health and Human Services · HHS/FDA/CDER

Overview

Development stage
DeployedSource: c) Deployed – The use case is being actively authorized or utilized to support the functions or mission of an agency.
High-impact designation
Presumed high-impact, determined notSource: b) Presumed high-impact, but determined not high impact
Impact justification
FRED should not be considered a high-impact AI use case because: a. It operates as a recommendation system only, with mandatory human review and approval required for all outputs. b. No automated decisions are made - humans retain full control over all redaction decisions. c. It serves as an assistive tool to improve efficiency while maintaining human oversight and accountability for all FOIA compliance decisions.
Start date
2025-05 (month precision)Source: May-25
Withheld from public reporting
NoSource: a) No

Mission

Topic area
Health and Medical
Operational functions
FOIA and records management Derived by keyword rules; see methodology

Problem the AI is intended to solve

FRED is designed to support FOIA staff in redacting records more efficiently and consistently. FOIA redaction can be a time-consuming process and experience large back-logs of requested documents. It aims to use AI to analyze, identify, and generate predictions of text for redaction, thereby improving the efficiency of FOIA response processing.

Expected benefits

More efficient releases of documents in response to FOIA requests, reduction in back-logs, helping ensure public access to government information while protecting sensitive data appropriately.

System outputs

FRED produces a PDF with boxes around text that it recommends for redaction along with comments for the redaction code

Technology

AI classification
Generative AISource: Generative AI: AI that generates new or synthetic content (e.g., images, videos, audio, text, code).
System name(s)
Elsa
Custom-developed code
Yes
Public source code
Not reported

Sourcing

How it was built
Contract and in-houseSource: c) Developed with both contracting and in-house resources
Vendor (as reported)
Contractor teams
Vendors (standardized)
None on the standard list

A vendor is the supplier named by the agency. It does not identify the underlying model or AI technology.

Data and privacy

Involves PII
Yes
Privacy Impact Assessment
Not reported
Authorization to Operate
Yes
Demographic features
k) None of the above
Training and evaluation data
Completed 483 forms before redaction and versions of those forms after redaction by FDA staff
Federal Data Catalog
Not reported

Governance

0 of 8 minimum-practice questions answered. A blank answer means the agency reported nothing; it does not mean the practice is absent.

Pre-deployment testingNo answer reported
AI impact assessmentNo answer reported
Independent reviewNo answer reported
Ongoing monitoringNo answer reported
Operator trainingNo answer reported
Fail-safeNo answer reported
Appeal processNo answer reported
User and public consultationNo answer reported

Potential impacts and how they were identified

Not reported