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# Info Collection on Device Risk Allegations
- URL: https://www.fdaweb.com/info-collection-on-device-risk-allegations/
- Published: 2020-02-10T12:00:00.000Z
- Updated: 2026-09-14T16:02:27.000Z
- Author: David McFarland
- Tags: FDA Policy/General, #legacy-id-D5146054

*Federal Register* notice: FDA is seeking comments on an information collection entitled “Electronic Submission Process for Voluntary Allegations to the Center for Devices and Radiological Health” (OMB Control Number 0910-0769). The collection involves information voluntarily submitted to CDRH on actual or potential health risk concerns about a medical device or radiological product or its use. CDRH has established a format and process for such submissions. To view the notice, click [here](https://www.govinfo.gov/content/pkg/FR-2020-02-10/pdf/2020-02530.pdf?ref=fdaweb.com).