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# Info Collection on Device Corrections and Removals
- URL: https://www.fdaweb.com/info-collection-on-device-corrections-and-removals/
- Published: 2020-08-20T12:00:00.000Z
- Updated: 2026-09-14T16:25:48.000Z
- Author: David McFarland
- Tags: FDA Policy/General, #legacy-id-D5147474

*Federal Register* notice: FDA has submitted to OMB an information collection entitled “Medical Devices; Reports of Corrections and Removals — 21 CFR part 806” (OMB Control Number 0910–0359). The collection supports FDA regulations that require, within 10 working days of initiating any action to correct or remove a device to reduce a risk to health posed by the device or to remedy a violation of the FD&C Act, device manufacturers or importers to submit a written report about the correction or removal. To view the notice, click [here](https://www.govinfo.gov/content/pkg/FR-2020-08-20/pdf/2020-18269.pdf?ref=fdaweb.com).