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# Info Collection for Device Corrections/Removals
- URL: https://www.fdaweb.com/info-collection-for-device-corrections-removals/
- Published: 2020-02-21T12:00:00.000Z
- Updated: 2026-09-14T16:04:05.000Z
- Author: David McFarland
- Tags: FDA Policy/General, #legacy-id-D5146141

*Federal Register* notice: FDA is seeking comments on an information collection extension for “Medical Devices; Reports of Corrections and Removals — 21 CFR Part 806” (OMB Control Number 0910-0359). The agency’s regulations require that within 10 working days of initiating any action to correct or remove a device to reduce a risk to health or to remedy a violation caused by the device that may present a risk to health, device manufacturers or importers must submit a written report about the issue. To view the notice, click [here](https://www.govinfo.gov/content/pkg/FR-2020-02-21/pdf/2020-03458.pdf?ref=fdaweb.com).