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# Info Collection on Device Recall Authority
- URL: https://www.fdaweb.com/info-collection-on-device-recall-authority/
- Published: 2024-06-04T12:00:00.000Z
- Updated: 2026-09-14T14:32:25.000Z
- Author: David McFarland
- Tags: FDA Policy/General, #legacy-id-D5157105

*Federal Register* notice: FDA is seeking comments on an information collection extension entitled “Medical Device Recall Authority — 21 CFR Part 810.” The collection supports agency regulations that set forth mandatory medical device recall authority provisions. For example, it covers FDA’s authority to issue a recall order if it finds that there is reasonable probability that a device intended for human use would cause serious, adverse health consequences or death. To view the notice, click [here](https://public-inspection.federalregister.gov/2024-12346.pdf?ref=fdaweb.com).