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# Info Collection Extension Device Recall Authority
- URL: https://www.fdaweb.com/info-collection-extension-device-recall-authority/
- Published: 2018-08-03T12:00:00.000Z
- Updated: 2026-09-15T00:23:39.000Z
- Author: David McFarland
- Tags: FDA Policy/General, #legacy-id-D5142035

*Federal Register* notice: FDA has submitted to OMB an information collection extension for “Medical Device Recall Authority” (OMB Control Number 0910-0432). The information collection implements section 518(e) of the FD&C Act (21 U.S.C. 360h(e)) and part 810 (21 CFR part 810), mandatory medical device recall authority provisions. To view the notice, click [here](https://www.gpo.gov/fdsys/pkg/FR-2018-08-03/pdf/2018-16618.pdf?ref=fdaweb.com).