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# Info Collection on FDA Recall Regulations
- URL: https://www.fdaweb.com/info-collection-on-fda-recall-regulations-2/
- Published: 2021-04-08T12:00:00.000Z
- Updated: 2026-09-14T16:54:14.000Z
- Author: David McFarland
- Tags: FDA Policy/General, #legacy-id-D5149066

*Federal Register* notice: FDA has submitted to OMB an information collection extension entitled “FDA Recall Regulations — 21 CFR Part 7” (OMB Control Number 0910-0249). The collection pertains to product recalls, which may be undertaken voluntarily and at any time by manufacturers and distributors, or at the request of the agency. Recalls are terminated when all reasonable efforts have been made to remove or correct the product in accordance with the recall strategy. The regulations also call for corrective actions to be taken regarding violative products and establish specific requirements that enable the agency to monitor and assess the adequacy of a firm’s actions. To view the notice, click [here](https://public-inspection.federalregister.gov/2021-07287.pdf?ref=fdaweb.com).