US lawFederal (United States)RegulationsTitle 21 CFR — Food and DrugsChapter I — FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICESPart 810 — MEDICAL DEVICE RECALL AUTHORITYSubpart A — General Provisions810.121 C.F.R. § 810.1Scope.Last amended: 2016Year: 2026Length: 31 wordsOfficial source Cite as 21 C.F.R. § 810.1 (2026)Part 810 describes the procedures that the Food and Drug Administration will follow in exercising its medical device recall authority under section 518(e) of the Federal Food, Drug, and Cosmetic Act.Next21 C.F.R. § 810.2