CFR›Title 21›Chapter I›Part 810 ContainsSubparts A–BCorpusDaily eCFRDisplayed edition2026-05-13Last updated2026-05-13 PART 810—MEDICAL DEVICE RECALL AUTHORITY Subparts A Subpart A—General Provisions Sections 810.1–810.4 B Subpart B—Mandatory Medical Device Recall Procedures Sections 810.10–810.18 Authority21 U.S.C. 321, 331, 332, 333, 334, 351, 352, 355, 360h, 360i, 371, 374, 375.Source61 FR 59018, Nov. 20, 1996, unless otherwise noted. Previous 809 Part 809—In Vitro Diagnostic Products for Human Use Next 812 Part 812—Investigational Device Exemptions