CFR›Title 21›Chapter I›Part 810 ContainsSubparts A–BCorpusDaily eCFRDisplayed edition2026-09-30Last updated2026-09-30 PART 810—MEDICAL DEVICE RECALL AUTHORITY Subparts A Subpart A—General Provisions B Subpart B—Mandatory Medical Device Recall Procedures 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.