{"data":{"id":"us/21-cfr-107.220","jurisdiction":"us","citation":"21 CFR 107.220","heading":"Scope and effect of infant formula recalls.","body":"(a) The requirements of this subpart apply:\n(1) When the Food and Drug Administration has determined that it is necessary to remove from the market a distributed infant formula that is in violation of the laws and regulations administered by the Food and Drug Administration and that poses a risk to human health; or\n(2) When a manufacturer has determined that it is necessary to remove from the market a distributed infant formula that:\n(i) Is no longer subject to the manufacturer's control;\n(ii) Is in violation of the laws and regulations administered by the Food and Drug Administration and against which the agency could initiate legal or regulatory action; and\n(iii) Does not present a human risk.\n(b) The Food and Drug Administration will monitor continually the recall action and will take appropriate actions to ensure that the violative infant formula is removed from the market.","path":["Title 21—Food and Drugs","CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES","SUBCHAPTER B—FOOD FOR HUMAN CONSUMPTION","PART 107—INFANT FORMULA","Subpart E—Infant Formula Recalls"],"source_url":"https://www.ecfr.gov/api/versioner/v1/full/2026-08-25/title-21.xml","current_through":"2026-08-25","vintage":"","retrieved_at":"2026-08-27T02:24:47Z","sha256":"10b8205d55aea9e1616d04c6fbf08892f7b890f1e68b3a0743910bdb5895ae0a","source_id":"us-cfr","stale":true,"prev":"us/21-cfr-107.210","next":"us/21-cfr-107.230"},"notice":"GroundRules: Original legal text. Not legal advice."}