{"data":{"id":"us/21-cfr-107.200","jurisdiction":"us","citation":"21 CFR 107.200","heading":"Food and Drug Administration-required recall.","body":"When the Food and Drug Administration determines that an adulterated or misbranded infant formula presents a risk to human health, a manufacturer shall immediately take all actions necessary to recall that formula, extending to and including the retail level, consistent with the requirements of this subpart.","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":"d51992c2d607ce48901a9f604d84abb64d97cfe4b3cf1093aa963699206e81d6","source_id":"us-cfr","stale":true,"prev":"us/21-cfr-107.100","next":"us/21-cfr-107.210"},"notice":"GroundRules: Original legal text. Not legal advice."}