FDA recall record
TETAS Mireya, SABOR Toddy
FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.
FDA listed a termination date of September 29, 2023. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
TETAS Mireya, SABOR Toddy
Reason
Undeclared allergens: Soy
Products involved
Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.
TETAS Mireya, SABOR Toddy
Code information listed by FDA
Exp. Date 10/31/23
Distribution and firm information
Recalling firm listed by FDA: DIBE LLC
Firm location listed by FDA: Miami, FL, United States
Distribution reported by FDA: Domestic distribution only.
Product quantity listed by FDA: 250 units/6 oz ea.
Source
Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.
Official FDA openFDA food enforcement record
Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.