FDA recall record
Sazon Coriander & Annatto
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 January 24, 2017. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
Sazon Coriander & Annatto
Reason
Cumin used was contaminated with peanut protein.
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.
Sazon Coriander & Annatto
Code information listed by FDA
41 oz - UPC: 4133103782, Lots: 101065, 301065, 101075, 301075, 101085, and 101095.
Distribution and firm information
Recalling firm listed by FDA: Sazon, Inc.
Firm location listed by FDA: Doral, FL, United States
Distribution reported by FDA: US- NY, TX, FL, PA, PR, IL, VA, MA
Product quantity listed by FDA: 40,569
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.