FDA recall record
BADIA Ground Cumin
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 March 30, 2017. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
BADIA Ground Cumin
Reason
Undeclared 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.
BADIA Ground Cumin
Code information listed by FDA
2 oz. - Lot 117151, UPC 033844-00002-8; 7 oz. - Lot 116837, UPC 033844-00007-3; 16 oz. - Lot 116696, UPC 033844-00516-0.
Distribution and firm information
Recalling firm listed by FDA: Badia Spices, Inc.
Firm location listed by FDA: Miami, FL, United States
Distribution reported by FDA: FL, TX, ID, WA, MA, MD, NY, MN, PA, NH, KS, AR, NC, CA, CT, GA, CO, MI, NJ. and St. Thomas, USVI Foreign: Canada, Netherlands, Cayman Islands, St. Kitts, Grenada, Honduras, Costa Rica, Dominica, Colombia, Curacao, Bonaire, Tortola and St. Maarten.
Product quantity listed by FDA: 13,216 cases
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.