FDA recall record
205190-50 Cumin Seed Powder
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 June 24, 2015. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
205190-50 Cumin Seed Powder
Reason
Notified by immediate supplier of recall of ground cumin from Turkey due to the presence of 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.
205190-50 Cumin Seed Powder
Code information listed by FDA
Lot 81533-51
Distribution and firm information
Recalling firm listed by FDA: Starwest Botanicals, Inc
Firm location listed by FDA: Sacramento, CA, United States
Distribution reported by FDA: One customer in MO
Product quantity listed by FDA: 300 lbs.
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.