FDA recall record
Alfasi Cabernet Kosher Selection Basket #810
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 1, 2017. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
Alfasi Cabernet Kosher Selection Basket #810
Reason
Potential Salmonella contamination.
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.
Alfasi Cabernet Kosher Selection Basket #810
Code information listed by FDA
Lot #LC444152
Distribution and firm information
Recalling firm listed by FDA: Houdini Inc.
Firm location listed by FDA: Fullerton, CA, United States
Distribution reported by FDA: U.S. distribution to the following; nationwide including Puerto Rico.
Product quantity listed by FDA: 31 baskets
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.