FDA recall record
Label reads in part: TWIN FIN DELI; Gefilte Fish; Kosher Fish Products Inc., Fulton, IL. FDA# 1481764; Net WT. 24 OZ (680G)
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 May 30, 2018. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
Label reads in part: TWIN FIN DELI; Gefilte Fish; Kosher Fish Products Inc., Fulton, IL. FDA# 1481764; Net WT. 24 OZ (680G)
Reason
Lack of adequate HACCP records.
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.
Label reads in part: TWIN FIN DELI; Gefilte Fish; Kosher Fish Products Inc., Fulton, IL. FDA# 1481764; Net WT. 24 OZ (680G)
Code information listed by FDA
Bar Code Number: 4278600076; Lot Number: 12478, 11945, 12694, 12390, 12395r, 12750, 12819, 12367, 12339Revise, 12366, 12670, 12815, 12394.; Manufacture date: 7/2/2013, 7/10/2013, 8/13/2013.
Distribution and firm information
Recalling firm listed by FDA: Schafer Fisheries
Firm location listed by FDA: FULTON, IL, United States
Distribution reported by FDA: US: IL, NY, CA
Product quantity listed by FDA: 250 cases (12 units per case)
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.