FDA recall record
Kraft Singles American Pasteurized Prepared Cheese product, 24 individually wrapped slices in flexible film per pack, net wt. per pack 16oz, keep refrigerated. Single pack is s...
FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.
Product described in an FDA recall
Kraft Singles American Pasteurized Prepared Cheese product, 24 individually wrapped slices in flexible film per pack, net wt. per pack 16oz, keep refrigerated. Single pack is sold at retail. Case UPC 0 00 2100007180 7; Single Pack UPC 0 2100061526 1: Each case contains 27 packs. Case UPC 0 00 2100061450 9; Single Pack UPC 0 2100061526 1: Each case contains 36 packs.
Case UPC 0 00 2100061524 7; Carton UPC 0 2100060491 3; Single Pack UPC 0 2100061526 1; Each case contains 12 cartons, each carton contains 3 packs (72 slices total per carton).
Reason
Plastic fragment. Product is recalled due to potential for a thin strip of the primary packaging film to remain adhered to the cheese slice after the wrapper has been removed.
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.
Kraft Singles American Pasteurized Prepared Cheese product, 24 individually wrapped slices in flexible film per pack, net wt. per pack 16oz, keep refrigerated. Single pack is sold at retail. Case UPC 0 00 2100007180 7; Single Pack UPC 0 2100061526 1: Each case contains 27 packs. Case UPC 0 00 2100061450 9; Single Pack UPC 0 2100061526 1: Each case contains 36 packs.
Case UPC 0 00 2100061524 7; Carton UPC 0 2100060491 3; Single Pack UPC 0 2100061526 1; Each case contains 12 cartons, each carton contains 3 packs (72 slices total per carton).
Code information listed by FDA
Best When Used By Dates on 16oz Single Pack with the UPC of 0 2100061526 1 are: 10 JAN 24 S 72 through 27 JAN 24 S 72 Best When Used By Dates on 16oz Single Pack from the 3lb multipack carton with the UPC of 0 2100060491 3 are: 09 JAN 2024 through 13 JAN 2024, and 16 JAN 2024. Manufacturer Code on Case (UPC 0 00 2100061450 9): DD JAN 24 S 72/73 TT:TT. DD would be between 10-27.
Manufacturer Code on Case (UPC 0 00 2100007180 7): XB ZZZ 23 021 DD JAN 2024. ZZZ would be between 163-165, 167, 169-173. Manufacturer Code on Case (UPC 0 00 2100061524 7): XB DDD 23 021 DD JAN 2024. DDD would be between 164-168, 171. DD would be between 09-13, and 16.
Distribution and firm information
Recalling firm listed by FDA: HEINZ
Firm location listed by FDA: Chicago, IL, United States
Distribution reported by FDA: Distributed nationwide and in Puerto Rico.
Product quantity listed by FDA: Total 83,802 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.