FDA recall record
SPUD-QUEEN LATTICE CUT - SKIN ON FROZEN POTATOES, master case SKU 10071179 041290. Distributed by Mid America Potato Company P.O. BOX 9386 BOISE, ID. Each case contains 6/4....
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 January 20, 2021. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
SPUD-QUEEN LATTICE CUT - SKIN ON FROZEN POTATOES, master case SKU 10071179 041290. O. BOX 9386 BOISE, ID. 5 lbs. packages (net wt. ). Product is a foodservice item and product is packaged in a clear bag and has no label.
The Master Case label is read in parts: "*** SPUD-QUEEN LATTICE CUT - SKIN ON FROZEN POTATOES ***INGREDIENTS: POTATOES, VEGETABLE OIL (SOYBEAN, CANOLA, COTTONSEED, AND/OR SUNFLOWER), CONTAINS LESS THAN 2% OF DEXTROSE, DISODIUM DIHYDROGEN PYROPHOSPHATE (TO MAINTAIN NATURAL COLOR)***".
Reason
Undeclared wheat.
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.
SPUD-QUEEN LATTICE CUT - SKIN ON FROZEN POTATOES, master case SKU 10071179 041290. O. BOX 9386 BOISE, ID. 5 lbs. packages (net wt. ). Product is a foodservice item and product is packaged in a clear bag and has no label.
The Master Case label is read in parts: "*** SPUD-QUEEN LATTICE CUT - SKIN ON FROZEN POTATOES ***INGREDIENTS: POTATOES, VEGETABLE OIL (SOYBEAN, CANOLA, COTTONSEED, AND/OR SUNFLOWER), CONTAINS LESS THAN 2% OF DEXTROSE, DISODIUM DIHYDROGEN PYROPHOSPHATE (TO MAINTAIN NATURAL COLOR)***".
Code information listed by FDA
Lot Codes printed on clear packages and on the side of the master case: 200APR062001 and 200APR072001 200 = Production Facility APR = Production Month (April) 06 or 07 = Production Day 20 = Production Year 01 = Line
Distribution and firm information
Recalling firm listed by FDA: JR Simplot Company - Headquarters
Firm location listed by FDA: Boise, ID, United States
Distribution reported by FDA: Distributed in AL and MS.
Product quantity listed by FDA: 400 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.