Spud-Queen Lattice Cut recall
Recalled by JR Simplot Company - Headquarters · Boise, ID, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Undeclared wheat.
Undeclared allergen: Wheat
For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.
What was recalled
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 6/4.5 lbs. packages (net wt. 27 lbs.). 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)***".
Quantity: 400 cases
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
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
Where it was sold
Alabama Mississippi
FDA's distribution note: Distributed in AL and MS.
Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. The risk from an undeclared allergen is to people allergic to wheat; for anyone else the product is generally not a safety concern. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- JR Simplot Company - Headquarters
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Dec 18, 2020
- In FDA report of
- Jan 27, 2021
- Terminated
- Jan 20, 2021
- FDA recall number
- F-0208-2021 · event 87015
- Official record
- FDA enforcement report search