Class ITerminated in FDA datasetRecall initiated Dec 18, 2020

SPUD-QUEEN LATTICE CUT - SKIN ON FROZEN POTATOES, master case SKU 10071179 041290.

Recalling firm: JR Simplot Company - Headquarters

Why it was recalled

Undeclared wheat.

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Jan 20, 2021.

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Compare the exact product and package details with the label you have.

ProductSPUD-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)***".
Package size4.5 lbs

FDA code information

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

Match the product, package size, and code together. A missing match does not guarantee safety.

Full FDA record and distribution details

Original product description

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)***".

Original FDA recall reason

Undeclared wheat.

Recall details

Recall number
F-0208-2021
Event ID
87015
FDA status
Terminated
Initiated
Dec 18, 2020
Reported
Jan 27, 2021
Classified
Jan 15, 2021
Terminated
Jan 20, 2021
Quantity
400 cases
Location
Boise, ID, United States
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

Distributed in AL and MS.

FDA source record · F-0208-2021

Data updated September 16, 2026. View official FDA data ↗

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