Item #473015 Simplot seasoned CRISP Delivery+ Savory 6 Cut Crinkle Cut Wedge
Reason Undeclared wheat. Product contains wheat but was mis-labeled as Savory 6 Cut Crinkle Cut Wedge and label does not declare wheat.
Simplot¿ Traditional Reduced Sodium Tater Gems¿ recall
Recalled by JR Simplot Company · Boise, ID, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Plastic fragments. Pieces of semi-rigid plastic embedded in the recalled Tater Gems product.
Hard or sharp fragments can cut the mouth or throat, break teeth or cause choking. They usually come from equipment wear or packaging on the production line. All foreign material recalls.
What was recalled
Simplot¿ Traditional Reduced Sodium Tater Gems¿ , formed frozen potatoes, 6/5lb bags per case, foodservice item, master case UPC 100 71179 00418 9. Distributed by Simplot Global Food, LLC, P.O. Box 9386, Boise, ID 83707
Quantity: 7053 cases (6/5lb. bags per case)
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 Code: 087 FEB 16 25 1 Lot Interpretation: 087 - Production Facility FEB - Production Month 16 - Production Date 25 - Production Year 1 Line of Production
Where it was sold
Arkansas Connecticut Georgia Iowa Illinois Indiana Kentucky Louisiana Michigan Minnesota Mississippi North Carolina North Dakota Ohio Oklahoma Tennessee Texas Virginia Wisconsin
FDA's distribution note: Distributed in AR, CT, GA, IA, IL, IN, KY, LA, MI, MN, MS, NC ND, OH, OK, TN, TX, VA and WI.
Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. 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
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Nov 18, 2025
- In FDA report of
- Dec 17, 2025
- Terminated
- Jan 9, 2026
- FDA recall number
- H-0245-2026 · event 98018
- Official record
- FDA enforcement report search