Sunnyside Farms Prestirred Peach Yogurt With Other Natural Flavors
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Sunny Side Farms Peanut Butter Cup Ice Cream recall
Recalled by Super Store Industries-Turlock Dairy Division · Turlock, CA, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Some containers of ice cream in a Peanut Butter Cup flavor container have a Butter Pecan flavor lid and are filled with Butter Pecan ice cream.
These are failures of the safety steps that keep food safe - cooking, pasteurising, keeping cold, sealing - even when no contaminant has yet been found. All processing & sanitation problems recalls.
What was recalled
Sunny Side Farms Peanut Butter Cup Ice Cream; 48 oz. carton, 1.5 QTS (1.42L) UPC: 7-17544-20740 5 Allergens for Peanut Butter Cup: Milk, Peanuts, Soy, Coconut. Allergens for Butter Pecan: Milk, Pecans Both packages include the following statement: While best practices and preventive measures are taken to control allergen cross contamination, this product is produced in a facility that also manufactures items with peanuts, tree nuts, wheat, soy and egg. Distributed by Super Store Industries, PO Box 549, Lathrop, CA
Quantity: 8580 cartons ( possible 250 carton affected)
Food: Ice cream Peanut butter
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 & BEST BY DATE: 07/14/2019
Where it was sold
California Nevada
FDA's distribution note: CA, NV
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
- Super Store Industries-Turlock Dairy Division
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Aug 2, 2018
- In FDA report of
- Aug 22, 2018
- Terminated
- Aug 10, 2018
- FDA recall number
- F-1772-2018 · event 80705
- Official record
- FDA enforcement report search
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