Class IITerminated in FDA datasetAug 2, 2018

Sunny Side Farms Peanut Butter Cup Ice Cream; 48 oz. carton, 1.5 QTS (1.42L)

Recalling firm: Super Store Industries-Turlock Dairy Division

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.

Check your package

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

ProductSunny 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
UPC717544207405

FDA code information

LOT & BEST BY DATE: 07/14/2019

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

Full FDA record and distribution details

Original product description

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

Extracted codes and context

TypeCode / valueContext
UPC717544207405y 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 pa

Recall details

Recall number
F-1772-2018
Event ID
80705
FDA status
Terminated
Initiated
Aug 2, 2018
Reported
Aug 22, 2018
Classified
Aug 10, 2018
Terminated
Aug 10, 2018
Quantity
8580 cartons ( possible 250 carton affected)
Location
Turlock, CA, United States
Initiation type
Voluntary: Firm initiated
Notification
E-Mail

Where it was distributed

CA, NV

FDA source record · F-1772-2018

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

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