FDA recall record

Super Store Industries-Turlock Dairy Division Sunny Side Farms Peanut Butter Cup Ice Cream recall — FDA F-1772-2018

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.

Class IIclassification
F-1772-2018official record ID
Aug 22, 2018report date

Recall record at a glance

Official recordF-1772-2018
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmSuper Store Industries-Turlock Dairy Division
Report dateAug 22, 2018
Recall initiation dateAug 2, 2018
Quantity8580 cartons ( possible 250 carton affected)
LocationTurlock, CA, United States

Official 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

Why the product 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.

Distribution information

CA, NV

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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