Class ITerminated in FDA datasetRecall initiated Mar 4, 2014

Belmont Premium Ice Cream, Chocolate Chip Cookie Dough, All Natural, 1.5 Quarts (1.42 L),…

Recalling firm: House Of Flavors, Inc.

Why it was recalled

may contain undeclared nut allergen.

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: May 12, 2014.

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ProductBelmont Premium Ice Cream, Chocolate Chip Cookie Dough, All Natural, 1.5 Quarts (1.42 L), Nutrition Facts....., Ingredients: Skim milk, Cream, Sugar, Cookie dough pieces (unenriched wheat flour, sugar, butter (cream, salt), brown sugar, water, corn oil, fructose, corn syrup solids, salt, vanilla extract, sodium bicarbonate, coconut oil) corn syrup, chocolate flakes (sugar, coconut oil, cocoa processed with alkali, butter oil, soy lecithin, natural flavor, whey flavor base ( brown sugar, water, natural flavor, molasses, salt) egg, carob bean gum, guar gum, carrageenan, annatto (color), Contains: milk, wheat , egg, soy Distributed by ALDI Inc. Batavia, IL 60510, UPC code 4149816310

FDA code information

date code 13340 and 13341, Best by Date: Dec. 7, 2014

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Full FDA record and distribution details

Original product description

Belmont Premium Ice Cream, Chocolate Chip Cookie Dough, All Natural, 1.5 Quarts (1.42 L), Nutrition Facts....., Ingredients: Skim milk, Cream, Sugar, Cookie dough pieces (unenriched wheat flour, sugar, butter (cream, salt), brown sugar, water, corn oil, fructose, corn syrup solids, salt, vanilla extract, sodium bicarbonate, coconut oil) corn syrup, chocolate flakes (sugar, coconut oil, cocoa processed with alkali, butter oil, soy lecithin, natural flavor, whey flavor base ( brown sugar, water, natural flavor, molasses, salt) egg, carob bean gum, guar gum, carrageenan, annatto (color), Contains: milk, wheat , egg, soy Distributed by ALDI Inc. Batavia, IL 60510, UPC code 4149816310

Original FDA recall reason

may contain undeclared nut allergen.

Recall details

Recall number
F-1726-2014
Event ID
67667
FDA status
Terminated
Initiated
Mar 4, 2014
Reported
Apr 9, 2014
Classified
Mar 31, 2014
Terminated
May 12, 2014
Quantity
26,534 units
Location
Ludington, MI, 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

IN, IL, MI, OH

FDA source record · F-1726-2014

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

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