Food Recall Check
Class I · High risk Terminated Initiated Feb 14, 2014 (13 years ago)

Chocolate Ice Cream manufactured under the Dairy Rich brand and packaged in a 1.75 quart recall

Recalled by Ice Cream Specialities · Carlinville, IL, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

This voluntary recall has been initiated because Dairy Rich Chocolate Ice Cream may contain peanut butter, which contains a peanut allergen.

Undeclared allergens: Milk Peanut

For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.

What was recalled

Chocolate Ice Cream manufactured under the Dairy Rich brand and packaged in a 1.75 quart (1.66 L) (56 oz.) carton.

Quantity: 2,448 cartons

Food: Ice cream Chocolate & candy

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.

Best By: 06/14/2015. UPC: 0-71580-08103-1.

Where it was sold

Illinois Indiana New York

FDA's distribution note: US: IL, IN, NY

Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. The risk from an undeclared allergen is to people allergic to milk, peanut; for anyone else the product is generally not a safety concern. 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
Ice Cream Specialities
Initiated by
Voluntary: Firm initiated
Recall initiated
Feb 14, 2014
In FDA report of
Mar 12, 2014
Terminated
Mar 30, 2017
FDA recall number
F-1610-2014 · event 67530
Official record
FDA enforcement report search

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