Food Recall Check
Class I · High risk Terminated Initiated Jan 26, 2022 (5 years ago)

Dunkin Caramel Swirl recall

Recalled by Lyons Magnus, Inc · Fresno, CA, United States

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

Why it was recalled

Undeclared milk allergen due to mislabeling.

Undeclared allergen: Milk

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

Dunkin Caramel Swirl: 6x 64 fl. oz. per case. Product number 4862 UPC case: 10045796048628 Ingredients: Sweetened condensed nonfat milk, high fructose corn syrup, sugar water, brown sugar, caramel color, natural flavors, potassium sorbate (a Preservative), salt. Allergens: Milk Dunkin Mocha Swirl label on inside packages: Ingredients: High Fructose Corn Syrup, Sugar Water, cocoa processed with alkali, natural flavors, citric acid, potassium sorbate (a preservative) salt. Allergens: None Prepared exclusively for Dunkin Brands Canton, MA Case correctly labeled as Caramel Swirl. Individual containers inside case are incorrectly labeled as Dunkin Mocha Swirl - milk is not declared as allergen

Quantity: 1900 cases

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.

Batch 6002 Military time stamp Use by 05/Jul 2022

Where it was sold

Arizona

FDA's distribution note: Initial distribution to AZ

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; 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
Lyons Magnus, Inc
Initiated by
Voluntary: Firm initiated
Recall initiated
Jan 26, 2022
In FDA report of
Mar 2, 2022
Terminated
Apr 29, 2022
FDA recall number
F-0797-2022 · event 89492
Official record
FDA enforcement report search

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