Food recall

Lyons Magnus, Inc recall: Dunkin Caramel Swirl

Lyons Magnus, Inc, of Fresno, CA, recalled Dunkin Caramel Swirl. The FDA's reason: “Undeclared milk allergen due to mislabeling.” The FDA classified it Class I: it could cause serious harm or death. The company began the recall voluntarily on January 26, 2022, and the FDA first listed it in its Enforcement Report of March 2, 2022. The FDA has closed the recall: it found the company did all it reasonably could to remove or correct the product.

How serious

Class I

It could cause serious harm or death

Why

Allergen not on the label

Status

Terminated

Closed April 29, 2022

The recall

Company
Lyons Magnus, Inc (Fresno, CA)
Reason, in FDA's words
“Undeclared milk allergen due to mislabeling.”
Where it was sold
Initial distribution to AZ
Recall began
, by the company
FDA classified it
First in an FDA Enforcement Report
FDA event number
89492

The product recalled

As the FDA describes them, with the codes that tell whether a package is part of the recall.

  • F-0797-2022 Class I

    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

    Codes: Batch 6002 Military time stamp Use by 05/Jul 2022

    Quantity: 1900 cases

Get new charts weekly

One email a week with the newest charts and their key numbers. No account needed.

Source and notes

U.S. Food and Drug Administration, Enforcement Reports (openFDA food recall data) (Public domain (U.S. government work); source U.S. Food and Drug Administration, openFDA), data as of March 2, 2022.

Each week the FDA lists the recalls it has classified in its Enforcement Report, often weeks after the company announced the recall, so a month with five weekly reports tends to count more. Each recall counts once, however many products it covers, in the month FDA first listed it. Class I means the food could cause serious harm or death, Class II temporary or minor harm, and Class III is unlikely to harm anyone. Meat, poultry and most egg products are recalled by the U.S. Department of Agriculture, not the FDA, and aren't included. For what to do with a recalled product, see the FDA's recalls page.