Dunkin Caramel Swirl: 6x 64 fl. oz. per case. Product number 4862 UPC case: 10045796048628 Ingredients: Sweetened
Summary
The FDA issued a Class I for Dunkin Caramel Swirl: 6x 64 fl. oz. per case. Product number 4862 UPC case: by Lyons Magnus, Inc. Reason: Undeclared milk allergen due to mislabeling..
Details
Source
Food Recall
External ID
F-0797-2022
Action Date
2022-03-02
Status
Terminated
Category
food
Product Description
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
Lot/Code Info: Batch 6002 Military time stamp Use by 05/Jul 2022
Quantity Affected: 1900 cases
Reason for Recall
Undeclared milk allergen due to mislabeling.
Distribution
Initial distribution to AZ
Type: Voluntary: Firm initiated
Recall Initiated: 2022-01-26
Company
Fresno, CA
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 65 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Lyons Magnus, Inc has 78 FDA actions in our database, including 78 recalls.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Lyons Magnus, Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Lyons Magnus, Inc have FDA actions?
Lyons Magnus, Inc has 78 FDA actions in our database, including 78 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0797-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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