Dierbergs Kitchen 16 oz Mac & Cheese packaged in a black plastic container with a clear plastic lid with a white label,
Summary
The FDA issued a Class II for Dierbergs Kitchen 16 oz Mac & Cheese packaged in a black plastic container with by Dierbergs Markets, Inc.. Reason: Undeclared allergens (wheat) on label, incorrect label was placed on product.
Details
Source
Food Recall
External ID
F-0469-2025
Action Date
2025-02-12
Status
Terminated
Category
food
Product Description
Dierbergs Kitchen 16 oz Mac & Cheese packaged in a black plastic container with a clear plastic lid with a white label, The label states "Dierbergs Kitchen Homestyle Mashed Potatoes UPC 231220-006538"
Lot/Code Info: Use by date 1/9/2025
Quantity Affected: 298 packages
Reason for Recall
Undeclared allergens (wheat) on label, incorrect label was placed on product
Distribution
Retail locations in MO and IL
Type: Voluntary: Firm initiated
Recall Initiated: 2025-01-03
Company
Bridgeton, MO
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 106 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
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 (Dierbergs Markets, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Dierbergs Markets, Inc. have FDA actions?
This is the only FDA action we have on record for Dierbergs Markets, Inc. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0469-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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