Class IITerminatedVoluntary: Firm initiated
Dierbergs Markets, Inc.: food recall F-0469-2025
Dierbergs Markets, Inc. of Bridgeton, MO recalled Dierbergs Kitchen 16 oz Mac & Cheese packaged in a black plastic container with a clear plastic lid with a white… Reason: Undeclared allergens (wheat) on label, incorrect label was placed on product. The FDA listed it as Class II in its Enforcement Report dated Feb 12, 2025; distribution: Illinois, Missouri.
Record status as published: Terminated (terminated Feb 5, 2025). openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- Product
- 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"
- Product quantity
- 298 packages
- Reason for recall
- Undeclared allergens (wheat) on label, incorrect label was placed on product
- Codes, lots and dates on the package
- Use by date 1/9/2025
- Distribution pattern
- Retail locations in MO and IL
- Recalling firm
- Dierbergs Markets, Inc., Bridgeton, MO
- Classification
- Class II — the FDA uses this class for a situation in which using or being exposed to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
- Press Release
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Jan 3, 2025 |
| Classified by the FDA | Feb 4, 2025 |
| Published in the Enforcement Report | Feb 12, 2025 |
| Terminated | Feb 5, 2025 |
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number F-0469-2025 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
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