Class ITerminatedVoluntary: Firm initiated
Frito-Lay, Inc. Headquarters: food recall F-0553-2025
Frito-Lay, Inc. Headquarters of Plano, TX recalled Pearl Milling Company Original Pancake & Waffle Mix 32 OZ (2LB) 907g 30000 65040 BBD SEP 13 25 P. Reason: Undeclared milk allergen. The FDA listed it as Class I in its Enforcement Report dated Feb 19, 2025; distribution: Arkansas, Iowa, Illinois, Indiana, Kansas, Kentucky, Minnesota, Mississippi, Nebraska, Utah, Wisconsin.
Record status as published: Terminated (terminated Feb 6, 2026). 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
- Pearl Milling Company Original Pancake & Waffle Mix 32 OZ (2LB) 907g 30000 65040 BBD SEP 13 25 P
- Product quantity
- 10,000 cartons
- Reason for recall
- Undeclared milk allergen
- Codes, lots and dates on the package
- BBD SEP 13 25 P
- Distribution pattern
- Arkansas, Illinois, Indiana, Iowa, Kansas, Kentucky, Minnesota, Mississippi, Nebraska, Utah and Wisconsin.
- Recalling firm
- Frito-Lay, Inc. Headquarters, Plano, TX
- Classification
- Class I — the FDA uses this class for a situation in which there is a reasonable probability that using or being exposed to the product will cause serious adverse health consequences or death.
- 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 14, 2025 |
| Classified by the FDA | Feb 13, 2025 |
| Published in the Enforcement Report | Feb 19, 2025 |
| Terminated | Feb 6, 2026 |
Other recalls by Frito-Lay, Inc. Headquarters
- F-0688-2025 · Apr 9, 2025 · Class I — Undeclared allergen (milk).
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number F-0553-2025 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
- Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service. The FDA does not endorse OpenPlate.