CLASS I Food recall · Reported 19 Feb 2025 · FDA Enforcement Report
Pearl Milling Company Original Pancake & Waffle Mix recalled
Frito-Lay, Inc. Headquarters is recalling Pearl Milling Company Original Pancake & Waffle Mix 30000 65040 BBD SEP 13 25 P, distributed in 11 states. The recall was initiated on 14 Jan 2025 and the FDA has classified it as Class I.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- F-0553-2025
- FDA event ID
- 96134
- Recalling firm
- Frito-Lay, Inc. Headquarters, Plano, TX
- Brand
- Pearl Milling
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 14 Jan 2025
- FDA classified
- 13 Feb 2025
- Reported
- 19 Feb 2025
- Type
- Voluntary: Firm initiated
- Customers notified by
- Press Release
- Reason category
- Undeclared Milk
- Product category
- Other
Timeline
| 14 Jan 2025 | Recall initiated by company | |
| 13 Feb 2025 | Classified by FDA | +30 days |
| 19 Feb 2025 | Published in enforcement report | +6 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Undeclared milk allergen
Product as listed by the FDA
Pearl Milling Company Original Pancake & Waffle Mix 32 OZ (2LB) 907g 30000 65040 BBD SEP 13 25 P
Where it was distributed
Arkansas, Illinois, Indiana, Iowa, Kansas, Kentucky, Minnesota, Mississippi, Nebraska, Utah and Wisconsin.
ArkansasIowaIllinoisIndianaKansasKentuckyMinnesotaMississippiNebraskaUtahWisconsin
Questions about this recall
Why was it recalled?
Undeclared milk allergen
Which lots are affected?
BBD SEP 13 25 P
Where was it sold?
Arkansas, Illinois, Indiana, Iowa, Kansas, Kentucky, Minnesota, Mississippi, Nebraska, Utah and Wisconsin.
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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