RecallRadar
FDA · FoodClass I

Frito-Lay, Inc. Headquarters food recall: Pearl Milling Company Original Pancake & Waffle Mix 32 OZ

Undeclared allergens

Key facts

Agency
U.S. Food and Drug Administration (FDA)
Program
Food
Classification
Class I
Status
Terminated
Event ID
96134
Recall initiated
Jan 14, 2025
Classified by FDA
Feb 13, 2025
Posted in Enforcement Report
Feb 19, 2025
Terminated
Feb 6, 2026
Recalling firm
Frito-Lay, Inc. Headquarters
Firm location
Plano, TX, United States
Initiated by
Voluntary: Firm initiated
Firm notified customers by
Press Release
Products in this event
1

What to do

Compare the product name, size, UPC, lot codes and dates below with the product you have. If it matches, do not eat it. Follow the firm's instructions to return it or throw it away.

View the official FDA record ↗

Reason for recall

Undeclared milk allergen

What the classification means

  • Class I: FDA's most serious category: there is a reasonable probability that using or being exposed to the product will cause serious health problems or death.

About this recall

The firm started this recall on Jan 14, 2025. FDA classified it 30 days later, on Feb 13, 2025. Distribution reported by FDA: Arkansas, Illinois, Indiana, Iowa, Kansas, Kentucky, Minnesota, Mississippi, Nebraska, Utah and Wisconsin. Frito-Lay, Inc. Headquarters has 10 recalls in our records.

Recalled products (1)

  • F-0553-2025 Class I Terminated

    Pearl Milling Company Original Pancake & Waffle Mix 32 OZ (2LB) 907g 30000 65040 BBD SEP 13 25 P

    Codes / lots: BBD SEP 13 25 P

    Quantity: 10,000 cartons

Source and freshness

Source
U.S. Food and Drug Administration (FDA) Enforcement Report, via the openFDA food enforcement dataset
Official notice
FDA Enforcement Report, event 96134
Raw record
openFDA API (JSON)
Dataset last updated by FDA
Nov 3, 2026
Imported by RecallRadar
Nov 4, 2026

Enforcement Report entries describe recalls FDA has classified. They are not always the same as a company press release. If something here differs from FDA's record, FDA's record is correct — please tell us.

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