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Frito-Lay, Inc. Headquarters Recall: Undeclared milk allergen

United States

TerminatedClass I

Company
Frito-Lay, Inc. Headquarters
Product
Pearl Milling Company Original Pancake & Waffle Mix 32 OZ (…
Recall date
January 14, 2025
Terminated
February 6, 2026
Source
FDA

Reason for recall

Undeclared milk allergen

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Pearl Milling Company Original Pancake & Waffle Mix 32 OZ (2LB) 907g 30000 65040 BBD SEP 13 25 P Not published in this source record 10,000 cartons BBD SEP 13 25 P

Distribution

  • Arkansas
  • Illinois
  • Indiana
  • Iowa
  • Kansas
  • Kentucky
  • Minnesota
  • Mississippi
  • Nebraska
  • Utah and Wisconsin.

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0553-2025
Event ID
96134
Status
Terminated
Classification
Class I
Company
Frito-Lay, Inc. Headquarters
Product description
Pearl Milling Company Original Pancake & Waffle Mix 32 OZ (2LB) 907g 30000 65040 BBD SEP 13 25 P
Quantity
10,000 cartons
Reason
Undeclared milk allergen
Recall initiation date
January 14, 2025
Report date
February 19, 2025
Classification date
Not published in this source record
Termination date
February 6, 2026
Distribution pattern
Arkansas, Illinois, Indiana, Iowa, Kansas, Kentucky, Minnesota, Mississippi, Nebraska, Utah and Wisconsin.
UPC, lot, and code information
BBD SEP 13 25 P
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Press Release
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: Frito-Lay, Inc. Headquarters

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Distribution
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Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class I mean?

A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.