Pearl Milling Company Original Pancake & Waffle Mix 32 OZ (2LB) 907g 30000 65040 BBD SEP 13 25 P
Summary
The FDA issued a Class I for Pearl Milling Company Original Pancake & Waffle Mix 32 OZ (2LB) 907g 30000 650 by Frito-Lay, Inc. Headquarters. Reason: Undeclared milk allergen.
Details
Source
Food Recall
External ID
F-0553-2025
Action Date
2025-02-19
Status
Terminated
Category
food
Product Description
Pearl Milling Company Original Pancake & Waffle Mix 32 OZ (2LB) 907g 30000 65040 BBD SEP 13 25 P
Lot/Code Info: BBD SEP 13 25 P
Quantity Affected: 10,000 cartons
Reason for Recall
Undeclared milk allergen
Distribution
Arkansas, Illinois, Indiana, Iowa, Kansas, Kentucky, Minnesota, Mississippi, Nebraska, Utah and Wisconsin.
Type: Voluntary: Firm initiated
Recall Initiated: 2025-01-14
Company
Plano, TX
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 106 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Frito-Lay, Inc. Headquarters has 8 FDA actions in our database, including 8 recalls.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Frito-Lay, Inc. Headquarters) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Frito-Lay, Inc. Headquarters have FDA actions?
Frito-Lay, Inc. Headquarters has 8 FDA actions in our database, including 8 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0553-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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