Food recall

C.H. Guenther & Son, Inc. recall: 235214 Baker's Source Traditional Cornbread Mix Complete

C.H. Guenther & Son, Inc., of San Antonio, TX, recalled 235214 Baker's Source Traditional Cornbread Mix Complete. The FDA's reason: “Undeclared egg allergen.” The FDA classified it Class I: it could cause serious harm or death. The company began the recall voluntarily on December 10, 2024, and the FDA first listed it in its Enforcement Report of January 15, 2025. The FDA has closed the recall: it found the company did all it reasonably could to remove or correct the product.

How serious

Class I

It could cause serious harm or death

Why

Allergen not on the label

Status

Terminated

Closed February 21, 2025

The recall

Company
C.H. Guenther & Son, Inc. (San Antonio, TX)
Reason, in FDA's words
“Undeclared egg allergen”
Where it was sold
Louisiana, Tennessee, Texas, Oklahoma, Arkansas, Missouri, Florida, Virginia
Recall began
, by the company
FDA classified it
First in an FDA Enforcement Report
FDA event number
95965

The product recalled

As the FDA describes them, with the codes that tell whether a package is part of the recall.

  • F-0384-2025 Class I

    235214 Baker's Source Traditional Cornbread Mix Complete, 5 LB Bags, 30 LB Cases Foodservice Use, Human Consumption & mix with water and bake Shelf Stable Dry Mix, 1 Year Shelf Life

    Codes: Item: 235214 6/5# Baker s Source Traditional Cornbread Mix MFG Dates Lot Codes 5/22/2024 PF052224 6/24/2024 PF062424 6/25/2024 PF062524 7/25/2024 PF072524 7/26/2024 PF072624 8/21/2024 PF082124 8/22/2024 PF082224 9/16/2024 PF091626 9/18/2024 PF091824 9/20/2024 PF092024 10/4/2024 PF100424 10/5/2024 PF100524 10/23/2024 PF102324 11/1/2024 PF110124

    Quantity: 210,960 lbs

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Source and notes

U.S. Food and Drug Administration, Enforcement Reports (openFDA food recall data) (Public domain (U.S. government work); source U.S. Food and Drug Administration, openFDA), data as of January 15, 2025.

Each week the FDA lists the recalls it has classified in its Enforcement Report, often weeks after the company announced the recall, so a month with five weekly reports tends to count more. Each recall counts once, however many products it covers, in the month FDA first listed it. Class I means the food could cause serious harm or death, Class II temporary or minor harm, and Class III is unlikely to harm anyone. Meat, poultry and most egg products are recalled by the U.S. Department of Agriculture, not the FDA, and aren't included. For what to do with a recalled product, see the FDA's recalls page.