C.H. Guenther & Son, Inc. Recall: Undeclared egg allergen

🇺🇸 United States

1. December 10, 2024 - Recall initiated
2. January 15, 2025 - Reported by source
3. February 21, 2025 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0384-2025

Event ID

95965

Status

Terminated

Classification

Class I

Company

C.H. Guenther & Son, Inc.

Product description

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

Quantity

210,960 lbs

Reason

Undeclared egg allergen

Recall initiation date

December 10, 2024

Report date

January 15, 2025

Classification date

Not published in this source record

Termination date

February 21, 2025

Distribution pattern

Louisiana, Tennessee, Texas, Oklahoma, Arkansas, Missouri, Florida, Virginia

UPC, lot, and code information

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

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

Letter

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Responsible company: C.H. Guenther & Son, Inc.

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: July 18, 2026 ET

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.

• Email
• X / Twitter
• Facebook