Skip to content
Back to recalls
Food FDA Class I Terminated Undeclared allergen

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

C.H. Guenther & Son, Inc. Published Jan 15, 2025

Risk level

Class I

Dangerous or defective — could cause serious health problems or death.

Severity score 87/100

What should you do?

  • Check whether you have this product, using the lot codes, UPCs, and dates listed below.
  • If you are allergic or sensitive to the ingredient noted, do not eat it — it could cause a serious reaction.
  • Return it to the place of purchase for a refund, or throw it away in a sealed bag so people and animals can’t get to it.
  • Contact C.H. Guenther & Son, Inc. or your place of purchase with questions, and see the source record below for full details.
Reason for recall

Undeclared egg allergen

Hazards

Egg · primary

Affected products (1)

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

210,960 lbs

Lot codes: Codes
Code info: 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

Affected areas

ArkansasFloridaLouisianaMissouriOklahomaTennesseeTexasVirginia

Timeline

  1. Initiated
    Dec 10, 2024
  2. Published
    Jan 15, 2025
  3. Terminated
    Feb 21, 2025
Recall number
F-0384-2025
Agency
U.S. Food and Drug Administration
Country
US
Source data (openFDA JSON) About FDA enforcement reports

FDA records come from the openFDA food enforcement-report dataset — the agency's full weekly enforcement list. Most entries are not issued as consumer press releases, so they won't appear on fda.gov/recalls or in a web search. The source record link above resolves this exact recall by its number.