235214 Baker's Source Traditional Cornbread Mix Complete, 5 LB Bags, 30 LB Cases Foodservice Use, Human Consumption & mi
Summary
The FDA issued a Class I for 235214 Baker's Source Traditional Cornbread Mix Complete, 5 LB Bags, 30 LB Cases by C.H. Guenther & Son, Inc.. Reason: Undeclared egg allergen.
Details
Source
Food Recall
External ID
F-0384-2025
Action Date
2025-01-15
Status
Terminated
Category
food
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
Lot/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
Quantity Affected: 210,960 lbs
Reason for Recall
Undeclared egg allergen
Distribution
Louisiana, Tennessee, Texas, Oklahoma, Arkansas, Missouri, Florida, Virginia
Type: Voluntary: Firm initiated
Recall Initiated: 2024-12-10
Company
San Antonio, 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 69 food recalls issued in the same week, part of 204 food-related FDA actions this month.
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 (C.H. Guenther & Son, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does C.H. Guenther & Son, Inc. have FDA actions?
This is the only FDA action we have on record for C.H. Guenther & Son, Inc. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0384-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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