Keith Valley mustard, net 1 gal, Distributed by: Ben E Keith Food Ft Worth, TX, UPC 046045062467; Red Boy brand mustard,
Summary
The FDA issued a Class III for Keith Valley mustard, net 1 gal, Distributed by: Ben E Keith Food Ft Worth, TX, by Clements Foods Co. Reason: Ingredient (mustard seeds) tested positive for Salmonella.
Details
Source
Food Recall
External ID
F-0457-2025
Action Date
2025-02-05
Status
Terminated
Category
food
Product Description
Keith Valley mustard, net 1 gal, Distributed by: Ben E Keith Food Ft Worth, TX, UPC 046045062467; Red Boy brand mustard, Net 1 GAL., Distributed by Clements Food Company Oklahoma City, OK 73116, UPC 071735128154
Lot/Code Info: 4341CF, 4342CF, 4343CF, 4344CF, 4346CF; CF4341, CF4342, CF4344, CF4346
Quantity Affected: 96 cases of Keith Valley, 864 cases of Red Boy
Reason for Recall
Ingredient (mustard seeds) tested positive for Salmonella
Distribution
Distributed to customers in KS, TX, OK, AR
Type: Voluntary: Firm initiated
Recall Initiated: 2024-12-17
Company
Oklahoma City, OK
Context & Analysis
This is a Class III recall. Class III recalls involve products unlikely to cause adverse health consequences, but that violate FDA regulations.
This was one of 47 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Frequently Asked Questions
What is a Class III recall?
A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.
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 (Clements Foods Co) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Clements Foods Co have FDA actions?
This is the only FDA action we have on record for Clements Foods Co in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0457-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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