Class IIITerminatedVoluntary: Firm initiated
Clements Foods Co: food recall F-0457-2025
Clements Foods Co of Oklahoma City, OK recalled Keith Valley mustard, net 1 gal, Distributed by: Ben E Keith Food Ft Worth, TX, UPC 046045062467; Red Boy brand… Reason: Ingredient (mustard seeds) tested positive for Salmonella. The FDA listed it as Class III in its Enforcement Report dated Feb 5, 2025; distribution: Arkansas, Kansas, Oklahoma, Texas.
Record status as published: Terminated (terminated Feb 28, 2025). openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- Product
- 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
- Product quantity
- 96 cases of Keith Valley, 864 cases of Red Boy
- Reason for recall
- Ingredient (mustard seeds) tested positive for Salmonella
- Codes, lots and dates on the package
- 4341CF, 4342CF, 4343CF, 4344CF, 4346CF; CF4341, CF4342, CF4344, CF4346
- Distribution pattern
- Distributed to customers in KS, TX, OK, AR
- Recalling firm
- Clements Foods Co, Oklahoma City, OK
- Classification
- Class III — the FDA uses this class for a situation in which using or being exposed to the product is not likely to cause adverse health consequences.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
- Telephone
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Dec 17, 2024 |
| Classified by the FDA | Jan 30, 2025 |
| Published in the Enforcement Report | Feb 5, 2025 |
| Terminated | Feb 28, 2025 |
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number F-0457-2025 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
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