Class ITerminatedVoluntary: Firm initiated
F&S Produce West LLC: food recall F-0271-2025
F&S Produce West LLC of Riverside, CA recalled Mediterranean Inspired Party Tray; Sell by dates 11/27/2024- 12/11/2024 UPC: 826766145966; Perishable, Keep Refrigerated. Reason: Mediterranean party tray contains tzatziki sauce made with potentially contaminated (Salmonella) cucumbers. The FDA listed it as Class I in its Enforcement Report dated Dec 18, 2024; distribution: Arizona, California, Idaho, Montana, Nevada, Utah, Wyoming.
Record status as published: Terminated (terminated Apr 1, 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
- Mediterranean Inspired Party Tray; Sell by dates 11/27/2024- 12/11/2024 UPC: 826766145966; Perishable, Keep Refrigerated
- Product quantity
- 1,024 consumer units
- Reason for recall
- Mediterranean party tray contains tzatziki sauce made with potentially contaminated (Salmonella) cucumbers.
- Codes, lots and dates on the package
- Sell by dates 11/27/2024- 12/11/2024
- Distribution pattern
- 187 retail locations in AZ, CA, ID, MT, NV, UT, WY
- Recalling firm
- F&S Produce West LLC, Riverside, CA
- Classification
- Class I — the FDA uses this class for a situation in which there is a reasonable probability that using or being exposed to the product will cause serious adverse health consequences or death.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Dec 5, 2024 |
| Classified by the FDA | Dec 11, 2024 |
| Published in the Enforcement Report | Dec 18, 2024 |
| Terminated | Apr 1, 2025 |
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number F-0271-2025 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
- Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service. The FDA does not endorse OpenPlate.