Class ITerminatedVoluntary: Firm initiated
Reser's Fine Foods, Inc. dba Fresh Creative Foods: food recall H-0046-2025
Reser's Fine Foods, Inc. dba Fresh Creative Foods of Vista, CA recalled Lancaster LF Authentic Greek Salad Kit, 2/7.125lb. packages, net wt. 14.25lb., Item Code 407079, UPC 13454.38482. This… Reason: Salmonella. Greek Salad Kit made with recalled cucumbers sourced from Bedner Grower's Company which may be contaminated with Salmonella and implicated in an ongoing outbreak. The FDA listed it as Class I in its Enforcement Report dated Jun 25, 2025; distribution: Massachusetts, Pennsylvania.
Record status as published: Terminated (terminated Mar 19, 2026). 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
- Lancaster LF Authentic Greek Salad Kit, 2/7.125lb. packages, net wt. 14.25lb., Item Code 407079, UPC 13454.38482. This is wholesale kit consisting of pre-packaged components in a corrugated box for assembly by retail delis. Kit contains sealed bags of cut produce (sliced cucumber, red bell pepper, green bell pepper, red onions), grape tomatoes, whole Kalamata olives, Feta cheese, and Greek Vinaigrette dressing.
- Product quantity
- 123 kits
- Reason for recall
- Salmonella. Greek Salad Kit made with recalled cucumbers sourced from Bedner Grower's Company which may be contaminated with Salmonella and implicated in an ongoing outbreak.
- Codes, lots and dates on the package
- Use by dates of 05/30/25, 05/31/25, 06/02/25, and 06/03/25.
- Distribution pattern
- Distributed in MA and PA.
- Recalling firm
- Reser's Fine Foods, Inc. dba Fresh Creative Foods, Vista, 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 | May 21, 2025 |
| Classified by the FDA | Jun 16, 2025 |
| Published in the Enforcement Report | Jun 25, 2025 |
| Terminated | Mar 19, 2026 |
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-0046-2025 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
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