Food FDA Class I Terminated Pathogen contamination
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
Reser's Fine Foods, Inc. dba Fresh Creative Foods Published Jun 25, 2025
Risk level
Class IDangerous or defective — could cause serious health problems or death.
Severity score 90/100
What should you do?
- Check whether you have this product, using the lot codes, UPCs, and dates listed below.
- Do not eat, serve, or sell the affected product.
- Return it to the place of purchase for a refund, or throw it away in a sealed bag so people and animals can’t get to it.
- Contact Reser's Fine Foods, Inc. dba Fresh Creative Foods or your place of purchase with questions, and see the source record below for full details.
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.
Hazards
Salmonella · primary
Affected products (1)
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.
123 kits
Code info: Use by dates of 05/30/25, 05/31/25, 06/02/25, and 06/03/25.
Affected areas
MassachusettsPennsylvania
Timeline
- InitiatedMay 21, 2025
- PublishedJun 25, 2025
- TerminatedMar 19, 2026
- Recall number
- H-0046-2025
- Agency
- U.S. Food and Drug Administration
- Country
- US
FDA records come from the openFDA food enforcement-report dataset — the agency's full weekly enforcement list. Most entries are not issued as consumer press releases, so they won't appear on fda.gov/recalls or in a web search. The source record link above resolves this exact recall by its number.