Lancaster LF Authentic Greek Salad Kit, 2/7.125lb. packages, net wt. 14.25lb., Item Code 407079, UPC 13454.38482. Thi
Summary
The FDA issued a Class I for Lancaster LF Authentic Greek Salad Kit, 2/7.125lb. packages, net wt. 14.25lb., I by Reser's Fine Foods, Inc. dba Fresh Creative Foods. Reason: Salmonella. Greek Salad Kit made with recalled cucumbers sourced from Bedner Grower's Company which may be contaminated with Salmonella and implicated.
Details
Source
Food Recall
External ID
H-0046-2025
Action Date
2025-06-25
Status
Terminated
Category
food
Product Description
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.
Lot/Code Info: Use by dates of 05/30/25, 05/31/25, 06/02/25, and 06/03/25.
Quantity Affected: 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.
Distribution
Distributed in MA and PA.
Type: Voluntary: Firm initiated
Recall Initiated: 2025-05-21
Company
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 56 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
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 (Reser's Fine Foods, Inc. dba Fresh Creative Foods) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Reser's Fine Foods, Inc. dba Fresh Creative Foods have FDA actions?
This is the only FDA action we have on record for Reser's Fine Foods, Inc. dba Fresh Creative Foods in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0046-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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