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FDA source record Class I Terminated

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 ...

Recall Date: 2025-05-21 Recalling Firm: Reser's Fine Foods, Inc. dba Fresh Creative Foods Record Ref: H-0046-2025

FINDARECALL QUICK READ

What this record tells you

This FDA record concerns 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 ... and names Reser's Fine Foods, Inc. dba Fresh Creative Foods as the recalling firm. Use the source fields below to narrow the match, then verify the exact item and current remedy on the issuing-agency page.

  • Firm: Reser's Fine Foods, Inc. dba Fresh Creative Foods
  • Classification: Class I
  • Status: Terminated
  • Recall date: 2025-05-21
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Product Description & Identification

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.

Reason for Recall / Hazard Identified

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.

How to Check Whether Your Product Matches

A matching product name or photograph is not enough by itself. Compare every identifier available on your item or packaging with the official notice.

  1. Confirm the full product and brand or recalling-firm name.
  2. Compare package size, color, flavor, model, style, or configuration when listed.
  3. Check UPC, lot, batch, serial, date code, recall number, or USDA establishment number.
  4. Review the recall date and distribution information without assuming every seller is listed.
  5. Open the official FDA source below and follow its current instructions.

If a required identifier is missing, contact the recalling company or issuing agency through the official notice rather than guessing.

Consumer Action Recorded in the Source

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Distribution & Affected States

Distributed in MA and PA.

Verify With the Issuing Agency

This record was last updated in our index on 2026-08-09 21:59:13 UTC. Because recall enforcement statuses and instructions evolve, always verify details directly with the issuing government agency.

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Record Transparency

Issuing agency
FDA
Source ID
H-0046-2025
Indexed update
2026-08-09 21:59:13 UTC
Official source
Open issuing-agency record