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FDA source record Class I Terminated

Fresh Creative Foods (FCF) item #404736 Basil Pesto Bowtie Pasta Kit, UPC #13454 38092. Perishable/Refrigerated product. Net wt. 10.3125lbs. This kit contains 2/3lb. sealed bags...

Recall Date: 2025-09-26 Recalling Firm: Reser's Fine Foods, Inc. Record Ref: H-0089-2026

FINDARECALL QUICK READ

What this record tells you

This FDA record concerns Fresh Creative Foods (FCF) item #404736 Basil Pesto Bowtie Pasta Kit, UPC #13454 38092. Perishable/Refrigerated product. Net wt. 10.3125lbs. This kit contains 2/3lb. sealed bags... and names Reser's Fine Foods, Inc. 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.
  • Classification: Class I
  • Status: Terminated
  • Recall date: 2025-09-26
Best identifiers to check for a FDA record

Compare UPC/GTIN, lot or batch code, package size, flavor or variety, and any best-by/use-by date listed in the notice.

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Product Description & Identification

Fresh Creative Foods (FCF) item #404736 Basil Pesto Bowtie Pasta Kit, UPC #13454 38092. Perishable/Refrigerated product. Net wt. 10.3125lbs. This kit contains 2/3lb. sealed bags of affected Bowtie Pasta and does not contain spinach. Kit is not sold directly to consumers.

Reason for Recall / Hazard Identified

Salad Kits are recalled due to potential contamination with Listeria monocytogenes.

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

Item #404736 was distributed in AZ, CA, CO, UT, and WA. Item #404637 was distributed in AZ, CA, CO, and TX. Item #404284 was distributed in AZ, CA, CO, FL, GA, IN, MD, MO, OR, PA, TX, UT, and WA.

Verify With the Issuing Agency

This record was last updated in our index on 2026-08-09 21:59:12 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-0089-2026
Indexed update
2026-08-09 21:59:12 UTC
Official source
Open issuing-agency record