Fresh Creative Foods (FCF) item #404637 Basil Pesto Bowtie Pasta Kit Item V, UPC#13454 38053. Perishable/Refrigerated product. Net wt. 10.5625lbs. This kit contains 2/3lbs. sealed bags of affected Bowtie Pasta, and it is not sold directly to consumers.

Class I - Dangerous
Recalled: September 26, 2025 Reser's Fine Foods Other Foods

What Should You Do?

  1. Check if you have this product:
    Use by Dates: 9/13/2025 9/16/2025 9/18/2025 9/19/2025 9/20/2025 9/21/2025 9/23/2025 9/24/2025 9/25/2025 9/26/2025 9/27/2025 9/28/2025 9/29/2025 9/30/2025 10/1/2025 10/2/2025 10/3/2025 10/4/2025
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
Reser's Fine Foods, Inc.
Reason for Recall:
Salad Kits are recalled due to potential contamination with Listeria monocytogenes.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
ongoing

Product Information

Full Description:

Fresh Creative Foods (FCF) item #404637 Basil Pesto Bowtie Pasta Kit Item V, UPC#13454 38053. Perishable/Refrigerated product. Net wt. 10.5625lbs. This kit contains 2/3lbs. sealed bags of affected Bowtie Pasta, and it is not sold directly to consumers.

Product Codes/Lot Numbers:

Use by Dates: 9/13/2025 9/16/2025 9/18/2025 9/19/2025 9/20/2025 9/21/2025 9/23/2025 9/24/2025 9/25/2025 9/26/2025 9/27/2025 9/28/2025 9/29/2025 9/30/2025 10/1/2025 10/2/2025 10/3/2025 10/4/2025

Distribution:

Distributed in: AZ, CA, CO, UT, WA, TX, FL, GA, IN, MD, MO, OR, PA

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: H-0090-2026

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