Class ITerminated in FDA datasetRecall initiated Sep 26, 2025

Fresh Creative Foods (FCF) item #404736 Basil Pesto Bowtie Pasta Kit

Recalling firm: Reser's Fine Foods, Inc.

Why it was recalled

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

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Mar 31, 2026.

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ProductFresh 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.
Package size10.3125lbs

FDA code information

Use by Dates: 10/9/2025 10/10/2025 10/17/2025 10/23/2025 10/27/2025

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Full FDA record and distribution details

Original product description

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.

Original FDA recall reason

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

Recall details

Recall number
H-0089-2026
Event ID
97713
FDA status
Terminated
Initiated
Sep 26, 2025
Reported
Oct 29, 2025
Classified
Oct 17, 2025
Terminated
Mar 31, 2026
Quantity
Item #404736 = 795 cases
Location
Beaverton, OR, United States
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

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.

FDA source record · H-0089-2026

Data updated September 16, 2026. View official FDA data ↗

Follow official FDA and manufacturer guidance.