Fresh Creative Foods (FCF) item #404736 Basil Pesto Bowtie Pasta Kit, UPC #13454 38092. Perishable/Refrigerated product.
Summary
The FDA issued a Class I for Fresh Creative Foods (FCF) item #404736 Basil Pesto Bowtie Pasta Kit, UPC #13454 by Reser's Fine Foods, Inc.. Reason: Salad Kits are recalled due to potential contamination with Listeria monocytogenes..
Details
Source
Food Recall
External ID
H-0089-2026
Action Date
2025-10-29
Status
Terminated
Category
food
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.
Lot/Code Info: Use by Dates: 10/9/2025 10/10/2025 10/17/2025 10/23/2025 10/27/2025
Quantity Affected: Item #404736 = 795 cases
Reason for Recall
Salad Kits are recalled due to potential contamination with Listeria monocytogenes.
Distribution
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.
Type: Voluntary: Firm initiated
Recall Initiated: 2025-09-26
Company
Beaverton, OR
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 91 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Reser's Fine Foods, Inc. has 62 FDA actions in our database, including 62 recalls.
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.) 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. have FDA actions?
Reser's Fine Foods, Inc. has 62 FDA actions in our database, including 62 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0089-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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