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Salad Kits are recalled due to potential contamination with Listeria monocytogenes.
- Recall initiated
- Reported by source
- Recall terminated
Recalled products
Product description
UPC
Quantity
Lot / code information
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.
Not published in this source record
Item #404736 = 795 cases
Use by Dates: 10/9/2025 10/10/2025 10/17/2025 10/23/2025 10/27/2025
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.
Official source record
Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
H-0089-2026
Event ID
97713
Status
Terminated
Classification
Class I
Company
Reser's Fine Foods, Inc.
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.
Quantity
Item #404736 = 795 cases
Reason
Salad Kits are recalled due to potential contamination with Listeria monocytogenes.
Recall initiation date
September 26, 2025
Report date
October 29, 2025
Classification date
Not published in this source record
Termination date
March 31, 2026
Distribution pattern
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.
UPC, lot, and code information
Use by Dates: 10/9/2025 10/10/2025 10/17/2025 10/23/2025 10/27/2025
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date
Other products recalled under this same event
This recall shares FDA event ID 97713 with 2 other product
entries in Public Health Trace.
FDA Recall🇺🇸 United StatesTerminatedTerminated: March 31, 2026Historical recordClass I
A map highlighting the states named in the source's distribution description.
Distributed
No data published
Shading reflects state-level totals only, as published by the source. It does not imply
county-level or point-level precision.
Distribution map
State
Distributed
Arizona
1
California
1
Colorado
1
Utah
1
Washington
1
Texas
1
Florida
1
Georgia
1
Indiana
1
Maryland
1
Missouri
1
Oregon
1
Pennsylvania
1
States shown are extracted from the source's free-text distribution description above; a narrative
description (e.g. "distributed nationwide") may not list individual states to extract.
View raw source data
-- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class I mean?
A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.
Is this recall still active?
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
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Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
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or product is unsafe beyond what the official source has published.
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