FDA Recall United States Terminated Historical recordClass I
The Kroger Co
- Product
- Smoked Mozzarella Penne Salad, packaged in plastic container…
- Published
- October 29, 2025
- Distribution
- AK, AL, AR, AZ, CA, CO, GA, ID, IL, IN,…
The Kroger Co Recall: Store-made deli items contain a pasta ingredient that was recalled due to potential Listeria monocytogenes
United States
TerminatedClass I
- Company
- The Kroger Co
- Product
- Basil Pesto Bowtie Pasta Salad, packaged in plastic containe…
- Recall date
- September 26, 2025
- Terminated
- March 6, 2026
- Source
- FDA
Reason for recall
Store-made deli items contain a pasta ingredient that was recalled due to potential Listeria monocytogenes
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Basil Pesto Bowtie Pasta Salad, packaged in plastic containers with various weights, with UPC 217573-1XXXX (sold at deli service counters) or UPC 217573-2XXXX (sold as Grab-n-Go packages in deli departments), under the banners Kroger, Baker's, City Market, Dillons, Fred Meyer, Fry's, Gerbes, King Soopers, Payless, Ralphs and Smith's | 217573-1 | 5,567.4 lbs. | Sold On: Sep 6 2025 through Oct 2 2025 |
Distribution
- AK
- AL
- AR
- AZ
- CA
- CO
- GA
- ID
- IL
- IN
- KS
- KY
- LA
- MI
- MO
- MS
- MT
- NE
- NM
- NV
- OH
- OR
- SC
- TN
- TX
- UT
- WA and WV
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- H-0094-2026
- Event ID
- 97738
- Status
- Terminated
- Classification
- Class I
- Company
- The Kroger Co
- Product description
- Basil Pesto Bowtie Pasta Salad, packaged in plastic containers with various weights, with UPC 217573-1XXXX (sold at deli service counters) or UPC 217573-2XXXX (sold as Grab-n-Go packages in deli departments), under the banners Kroger, Baker's, City Market, Dillons, Fred Meyer, Fry's, Gerbes, King Soopers, Payless, Ralphs and Smith's
- Quantity
- 5,567.4 lbs.
- Reason
- Store-made deli items contain a pasta ingredient that was recalled due to potential Listeria monocytogenes
- Recall initiation date
- September 26, 2025
- Report date
- October 29, 2025
- Classification date
- Not published in this source record
- Termination date
- March 6, 2026
- Distribution pattern
- AK, AL, AR, AZ, CA, CO, GA, ID, IL, IN, KS, KY, LA, MI, MO, MS, MT, NE, NM, NV, OH, OR, SC, TN, TX, UT, WA and WV
- UPC, lot, and code information
- UPC 217573-1; Sold On: Sep 6 2025 through Oct 2 2025
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- 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 97738 with 1 other product entry in Public Health Trace.
Responsible company: The Kroger Co
Other recalls from The Kroger Co
FDA Recall United States Terminated Historical recordClass I
The Kroger Co
- Product
- Smoked Mozzarella Penne Salad, packaged in plastic container…
- Published
- October 29, 2025
- Distribution
- AK, AL, AR, AZ, CA, CO, GA, ID, IL, IN,…
FDA Recall United States Terminated Historical recordClass I
The Kroger Co
- Product
- BOAR'S HEAD HUMMUS VEG PLATTER MED, 5 lb., packaged in a pla…
- Published
- January 22, 2025
- Distribution
- Multiple states
FDA Recall United States Terminated Historical recordClass I
The Kroger Co
- Product
- BOAR'S HEAD HUMMUS VEG PLATTER SM, 2.5 lb., packaged in a pl…
- Published
- January 22, 2025
- Distribution
- Multiple states
A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| State | Distributed |
|---|---|
| Alaska | 1 |
| Alabama | 1 |
| Arkansas | 1 |
| Arizona | 1 |
| California | 1 |
| Colorado | 1 |
| Georgia | 1 |
| Idaho | 1 |
| Illinois | 1 |
| Indiana | 1 |
| Kansas | 1 |
| Kentucky | 1 |
| Louisiana | 1 |
| Michigan | 1 |
| Missouri | 1 |
| Mississippi | 1 |
| Montana | 1 |
| Nebraska | 1 |
| New Mexico | 1 |
| Nevada | 1 |
| Ohio | 1 |
| Oregon | 1 |
| South Carolina | 1 |
| Tennessee | 1 |
| Texas | 1 |
| Utah | 1 |
| Washington | 1 |
| West Virginia | 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.
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Technical source data
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.
What should I do if I have this product?
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.
Where can I find more official information?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.
