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: The firm was notified by their manufacturer that the product is contaminated with Listeria monocytogenes.
United States
TerminatedClass I
- Company
- The Kroger Co
- Product
- Chicken Salad Sandwich 6.8 oz plastic container Contains: Wh…
- Recall date
- September 22, 2017
- Terminated
- December 28, 2017
- Source
- FDA
Reason for recall
The firm was notified by their manufacturer that the product is contaminated with Listeria monocytogenes.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Chicken Salad Sandwich 6.8 oz plastic container Contains: Wheat, Egg, Soy USPC 6 63209-02050 9 | Not published in this source record | 2,634 sandwiches | Sell By dates: 09/20/2017 - 09/28/2017 |
Distribution
- Product was shipped to the following states: CO
- NM
- UT & WY.
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0027-2018
- Event ID
- 78178
- Status
- Terminated
- Classification
- Class I
- Company
- The Kroger Co
- Product description
- Chicken Salad Sandwich 6.8 oz plastic container Contains: Wheat, Egg, Soy USPC 6 63209-02050 9
- Quantity
- 2,634 sandwiches
- Reason
- The firm was notified by their manufacturer that the product is contaminated with Listeria monocytogenes.
- Recall initiation date
- September 22, 2017
- Report date
- October 25, 2017
- Classification date
- Not published in this source record
- Termination date
- December 28, 2017
- Distribution pattern
- Product was shipped to the following states: CO, NM, UT & WY.
- UPC, lot, and code information
- Sell By dates: 09/20/2017 - 09/28/2017
- 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
Responsible company: The Kroger Co
Other recalls from The Kroger Co
FDA Recall United States Terminated Historical recordClass I
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- Product
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- Published
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- Distribution
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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
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 |
|---|---|
| Colorado | 1 |
| New Mexico | 1 |
| Utah | 1 |
| Wyoming | 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.
