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 that the product was manufactured with an ingredient that may contain low levels of peanut reside which is not declared in the ingredient statement.
United States
TerminatedClass II
- Company
- The Kroger Co
- Product
- Kroger DELUXE ICE CREAM S'MORES 48 FL OZ (1.5 QT) 1.4 ML ING…
- Recall date
- June 15, 2016
- Terminated
- January 8, 2018
- Source
- FDA
Reason for recall
The firm was notified that the product was manufactured with an ingredient that may contain low levels of peanut reside which is not declared in the ingredient statement.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Kroger DELUXE ICE CREAM S'MORES 48 FL OZ (1.5 QT) 1.4 ML INGREDIENTS: ICE CREAM***GRAHAM COOKIES***CHOCOLATE CHUNKS***CONTAINS: MILK, SOY, WHEAT, COCONUT. UPC 0 11110 01399 6 DISTRIBUTED BY THE KROGER CO. CINCINNATI, OHIO 45202 | Not published in this source record | Not published in this source record | Not published in this source record |
Distribution
- Product was shipped to the following states: AK
- AL
- AR
- AZ
- CA
- CO
- GA
- ID
- IL
- IN
- KS
- KY
- MI
- MO
- MT
- MS
- NC
- NE
- NM
- NV
- OH
- OR
- SC
- TN
- UT
- VA
- WA
- WV & WY.
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-1873-2016
- Status
- Terminated
- Classification
- Class II
- Company
- The Kroger Co
- Product description
- Kroger DELUXE ICE CREAM S'MORES 48 FL OZ (1.5 QT) 1.4 ML INGREDIENTS: ICE CREAM***GRAHAM COOKIES***CHOCOLATE CHUNKS***CONTAINS: MILK, SOY, WHEAT, COCONUT. UPC 0 11110 01399 6 DISTRIBUTED BY THE KROGER CO. CINCINNATI, OHIO 45202
- Quantity
- Not published in this source record
- Reason
- The firm was notified that the product was manufactured with an ingredient that may contain low levels of peanut reside which is not declared in the ingredient statement.
- Recall initiation date
- June 15, 2016
- Report date
- August 10, 2016
- Classification date
- Not published in this source record
- Termination date
- January 8, 2018
- Distribution pattern
- Product was shipped to the following states: AK, AL, AR, AZ, CA, CO, GA, ID, IL, IN, KS, KY, MI, MO, MT, MS, NC, NE, NM, NV, OH, OR, SC, TN, UT, VA, WA, WV & WY.
- UPC, lot, and code information
- Not published in this source record
- Voluntary or mandated
- Not published in this source record
- Initial notification method
- Not published in this source record
- 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
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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
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- 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 |
| Michigan | 1 |
| Missouri | 1 |
| Montana | 1 |
| Mississippi | 1 |
| North Carolina | 1 |
| Nebraska | 1 |
| New Mexico | 1 |
| Nevada | 1 |
| Ohio | 1 |
| Oregon | 1 |
| South Carolina | 1 |
| Tennessee | 1 |
| Utah | 1 |
| Virginia | 1 |
| Washington | 1 |
| West Virginia | 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 II mean?
A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.
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.
