Smoked Mozzarella Penne Salad, packaged in plastic containers with various weights, with UPC 227573-1XXXX (sold at deli
Summary
The FDA issued a Class I for Smoked Mozzarella Penne Salad, packaged in plastic containers with various weigh by The Kroger Co. Reason: Store-made deli items contain a pasta ingredient that was recalled due to potential Listeria monocytogenes.
Details
Source
Food Recall
External ID
H-0095-2026
Action Date
2025-10-29
Status
Terminated
Category
food
Product Description
Smoked Mozzarella Penne Salad, packaged in plastic containers with various weights, with UPC 227573-1XXXX (sold at deli service counters) or UPC 227573-2XXXX (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
Lot/Code Info: Sold On: Aug 29 2025 through Oct 2 2025
Quantity Affected: 25,792 lbs.
Reason for Recall
Store-made deli items contain a pasta ingredient that was recalled due to potential Listeria monocytogenes
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
Type: Voluntary: Firm initiated
Recall Initiated: 2025-09-26
Company
Cincinnati, OH
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.
The Kroger Co has 29 FDA actions in our database, including 29 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 (The Kroger Co) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does The Kroger Co have FDA actions?
The Kroger Co has 29 FDA actions in our database, including 29 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0095-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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