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The Kroger Co Recall: Potential contamination of Listeria monocytogenes

United States

TerminatedClass I

Company
The Kroger Co
Product
Kroger Collard Greens packaged in plastic 16oz bag - 8 bags…
Recall date
October 19, 2023
Terminated
November 14, 2023
Source
FDA

Reason for recall

Potential contamination of Listeria monocytogenes

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Kroger Collard Greens packaged in plastic 16oz bag - 8 bags per case Not published in this source record 458 cases (3664 retail units) Lot No. 110093-387 UPC 11110-18171 Best By 10-16-23

Distribution

  • Alabama
  • Arkansas
  • Georgia
  • Kentucky
  • Mississippi
  • South Carolina
  • Tennessee
  • Illinois
  • Indiana and Missouri

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0300-2024
Event ID
93283
Status
Terminated
Classification
Class I
Company
The Kroger Co
Product description
Kroger Collard Greens packaged in plastic 16oz bag - 8 bags per case
Quantity
458 cases (3664 retail units)
Reason
Potential contamination of Listeria monocytogenes
Recall initiation date
October 19, 2023
Report date
November 1, 2023
Classification date
Not published in this source record
Termination date
November 14, 2023
Distribution pattern
Alabama, Arkansas, Georgia, Kentucky, Mississippi, South Carolina, Tennessee, Illinois, Indiana and Missouri
UPC, lot, and code information
Lot No. 110093-387 UPC 11110-18171 Best By 10-16-23
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
E-Mail
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: The Kroger Co

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Distribution
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Product
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Published
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Distribution
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Product
BOAR'S HEAD HUMMUS VEG PLATTER MED, 5 lb., packaged in a pla…
Published
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Distribution
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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.