RecallHawk
Class I Recall

Kroger Collard Greens packaged in plastic 16oz bag - 8 bags per case

The Kroger Co

Summary

The FDA issued a Class I for Kroger Collard Greens packaged in plastic 16oz bag - 8 bags per case by The Kroger Co. Reason: Potential contamination of Listeria monocytogenes.

Details

Source

Food Recall

External ID

F-0300-2024

Action Date

2023-11-01

Status

Terminated

Category

food

Product Description

Kroger Collard Greens packaged in plastic 16oz bag - 8 bags per case

Lot/Code Info: Lot No. 110093-387 UPC 11110-18171 Best By 10-16-23

Quantity Affected: 458 cases (3664 retail units)

Reason for Recall

Potential contamination of Listeria monocytogenes

Distribution

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

Type: Voluntary: Firm initiated

Recall Initiated: 2023-10-19

Company

The Kroger Co

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 16 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 "F-0300-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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