RecallHawk
Class I Recall

BOAR'S HEAD HUMMUS VEG PLATTER SM, 2.5 lb., packaged in a plastic container with a plastic lid, UPC 42421-61545

The Kroger Co

Summary

The FDA issued a Class I for BOAR'S HEAD HUMMUS VEG PLATTER SM, 2.5 lb., packaged in a plastic container with by The Kroger Co. Reason: Platters and trays prepared in-store may contain cut cucumbers that were previously recalled due to potential contamination with Salmonella..

Details

Source

Food Recall

External ID

F-0389-2025

Action Date

2025-01-22

Status

Terminated

Category

food

Product Description

BOAR'S HEAD HUMMUS VEG PLATTER SM, 2.5 lb., packaged in a plastic container with a plastic lid, UPC 42421-61545

Lot/Code Info: All lot codes

Quantity Affected: 11 units

Reason for Recall

Platters and trays prepared in-store may contain cut cucumbers that were previously recalled due to potential contamination with Salmonella.

Distribution

AZ, CO, LA, NM, TX, UT, WY

Type: Voluntary: Firm initiated

Recall Initiated: 2024-11-29

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 29 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-0389-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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