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