PLANTERS¿ Honey Roasted Peanuts 4oz UPC 2900002097. Packaged in a flexible film package. 12 packages per case.
Summary
The FDA issued a Class I for PLANTERS¿ Honey Roasted Peanuts 4oz UPC 2900002097. Packaged in a flexible film by Hormel Foods Corporation. Reason: Possible contamination with Listeria monocytogenes.
Details
Source
Food Recall
External ID
F-1288-2024
Action Date
2024-06-12
Status
Terminated
Category
food
Product Description
PLANTERS¿ Honey Roasted Peanuts 4oz UPC 2900002097. Packaged in a flexible film package. 12 packages per case.
Lot/Code Info: 04 11 25
Quantity Affected: 1261 cases - 15,132 packages
Reason for Recall
Possible contamination with Listeria monocytogenes
Distribution
Distributed to distribution centers in FL, GA, AL, NC, and SC.
Type: Voluntary: Firm initiated
Recall Initiated: 2024-05-02
Company
Suffolk, VA
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 77 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Hormel Foods Corporation has 2 FDA actions in our database, including 2 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 (Hormel Foods Corporation) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Hormel Foods Corporation have FDA actions?
Hormel Foods Corporation has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1288-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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