RecallHawk
Class I Recall

PLANTERS¿ Deluxe Lightly Salted Mixed Nuts 8.75 oz. UPC 2900001621. Packaged in a metal corrugate can with plastic lid.

Hormel Foods Corporation

Summary

The FDA issued a Class I for PLANTERS¿ Deluxe Lightly Salted Mixed Nuts 8.75 oz. UPC 2900001621. Packaged in by Hormel Foods Corporation. Reason: Possible contamination with Listeria monocytogenes.

Details

Source

Food Recall

External ID

F-1287-2024

Action Date

2024-06-12

Status

Terminated

Category

food

Product Description

PLANTERS¿ Deluxe Lightly Salted Mixed Nuts 8.75 oz. UPC 2900001621. Packaged in a metal corrugate can with plastic lid. 12 cans per case.

Lot/Code Info: 05APR26

Quantity Affected: 567 cases - 6804 cans

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

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-1287-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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