RecallHawk
Class I Recall

1. Freshness Guaranteed Peanut Butter Snack Mix, Net Wt 12oz, UPC 78742 03912, 8/12oz case 2. Peanut Butter Snack Mix, N

Palmer & Company

Summary

The FDA issued a Class I for 1. Freshness Guaranteed Peanut Butter Snack Mix, Net Wt 12oz, UPC 78742 03912, 8 by Palmer & Company. Reason: Potential salmonella contamination.

Details

Source

Food Recall

External ID

F-1670-2024

Action Date

2024-08-14

Status

Terminated

Category

food

Product Description

1. Freshness Guaranteed Peanut Butter Snack Mix, Net Wt 12oz, UPC 78742 03912, 8/12oz case 2. Peanut Butter Snack Mix, Net Wt 4.5oz to go container, Distributed by: Kwik Trip Inc; UPC 39779 00424, 12/4.5oz case

Lot/Code Info: 1. Best by dates: 11/13/24 - 12/22/24 2. Best by date: 1/18/25

Reason for Recall

Potential salmonella contamination

Distribution

Nationwide United States and Canada

Type: Voluntary: Firm initiated

Recall Initiated: 2024-05-03

Company

Palmer & Company

Sioux City, IA

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 200 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Palmer & Company has 18 FDA actions in our database, including 18 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 (Palmer & Company) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Palmer & Company have FDA actions?

Palmer & Company has 18 FDA actions in our database, including 18 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1670-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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