RecallHawk
Class II Recall

Lunds & Byerlys lone star dip. Net Wt 12 oz. (340.5g) UPC 0 18169-74197 9. Produced by Lunds & Byerlys, Edina, MN 55

Lund Food Holdings Inc

Summary

The FDA issued a Class II for Lunds & Byerlys lone star dip. Net Wt 12 oz. (340.5g) UPC 0 18169-74197 9. Pr by Lund Food Holdings Inc. Reason: Potential mold contamination..

Details

Source

Food Recall

External ID

F-0052-2025

Action Date

2024-10-23

Status

Terminated

Category

food

Product Description

Lunds & Byerlys lone star dip. Net Wt 12 oz. (340.5g) UPC 0 18169-74197 9. Produced by Lunds & Byerlys, Edina, MN 55424.

Lot/Code Info: Lot Code: 20240826, Use By: 10/15/24 Lot Code: 20240828, 20240829, Use By: 10/17/24

Quantity Affected: 756 units

Reason for Recall

Potential mold contamination.

Distribution

MN

Type: Voluntary: Firm initiated

Recall Initiated: 2024-09-27

Company

Lund Food Holdings Inc

Eden Prairie, MN

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

This was one of 33 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Lund Food Holdings Inc has 2 FDA actions in our database, including 2 recalls.

Frequently Asked Questions

What is a Class II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

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 (Lund Food Holdings Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Lund Food Holdings Inc have FDA actions?

Lund Food Holdings Inc 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-0052-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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