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