Pepperjack Cheese Burger, Dakota Toms brand, Net Wt 5.7 oz, individual pre-packaged components in MEP packaging, UPC 737
Summary
The FDA issued a Class I for Pepperjack Cheese Burger, Dakota Toms brand, Net Wt 5.7 oz, individual pre-packa by Dakota Tom's, Inc. Reason: Potential Listeria monocytogenes contamination.
Details
Source
Food Recall
External ID
F-0127-2025
Action Date
2024-11-06
Status
Terminated
Category
food
Product Description
Pepperjack Cheese Burger, Dakota Toms brand, Net Wt 5.7 oz, individual pre-packaged components in MEP packaging, UPC 737296806008
Lot/Code Info: Expiration date: 9/1/24 - 11/28/24
Quantity Affected: 520 sandwiches
Reason for Recall
Potential Listeria monocytogenes contamination
Distribution
U.S. distribution within states in retail locations in ND, SD, WY, IA, MN. No Foreign distribution.
Type: Voluntary: Firm initiated
Recall Initiated: 2024-10-11
Company
Corsica, SD
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 42 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Dakota Tom's, Inc has 4 FDA actions in our database, including 4 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 (Dakota Tom's, Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Dakota Tom's, Inc have FDA actions?
Dakota Tom's, Inc has 4 FDA actions in our database, including 4 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0127-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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