Dakota Tom's and Market Fresh branded Chicken Salad Croissant sandwiches. Net Wt. 6.5 oz. UPC 37296-10100, Dakota Toms,
Summary
The FDA issued a Class I for Dakota Tom's and Market Fresh branded Chicken Salad Croissant sandwiches. Net W by Dakota Tom's, Inc. Reason: Sandwiches contain undeclared egg and milk..
Details
Source
Food Recall
External ID
F-0350-2022
Action Date
2021-12-29
Status
Terminated
Category
food
Product Description
Dakota Tom's and Market Fresh branded Chicken Salad Croissant sandwiches. Net Wt. 6.5 oz. UPC 37296-10100, Dakota Toms, Box 271, Corsica, SD 57328.
Lot/Code Info: Sandwiches dated 12/7/2021 thru 1/12/2022
Quantity Affected: 2000 sandwiches
Reason for Recall
Sandwiches contain undeclared egg and milk.
Distribution
IA, MN, ND, SD
Type: Voluntary: Firm initiated
Recall Initiated: 2021-12-07
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 75 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-0350-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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