Hy-Vee To Go Cookies & Cream Mix, Net wt. 4 oz (113g), UPC 0075450486740, 6 containers per case. Hy-Vee Cookies & Cream
Summary
The FDA issued a Class I for Hy-Vee To Go Cookies & Cream Mix, Net wt. 4 oz (113g), UPC 0075450486740, 6 cont by Hy-Vee Stores Inc. Reason: Potential Salmonella contamination.
Details
Source
Food Recall
External ID
F-1304-2024
Action Date
2024-06-05
Status
Terminated
Category
food
Product Description
Hy-Vee To Go Cookies & Cream Mix, Net wt. 4 oz (113g), UPC 0075450486740, 6 containers per case. Hy-Vee Cookies & Cream Mix, Net Wt. 16oz (453g), UPC 0075450486730, 6 containers per case.
Lot/Code Info: Lot numbers 24073, 24101, and 24117
Quantity Affected: 154 cases (6 x 4oz containers); 619 cases (6 x 16oz containers)
Reason for Recall
Potential Salmonella contamination
Distribution
IA, IL, KS, MN, MO, NE, SD, WI
Type: Voluntary: Firm initiated
Recall Initiated: 2024-05-06
Company
West Des Moines, 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 38 food recalls issued in the same week, part of 204 food-related FDA actions this month.
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 (Hy-Vee Stores Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Hy-Vee Stores Inc have FDA actions?
This is the only FDA action we have on record for Hy-Vee Stores Inc in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1304-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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