Food Recall Check
Class I · High risk Terminated Initiated May 6, 2024 (2 years ago)

Hy-Vee To Go Cookies & Cream Mix recall

Recalled by Hy-Vee Stores Inc · West Des Moines, IA, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Potential Salmonella contamination

Pathogen: Salmonella

Salmonella is the most common cause of food recalls for bacteria, often in eggs, produce, nuts and spices.

The most serious food recalls: a contaminated product can cause outbreaks, hospitalisations and deaths, especially for pregnant people, young children, older adults and anyone with a weakened immune system. All bacteria & viruses recalls.

What was recalled

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.

Quantity: 154 cases (6 x 4oz containers); 619 cases (6 x 16oz containers)

Food: Milk & dairy Bread & bakery

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

Lot numbers 24073, 24101, and 24117

Where it was sold

Iowa Illinois Kansas Minnesota Missouri Nebraska South Dakota Wisconsin

FDA's distribution note: IA, IL, KS, MN, MO, NE, SD, WI

Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Hy-Vee Stores Inc
Initiated by
Voluntary: Firm initiated
Recall initiated
May 6, 2024
In FDA report of
Jun 5, 2024
Terminated
Jun 28, 2024
FDA recall number
F-1304-2024 · event 94579
Official record
FDA enforcement report search

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Reason An ingredient used as an ingredient in the products tested positive for Listeria monocytogenes

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