Lower riskFood recall · FDA · Published May 6, 2024
Hy-Vee To Go Cookies & Cream Mix Recall: Potential Salmonella Contamination
Hy-Vee recalls 4oz and 16oz Cookies & Cream Mix due to potential Salmonella contamination. Affected lots include 24073, 24101, and 24117. Consumers should check UPCs and lot numbers for affected products.
“Hy-Vee To Go Cookies & Cream Mix Recall: Potential Salmonella Contamination.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/9313-hy-vee-to-go-cookies-cream-mix-recall-potential-salmonella. Based on FDA recall #F-1304-2024 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1304-2024%22&limit=1).
The FDA announced on May 6, 2024, that Hy-Vee Stores Inc. is recalling Hy-Vee To Go Cookies & Cream Mix due to potential Salmonella contamination. The recall affects products distributed in Iowa, Illinois, Kansas, Minnesota, Missouri, Nebraska, South Dakota, and Wisconsin.
How to tell if you have it
Brand: Hy-Vee
Product: Hy-Vee To Go Cookies & Cream Mix, Net wt. 4 oz (113g), UPC 0075450486740
Product: Hy-Vee Cookies & Cream Mix, Net Wt. 16oz (453g), UPC 0075450486730
Lot numbers: 24073, 24101, and 24117
The hazard
The products pose a potential Salmonella contamination hazard. The FDA classified this as a Class I recall.
Context
GovInfoNow's records show Hy-Vee Stores Inc has issued five other recalls since March 3, 2016, including a May 24, 2021, undeclared egg allergen hazard and a Nov. 24, 2020, Listeria risk. Other recent recalls of similar products include the Doughy Chocolate Chip Cookie Dough Recall (Nov. 20, 2025), the Griffith Foods Milk-Egg Mix Recall (March 11, 2026), and the Ghirardelli Vanilla Frappe Mix Recall (April 26, 2026).
How to tell if you have this one
Check for the UPC 0075450486740 (4oz) or 0075450486730 (16oz) on the product packaging. The affected lot numbers are 24073, 24101, and 24117.
Brand
Hy-Vee
Category
Food
Based on the official FDA remedy
What to do — step by step
Check Product UPC
Look for the UPC 0075450486740 (4oz) or 0075450486730 (16oz) on the product packaging.
Identify Affected Lot Numbers
The affected lot numbers are 24073, 24101, and 24117.
Where it went and when
Where it was distributed
Distributed in 8 states.
Listed by the agency
Not listed
FDA distribution: “IA, IL, KS, MN, MO, NE, SD, WI” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Illinois, Iowa, Kansas, Minnesota, Missouri, Nebraska, South Dakota, Wisconsin.
Recall timeline
FDA terminated this recall 53 days after the firm started it.
1Firm started the recall
2Published in FDA’s Enforcement Report
3FDA classified it Class I
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #F-1304-2024 (May 6, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1304-2024 to see it in context.
Plain-language summary written by qwen3:4b on August 17, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.