CLASS I Food recall · Reported 26 Apr 2023 · FDA Enforcement Report

HyVee Hamburger Chili Macaroni Skillet Meal retail recalled

Gilster-Mary Lee is recalling HyVee Hamburger Chili Macaroni Skillet Meal retail, distributed in 8 states. The recall was initiated on 23 Mar 2023 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesBest By FEB 08 24 Y18

Quantity recalled4452 retail units

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number: F-0739-2023
FDA event ID: 91971
Recalling firm: Gilster-Mary Lee, Chester, IL
Brand: HyVee Hamburger
Classification: Class I
Status: Terminated
Recall initiated: 23 Mar 2023
FDA classified: 18 Apr 2023
Reported: 26 Apr 2023
Type: Voluntary: Firm initiated
Customers notified by: E-Mail
Reason category: Undeclared Milk
Product category: Herbal Supplements

Timeline

23 Mar 2023	Recall initiated by company
18 Apr 2023	Classified by FDA	+26 days
26 Apr 2023	Published in enforcement report	+8 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Undeclared milk

Product as listed by the FDA

HyVee Hamburger Chili Macaroni Skillet Meal, 5.2oz retail carton. UPC: 0 75450-08552 5

Where it was distributed

HyVee Retail Stores in Iowa, Illinois, Missouri, Kansas, Nebraska, South Dakota, Minnesota and Wisconsin

Iowa Illinois Kansas Minnesota Missouri Nebraska South Dakota Wisconsin

Stores named: Hy-Vee

Questions about this recall

Why was it recalled?

Undeclared milk

Which lots are affected?

Best By FEB 08 24 Y18

Where was it sold?

HyVee Retail Stores in Iowa, Illinois, Missouri, Kansas, Nebraska, South Dakota, Minnesota and Wisconsin

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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