RecallRadar
High RiskReported March 18, 2026

House of Flavors 4893 Chicago Vanilla Naturally Flavored Ice Cream

Recalled by House Of Flavors, Inc.

Food recall

House Of Flavors, Inc.

Class I — most serious

There is a reasonable chance that using this product could cause serious health problems or death.

See all recalls involving an undeclared allergen

House Of Flavors, Inc. has recalled House of Flavors 4893 Chicago Vanilla Naturally Flavored Ice Cream, according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on March 18, 2026 and was initiated on February 26, 2026. It is classified as a Class I recall, which means there is a reasonable chance that using this product could cause serious health problems or death.

Below is a plain-English summary of what was recalled, why it was recalled, how to tell whether you have the affected product, and what steps you can take. For the complete and most current details, you can view the FDA record linked further down this page.

What was recalled?

This recall covers House of Flavors 4893 Chicago Vanilla Naturally Flavored Ice Cream, with approximately 4880 tubs affected. The company behind the recall is House Of Flavors, Inc., based in Ludington, MI. The FDA describes the product as: “House of Flavors 4893 Chicago Vanilla Naturally Flavored Ice Cream, 3 GAL tub”

Why was House of Flavors 4893 Chicago Vanilla Naturally Flavored Ice Cream recalled?

According to the FDA, the stated reason for the recall is: “Undeclared egg.” In plain terms, this recall relates to an undeclared ingredient or allergen.

An undeclared ingredient means a food contains something — often a major allergen such as milk, eggs, soy, wheat, peanuts, or tree nuts — that is not listed on the label. For most people this is not dangerous, but for someone with a food allergy or sensitivity it can trigger a serious reaction. Accurate labeling is required so that people can avoid ingredients they need to stay away from.

What should you do?

If you think you may have bought House of Flavors 4893 Chicago Vanilla Naturally Flavored Ice Cream, compare it against the product description and identifying codes (24059, 24130, 24207, 24342, 25105, 25120, 25134, 25206, 25254, 25301) before using it.

The general guidance for a matching product is to stop using it and follow the instructions in the official FDA recall notice, which may include a repair, replacement, refund, or safe disposal. When in doubt, contact House Of Flavors, Inc. or your local health authority.

About this recall

This recall was distributed in MI. RecallRadar summarizes recall information from public FDA data to make it easier to understand. We are an independent service and are not affiliated with the FDA or any government agency, so please always refer to the official source for the authoritative record — and note the “last synced” date shown on this page, since recall details can change over time.

Full recall details

Status
Completed
Date reported
March 18, 2026
Recall started
February 26, 2026
Distributed in
MI
What was recalled
House of Flavors 4893 Chicago Vanilla Naturally Flavored Ice Cream, 3 GAL tub
Why it was recalled (as stated by the FDA)
Undeclared egg
How to identify the affected product
24059, 24130, 24207, 24342, 25105, 25120, 25134, 25206, 25254, 25301
Amount recalled
4880 tubs

What you can do

Check whether any product you have matches the description and codes above. If it does, stop using it and follow the instructions in the official recall notice. When in doubt, contact the company or your local health authority.

Quick answers

Why was House of Flavors 4893 Chicago Vanilla Naturally Flavored Ice Cream recalled?+

According to the FDA: Undeclared egg

How serious is this recall?+

Class I — most serious. There is a reasonable chance that using this product could cause serious health problems or death.

What should I do if I have House of Flavors 4893 Chicago Vanilla Naturally Flavored Ice Cream?+

Compare your product against the description and identifying codes on this page. If it matches, stop using it and follow the instructions in the official recall notice — this usually means returning it for a refund or discarding it. When in doubt, contact the company or your local health authority.

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View the official FDA record

Opens the U.S. Food and Drug Administration (FDA) data for this recall.

Recall number: H-0621-2026. Information last synced from the FDA on July 6, 2026.

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