RecallHawk
Class I Recall

House of Flavors 4893 Chicago Vanilla Naturally Flavored Ice Cream, 3 GAL tub

House Of Flavors, Inc.

Summary

The FDA issued a Class I for House of Flavors 4893 Chicago Vanilla Naturally Flavored Ice Cream, 3 GAL tub by House Of Flavors, Inc.. Reason: Undeclared egg.

Details

Source

Food Recall

External ID

H-0621-2026

Action Date

2026-03-18

Status

Completed

Category

food

Product Description

House of Flavors 4893 Chicago Vanilla Naturally Flavored Ice Cream, 3 GAL tub

Lot/Code Info: 24059, 24130, 24207, 24342, 25105, 25120, 25134, 25206, 25254, 25301

Quantity Affected: 4880 tubs

Reason for Recall

Undeclared egg

Distribution

IL

Type: Voluntary: Firm initiated

Recall Initiated: 2026-02-26

Company

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 35 food recalls issued in the same week, part of 204 food-related FDA actions this month.

House Of Flavors, Inc. has 4 FDA actions in our database, including 4 recalls.

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 (House Of Flavors, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does House Of Flavors, Inc. have FDA actions?

House Of Flavors, Inc. has 4 FDA actions in our database, including 4 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-0621-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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