Class ICompletedVoluntary: Firm initiated
House Of Flavors, Inc.: food recall H-0621-2026
House Of Flavors, Inc. of Ludington, MI recalled House of Flavors 4893 Chicago Vanilla Naturally Flavored Ice Cream, 3 GAL tub. Reason: Undeclared egg. The FDA listed it as Class I in its Enforcement Report dated Mar 18, 2026; distribution: Illinois.
Record status as published: Completed. openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- Product
- House of Flavors 4893 Chicago Vanilla Naturally Flavored Ice Cream, 3 GAL tub
- Product quantity
- 4880 tubs
- Reason for recall
- Undeclared egg
- Codes, lots and dates on the package
- 24059, 24130, 24207, 24342, 25105, 25120, 25134, 25206, 25254, 25301
- Distribution pattern
- IL
- Recalling firm
- House Of Flavors, Inc., Ludington, MI
- Classification
- Class I — the FDA uses this class for a situation in which there is a reasonable probability that using or being exposed to the product will cause serious adverse health consequences or death.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Feb 26, 2026 |
| Classified by the FDA | Mar 24, 2026 |
| Published in the Enforcement Report | Mar 18, 2026 |
Other recalls by House Of Flavors, Inc.
- H-0384-2026 · Jan 21, 2026 · Class II — Undeclared soy lecithin
- H-0383-2026 · Jan 21, 2026 · Class II — Undeclared soy lecithin
- F-0266-2025 · Dec 18, 2024 · Class II — Undeclared soy (soy lecithin).
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-0621-2026 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
- Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service. The FDA does not endorse OpenPlate.