FDA Recall United States Completed 2026 recordClass II
House Of Flavors, Inc.
- Product
- 1972 Banana Pudding Ice Cream, 3 GAL, UPC 0 75196 00556 6
- Published
- January 21, 2026
- Distribution
- AL AZ CT GA IA IL IN KY MI MN MO NC NJ N…
House Of Flavors, Inc. Recall: Undeclared egg
United States
CompletedClass I
- Company
- House Of Flavors, Inc.
- Product
- House of Flavors 4893 Chicago Vanilla Naturally Flavored Ice…
- Recall date
- February 26, 2026
- Source
- FDA
Reason for recall
Undeclared egg
- - Recall initiated
- - Reported by source
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| House of Flavors 4893 Chicago Vanilla Naturally Flavored Ice Cream, 3 GAL tub | Not published in this source record | 4880 tubs | 24059, 24130, 24207, 24342, 25105, 25120, 25134, 25206, 25254, 25301 |
Distribution
- IL
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- H-0621-2026
- Event ID
- 98501
- Status
- Completed
- Classification
- Class I
- Company
- House Of Flavors, Inc.
- Product description
- House of Flavors 4893 Chicago Vanilla Naturally Flavored Ice Cream, 3 GAL tub
- Quantity
- 4880 tubs
- Reason
- Undeclared egg
- Recall initiation date
- February 26, 2026
- Report date
- March 18, 2026
- Classification date
- Not published in this source record
- Termination date
- Not terminated as of this source record
- Distribution pattern
- IL
- UPC, lot, and code information
- 24059, 24130, 24207, 24342, 25105, 25120, 25134, 25206, 25254, 25301
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: House Of Flavors, Inc.
Other recalls from House Of Flavors, Inc.
FDA Recall United States Completed 2026 recordClass II
House Of Flavors, Inc.
- Product
- 2248 Banana Pudding Ice Cream, 3 GAL, UPC 7 65265 81237 8
- Published
- January 21, 2026
- Distribution
- AL AZ CT GA IA IL IN KY MI MN MO NC NJ N…
FDA Recall United States Terminated Historical recordClass II
House Of Flavors, Inc.
- Product
- Giant Eagle churned Butter Pecan Reduced Fat 48FLOZ, UPC 030…
- Published
- December 18, 2024
- Distribution
- Retail stores in MD, OH, PA, and WV
A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| State | Distributed |
|---|---|
| Illinois | 1 |
States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class I mean?
A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.
Is this recall still active?
According to FDA, this recall's status is "Completed." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
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