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House Of Flavors, Inc. Recall: Undeclared soy (soy lecithin).

United States

TerminatedClass II

Company
House Of Flavors, Inc.
Product
Giant Eagle churned Butter Pecan Reduced Fat 48FLOZ, UPC 030…
Recall date
November 11, 2024
Terminated
January 30, 2025
Source
FDA

Reason for recall

Undeclared soy (soy lecithin).

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Giant Eagle churned Butter Pecan Reduced Fat 48FLOZ, UPC 030034940430; 6 retail units per case 030034940430 59 cases BEST BY MARCH 10, 2026

Distribution

  • Retail stores in MD
  • OH
  • PA
  • and WV

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0266-2025
Event ID
95761
Status
Terminated
Classification
Class II
Company
House Of Flavors, Inc.
Product description
Giant Eagle churned Butter Pecan Reduced Fat 48FLOZ, UPC 030034940430; 6 retail units per case
Quantity
59 cases
Reason
Undeclared soy (soy lecithin).
Recall initiation date
November 11, 2024
Report date
December 18, 2024
Classification date
Not published in this source record
Termination date
January 30, 2025
Distribution pattern
Retail stores in MD, OH, PA, and WV
UPC, lot, and code information
UPC 030034940430; BEST BY MARCH 10, 2026
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
E-Mail
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.

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FDA Recall United States Completed 2026 recordClass II

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Product
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Published
January 21, 2026
Distribution
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Product
2248 Banana Pudding Ice Cream, 3 GAL, UPC 7 65265 81237 8
Published
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Distribution
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Distribution map

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.

Distribution map
State Distributed
Maryland 1
Ohio 1
Pennsylvania 1
West Virginia 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 II mean?

A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.

Is this recall still active?

According to FDA, this recall's status is "Terminated." 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.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.