RecallRadar
ModerateReported January 21, 2026

2248 Banana Pudding Ice Cream, 3 GAL, UPC 7 65265 81237 8

Recalled by House Of Flavors, Inc.

Food recall

House Of Flavors, Inc.

Class II — moderate

Using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.

See all recalls involving an undeclared allergen

House Of Flavors, Inc. has recalled 2248 Banana Pudding Ice Cream, 3 GAL, UPC 7 65265 81237 8, according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on January 21, 2026 and was initiated on December 12, 2025. It is classified as a Class II recall, which means using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.

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 2248 Banana Pudding Ice Cream, 3 GAL, UPC 7 65265 81237 8, with approximately 34,561 units affected. The company behind the recall is House Of Flavors, Inc., based in Ludington, MI. The FDA describes the product as: “2248 Banana Pudding Ice Cream, 3 GAL, UPC 7 65265 81237 8”

Why was 2248 Banana Pudding Ice Cream, 3 GAL, UPC 7 65265 81237 8 recalled?

According to the FDA, the stated reason for the recall is: “Undeclared soy lecithin.” 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 2248 Banana Pudding Ice Cream, 3 GAL, UPC 7 65265 81237 8, compare it against the product description and identifying codes (Lot numbers: 23222, 23283, 24019, 24051, 24248, 25070, 25247) 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
January 21, 2026
Recall started
December 12, 2025
Distributed in
MI
What was recalled
2248 Banana Pudding Ice Cream, 3 GAL, UPC 7 65265 81237 8
Why it was recalled (as stated by the FDA)
Undeclared soy lecithin
How to identify the affected product
Lot numbers: 23222, 23283, 24019, 24051, 24248, 25070, 25247
Amount recalled
34,561 units

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 2248 Banana Pudding Ice Cream, 3 GAL, UPC 7 65265 81237 8 recalled?+

According to the FDA: Undeclared soy lecithin

How serious is this recall?+

Class II — moderate. Using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.

What should I do if I have 2248 Banana Pudding Ice Cream, 3 GAL, UPC 7 65265 81237 8?+

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-0383-2026. Information last synced from the FDA on July 6, 2026.

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