RecallRadar
High RiskReported November 26, 2025

Publix Rich & Creamy Vanilla Ice Cream

Recalled by Publix Super Markets, Inc.

Food recall

Publix Super Markets, Inc.

Class I — most serious

There is a reasonable chance that using this product could cause serious health problems or death.

See all recalls involving an undeclared allergen

Publix Super Markets, Inc. has recalled Publix Rich & Creamy Vanilla Ice Cream, according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on November 26, 2025 and was initiated on October 14, 2025. It is classified as a Class I recall, which means there is a reasonable chance that using this product could cause serious health problems or death.

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 Publix Rich & Creamy Vanilla Ice Cream, with approximately 1,452 units affected. The company behind the recall is Publix Super Markets, Inc., based in Lakeland, FL. The FDA describes the product as: “Publix Rich & Creamy Vanilla Ice Cream”

Why was Publix Rich & Creamy Vanilla Ice Cream recalled?

According to the FDA, the stated reason for the recall is: “Undeclared Eggs.” 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 Publix Rich & Creamy Vanilla Ice Cream, compare it against the product description and identifying codes (Date Code:Jun19, 2026 A Lote Code: PLT 13-575 Item Code: 64375) 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 Publix Super Markets, Inc. or your local health authority.

About this recall

This recall was distributed in FL. 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
Terminated
Date reported
November 26, 2025
Recall started
October 14, 2025
Distributed in
FL
What was recalled
Publix Rich & Creamy Vanilla Ice Cream
Why it was recalled (as stated by the FDA)
Undeclared Eggs
How to identify the affected product
Date Code:Jun19, 2026 A Lote Code: PLT 13-575 Item Code: 64375
Amount recalled
1,452 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 Publix Rich & Creamy Vanilla Ice Cream recalled?+

According to the FDA: Undeclared Eggs

How serious is this recall?+

Class I — most serious. There is a reasonable chance that using this product could cause serious health problems or death.

What should I do if I have Publix Rich & Creamy Vanilla Ice Cream?+

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-0192-2026. Information last synced from the FDA on July 6, 2026.