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Publix Super Markets, Inc. Recall: Undeclared Eggs

United States

TerminatedClass I

Company
Publix Super Markets, Inc.
Product
Publix Rich & Creamy Vanilla Ice Cream
Recall date
October 14, 2025
Terminated
November 21, 2025
Source
FDA

Reason for recall

Undeclared Eggs

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Publix Rich & Creamy Vanilla Ice Cream Not published in this source record 1,452 units Date Code:Jun19, 2026 A Lote Code: PLT 13-575 Item Code: 64375

Distribution

  • FL
  • GA
  • AL
  • KY

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
H-0192-2026
Event ID
97837
Status
Terminated
Classification
Class I
Company
Publix Super Markets, Inc.
Product description
Publix Rich & Creamy Vanilla Ice Cream
Quantity
1,452 units
Reason
Undeclared Eggs
Recall initiation date
October 14, 2025
Report date
November 26, 2025
Classification date
Not published in this source record
Termination date
November 21, 2025
Distribution pattern
FL, GA, AL, KY
UPC, lot, and code information
Date Code:Jun19, 2026 A Lote Code: PLT 13-575 Item Code: 64375
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: Publix Super Markets, Inc.

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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
Florida 1
Georgia 1
Alabama 1
Kentucky 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 "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.

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