“Publix Rich & Creamy Vanilla Ice Cream Recall: Undeclared Eggs Hazard.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/7074-publix-rich-creamy-vanilla-ice-cream-recall-undeclared-eggs-hazard. Based on FDA recall #H-0192-2026.
Publix Super Markets, Inc. recalled Publix Rich & Creamy Vanilla Ice Cream due to undeclared eggs, the FDA said on Oct. 14, 2025. The voluntary Class I recall affects 1,452 units distributed in Florida, Georgia, Alabama and Kentucky.
How to tell if you have it
Brand: Publix
Product: Publix Rich & Creamy Vanilla Ice Cream
Date Code: Jun19, 2026 A
Lote Code: PLT 13-575
Item Code: 64375
Distribution: FL, GA, AL, KY
The hazard
The product contains undeclared eggs, which can cause allergic reactions in individuals with egg allergies. The FDA classified the recall as Class I.
Context
GovInfoNow's records show Publix Super Markets, Inc. has 15 other recalls on record since Sept. 5, 2014. Recent Publix recalls include a June 25, 2026 recall of Organic Mixed Berries for E. coli O145:H28 contamination risk and a May 9, 2025 recall of Greenwise Baby Food Pouches for elevated levels of lead, cadmium and arsenic. Other recent recalls of similar products include House of Flavors Vanilla Ice Cream (Feb. 26, 2026) and Loard's Egg Nog Ice Cream (April 15, 2026).
How to tell if you have this one
Check for the Date Code: Jun19, 2026 and Lote Code: PLT 13-575 on the ice cream packaging. The product is sold under Publix brand.
Brand
Publix
Category
Food
Based on the official FDA remedy
What to do — step by step
Check Product Label
Look for the Date Code: Jun19, 2026 and Lote Code: PLT 13-575 on the ice cream packaging.
Where it went and when
Where it was distributed
Distributed in 4 states.
Listed by the agency
Not listed
FDA distribution: “FL, GA, AL, KY” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Alabama, Florida, Georgia, Kentucky.
Recall timeline
FDA terminated this recall 38 days after the firm started it.
1Firm started the recall
2FDA classified it Class I
3FDA terminated the recall
4Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #H-0192-2026 (October 14, 2025)
Plain-language summary written by qwen3:4b on August 17, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.