Food Recall Check
Class I · High risk Terminated Initiated Aug 26, 2025 (14 months ago)

o Nagatoshi Large AA Brown Omega-3 1 dozen cartons o Nijiya Large… recall

Recalled by Country Eggs, LLC · Lucerne Valley, CA, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Shell egg product potentially contaminated with salmonella.

Pathogen: Salmonella

Salmonella is the most common cause of food recalls for bacteria, often in eggs, produce, nuts and spices.

The most serious food recalls: a contaminated product can cause outbreaks, hospitalisations and deaths, especially for pregnant people, young children, older adults and anyone with a weakened immune system. All bacteria & viruses recalls.

What was recalled

o Nagatoshi Large AA Brown Omega-3 1 dozen cartons o Nijiya Large AA Brown Golden Yolk 1 dozen cartons o Mizuho Large AA Brown Omega-3 Cage 1 dozen cartons o Country Eggs Large AA Brown Sunshine Yolk 15 dozen bulk loose

Quantity: 81,542 dozen across all brands

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

Sell By dates of 07/01/2025- 09/18/2025

Where it was sold

California Nevada

FDA's distribution note: Product was distributed to 11 consignees across California and Nevada. No foreign or institution distribution.

Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Country Eggs, LLC
Initiated by
Voluntary: Firm initiated
Recall initiated
Aug 26, 2025
In FDA report of
Oct 15, 2025
Terminated
Feb 26, 2026
FDA recall number
H-0011-2026 · event 97512
Official record
FDA enforcement report search