Recall record at a glance
| Official record | H-0210-2025 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Ongoing |
| Recalling firm | August Egg Company |
| Report date | Jul 9, 2025 |
| Recall initiation date | Jun 6, 2025 |
| Quantity | 20,400,000 eggs (1,700,000 dozen) |
| Location | Hilmar, CA, United States |
Official product description
--- Shell Eggs; Brown; Various sizes - medium, large, and jumbo; Various pack sizes - 5, 12, 18, and Loose ---- Clover Organic Large Brown 12 eggs --- First Street Cage Free Large Brown Loose (1 case = 150 eggs) --- Nulaid Medium Brown Cage Free 12 eggs --- Nulaid Jumbo Brown Cage Free 12 eggs --- O Organics Cage Free Large Brown 6 eggs --- O Organics Large Brown 12 eggs --- O Organics Large Brown 18 eggs --- Marketside Organic Large Cage Free Brown 12 eggs --- Marketside Organic Large Cage Free Brown 18 eggs --- Marketside Large Cage Free Brown 12 eggs --- Marketside Large Cage Free Brown 18 eggs --- Raley's Large Cage Free Brown 12 eggs --- Raley's Large Cage Free Brown 18 eggs --- Raley's Organic Large Cage Free Brown 12 eggs --- Raley's Organic Large Cage Free Brown 18 eggs --- Simple Truth Medium Brown Cage Free 18 eggs --- Simple Truth Large Brown Cage Free 18 eggs --- Sun Harvest Organic Cage Free Large Brown 12 eggs --- Sun Harvest Organic Cage Free Large Brown 18 eggs --- Sunnyside Large Brown Cage Free 12 eggs --- Sunnyside Large Brown Cage Free 18 eggs --- Sunnyside Organic Cage Free Large Brown 12 eggs --- Sunnyside Organic Cage Free Large Brown 18 eggs --- Loose Small Brown Cage Free (1 box = 6 flats; 1 flat= 30 eggs) --- Loose Medium Brown Cage Free (1 box = 6 flats; 1 flat= 30 eggs) --- Loose Medium Brown Organic (1 box = 6 flats; 1 flat= 30 eggs) --- Loose Large Brown Organic (1 box = 6 flats; 1 flat = 30 eggs) --- Loose Jumbo Brown Cage Free (1 box = 5 flats; 1 flat = 20 eggs) --- Loose Jumbo Brown Organic (1 box = 5 flats; 1 flat = 20 eggs)
Why the product was recalled
Potential contamination with Salmonella.
Distribution information
AZ, CA, IL, IN, NE, NM, NV, WA, WY
How to read the classification
FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.
Additional record details
Recall type: Voluntary: Firm initiated. Initial notification: Press Release.
What to do next
If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.
About this record
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