FDA Recall United States Ongoing Historical recordClass II
G.O. Corporation
- Product
- Lett. Salad Shred Mix w/Rom, Produce Code 458009, 4-5 lb. b…
- Published
- August 23, 2023
- Distribution
- Multiple states
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Policy version 2026-07-21, effective July 21, 2026.
United States
OngoingClass II
Romaine lettuce may be contaminated with deer feces.
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Romaine lettuce packaged into the following configurations and sizes: 1. Lettuce Romaine Shred, Produce Code 720325, 4-2.5lb. bags per shipping case, Customer UPC 9120457. 2. Romaine Shred 1/4", Produce Code 720425, 4-2.5lb bags per shipping case, Customer UPC 7641269 and 8095202. 3. Lettuce Romaine Shred, Produce Code 720449, 8-2.5lb.bags per shipping case, Customer UPC 7166295 and 7599586. 4. 1.5XRandom, Produce Code 720625, 4-2.5lb bags per shipping case Customer UPC 1672815. 5. 1.5XRandom, Produce Code 720725, 4-2.5lb bags per shipping case, Customer UPC 1855196 and 8950701. 6. 1.5XRandom, Produce Code 720732, 6-2lb bags per shipping case, Customer UPC 3179397 and 4106811. 7. 1.5XRandom, Produce Code 720747, 3-2lb bags per shipping case, Customer UPC 3100922. 8. Medium, Produce Code 720832, 6-2lb per shipping case, Customer UPC 5087588. 9. Medium, Produce Code 720840, 10-2lb per shipping case, Customer UPC 720840. | 9120457 | 23,186 lbs. total | Lot Codes: 1. 130208, 130209, 130212; 2. 130208, 130209, 130212; 3. 130209; 4. 130209, 130212; 5. 130209, 130212; 6. 130209, 130212; 7. 130209, 130212; 8. 130209, 130212; 9. 130212. |
This recall shares FDA event ID 92828 with 7 other product entries in Public Health Trace.
FDA Recall United States Ongoing Historical recordClass II
FDA Recall United States Ongoing Historical recordClass II
FDA Recall United States Ongoing Historical recordClass II
FDA Recall United States Ongoing Historical recordClass II
FDA Recall United States Ongoing Historical recordClass II
FDA Recall United States Ongoing Historical recordClass II
FDA Recall United States Ongoing Historical recordClass II
Responsible company: G.O. Corporation
FDA Recall United States Ongoing Historical recordClass II
FDA Recall United States Ongoing Historical recordClass II
FDA Recall United States Ongoing Historical recordClass II
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.
| State | Distributed |
|---|---|
| Iowa | 1 |
| Minnesota | 1 |
| North Dakota | 1 |
| Wisconsin | 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.
View FDA enforcement record -- the specific openFDA record this summary was built from.
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View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.
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