Romaine Lettuce (G.O. Corporation) – Deer Feces Contamination (2023)
Class II: A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Class II recall indicates potential for temporary health effects.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
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.
Brand
G.O. Corporation
Lot Codes / Batch Numbers
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.
Products Sold
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.
G.O. Corporation is recalling Romaine lettuce packaged into the following configurations and sizes: 1. Lettuce Romaine Shred, due to Romaine lettuce may be contaminated with deer feces.. This is a Class I recall, indicating a high risk of serious health consequences. Based on FDA enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Romaine lettuce may be contaminated with deer feces.
Recommended Action
Per FDA guidance
Consumers should stop using the product and contact the recalling firm or return it to the place of purchase.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
IA, MN, ND, WI
Page updated: Jan 6, 2026