Romaine lettuce packaged into the following configurations and sizes: 1. Lettuce Romaine Shred, Produce Code 720325
Summary
The FDA issued a Class II for Romaine lettuce packaged into the following configurations and sizes: 1. Le by G.O. Corporation. Reason: Romaine lettuce may be contaminated with deer feces..
Details
Source
Food Recall
External ID
F-1423-2023
Action Date
2023-08-23
Status
Ongoing
Category
food
Product Description
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.
Lot/Code Info: 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.
Quantity Affected: 23,186 lbs. total
Reason for Recall
Romaine lettuce may be contaminated with deer feces.
Distribution
IA, MN, ND, WI
Type: Voluntary: Firm initiated
Recall Initiated: 2023-08-01
Company
Minneapolis, MN
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 85 food recalls issued in the same week, part of 204 food-related FDA actions this month.
G.O. Corporation has 11 FDA actions in our database, including 11 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (G.O. Corporation) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does G.O. Corporation have FDA actions?
G.O. Corporation has 11 FDA actions in our database, including 11 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1423-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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