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
G.O. Corporation Recall: Romaine lettuce may be contaminated with deer feces.
United States
OngoingClass II
- Company
- G.O. Corporation
- Product
- Lettuce Mix w 20 Romaine, Produce Code 421009, 4-5 lb. bags…
- Recall date
- August 1, 2023
- Source
- FDA
Reason for recall
Romaine lettuce may be contaminated with deer feces.
- - Recall initiated
- - Reported by source
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Lettuce Mix w 20 Romaine, Produce Code 421009, 4-5 lb. bags per shipping case, | Not published in this source record | 23,186 lbs. total | Lot Code: 130212 |
Distribution
- IA
- MN
- ND
- WI
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-1426-2023
- Event ID
- 92828
- Status
- Ongoing
- Classification
- Class II
- Company
- G.O. Corporation
- Product description
- Lettuce Mix w 20 Romaine, Produce Code 421009, 4-5 lb. bags per shipping case,
- Quantity
- 23,186 lbs. total
- Reason
- Romaine lettuce may be contaminated with deer feces.
- Recall initiation date
- August 1, 2023
- Report date
- August 23, 2023
- Classification date
- Not published in this source record
- Termination date
- Not terminated as of this source record
- Distribution pattern
- IA, MN, ND, WI
- UPC, lot, and code information
- Lot Code: 130212
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Letter
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Other products recalled under this same event
This recall shares FDA event ID 92828 with 7 other product entries in Public Health Trace.
FDA Recall United States Ongoing Historical recordClass II
G.O. Corporation
- Product
- Lettuce Romaine All American, packaged in the following size…
- Published
- August 23, 2023
- Distribution
- Multiple states
FDA Recall United States Ongoing Historical recordClass II
G.O. Corporation
- Product
- Lettuce Rom Blend 50/50, packaged in the following sizes and…
- Published
- August 23, 2023
- Distribution
- Multiple states
FDA Recall United States Ongoing Historical recordClass II
G.O. Corporation
- Product
- Lett. Blend Rom/End/Rad-All Seasons packaged in the followin…
- Published
- August 23, 2023
- Distribution
- Multiple states
FDA Recall United States Ongoing Historical recordClass II
G.O. Corporation
- Product
- Lettuce Salad Blend Monterey, Produce Code 404709, 4-5lb. ba…
- Published
- August 23, 2023
- Distribution
- Multiple states
FDA Recall United States Ongoing Historical recordClass II
G.O. Corporation
- Product
- Romaine lettuce packaged into the following configurations a…
- Published
- August 23, 2023
- Distribution
- Multiple states
FDA Recall United States Ongoing Historical recordClass II
G.O. Corporation
- Product
- Lettuce Romaine 80/20 GB, packaged in the following sizes an…
- Published
- August 23, 2023
- Distribution
- Multiple states
Responsible company: G.O. Corporation
Other recalls from G.O. Corporation
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
FDA Recall United States Ongoing Historical recordClass II
G.O. Corporation
- Product
- Lettuce Romaine All American, packaged in the following size…
- Published
- August 23, 2023
- Distribution
- Multiple states
FDA Recall United States Ongoing Historical recordClass II
G.O. Corporation
- Product
- Lettuce Rom Blend 50/50, packaged in the following sizes and…
- Published
- August 23, 2023
- Distribution
- Multiple states
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.
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class II mean?
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.
Is this recall still active?
According to FDA, this recall's status is "Ongoing." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.
