FDA Recall United States Terminated Historical recordClass II
Great Lakes Coca-Cola Distribution LLC
- Product
- Coco-Cola Original Taste, 12 Fl Oz. (355mL). Can UPC 0 4900…
- Published
- April 2, 2025
- Distribution
- IL and WI
Great Lakes Coca-Cola Distribution LLC Recall: Immediate package labeled as zero sugar contains the full sugar variety
United States
TerminatedClass II
- Company
- Great Lakes Coca-Cola Distribution LLC
- Product
- Fanta Orange 12pk (12, 12 oz. cans) Wrap UPC 0 4900003073 0
- Recall date
- June 1, 2023
- Terminated
- February 13, 2024
- Source
- FDA
Reason for recall
Immediate package labeled as zero sugar contains the full sugar variety
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Fanta Orange 12pk (12, 12 oz. cans) Wrap UPC 0 4900003073 0 | Not published in this source record | 14074 cases | Date Code: FEB1224DDB1956 |
Distribution
- California
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-1009-2023
- Event ID
- 92492
- Status
- Terminated
- Classification
- Class II
- Company
- Great Lakes Coca-Cola Distribution LLC
- Product description
- Fanta Orange 12pk (12, 12 oz. cans) Wrap UPC 0 4900003073 0
- Quantity
- 14074 cases
- Reason
- Immediate package labeled as zero sugar contains the full sugar variety
- Recall initiation date
- June 1, 2023
- Report date
- July 5, 2023
- Classification date
- Not published in this source record
- Termination date
- February 13, 2024
- Distribution pattern
- California
- UPC, lot, and code information
- Date Code: FEB1224DDB1956
- 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
Responsible company: Great Lakes Coca-Cola Distribution LLC
Other recalls from Great Lakes Coca-Cola Distribution LLC
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 "Terminated." 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.
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