Class IITerminatedVoluntary: Firm initiated
Great Lakes Coca-Cola Distribution LLC: food recall F-0664-2025
Great Lakes Coca-Cola Distribution LLC of Niles, IL recalled Coco-Cola Original Taste, 12 Fl Oz. (355mL). Can UPC 0 49000-00634 6. 12-can pack UPC 0 49000-02890 4. Canned Under… Reason: Foreign object (plastic). The FDA listed it as Class II in its Enforcement Report dated Apr 2, 2025; distribution: Illinois, Wisconsin.
Record status as published: Terminated (terminated May 28, 2025). openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- Product
- Coco-Cola Original Taste, 12 Fl Oz. (355mL). Can UPC 0 49000-00634 6. 12-can pack UPC 0 49000-02890 4. Canned Under Authority of the Coca-Cola Company, Atlanta, GA 30313.
- Product quantity
- 864 - 12 count packs
- Reason for recall
- Foreign object (plastic)
- Codes, lots and dates on the package
- Date Code: SEP2925MDA Time Stamp: 1100-1253
- Distribution pattern
- IL, WI
- Recalling firm
- Great Lakes Coca-Cola Distribution LLC, Niles, IL
- Classification
- Class II — the FDA uses this class for a situation in which using or being exposed to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Mar 6, 2025 |
| Classified by the FDA | Mar 24, 2025 |
| Published in the Enforcement Report | Apr 2, 2025 |
| Terminated | May 28, 2025 |
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number F-0664-2025 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
- Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service. The FDA does not endorse OpenPlate.