Recall record at a glance
| Official record | F-1906-2018 |
|---|---|
| Category | Food Recalls |
| Classification | Class II |
| FDA record status | Terminated |
| Recalling firm | The Coca-Cola Company |
| Report date | Sep 5, 2018 |
| Recall initiation date | Aug 3, 2018 |
| Quantity | 432 bottles (18 cases packed 24/12 fluid oz. bottles) |
| Location | Atlanta, GA, United States |
Official product description
Consumer Packaging (PET bottle): Minute Maid TROPICAL BLEND Flavored Juice Beverage 12 FL OZ (355mL), JAN0719NPA, UPC: 0 25000 06229 2. Master Case: packaged 24/12 fl.oz., GTIN number 00025000062414 (no UPC)
Why the product was recalled
Foreign matter believed to be glass observed in retain samples of product.
Distribution information
Retail product distributed to VA. Identity of distributor(s) of the 432 bottles was not provided and is not available at this time. RES currently shows 1 distributor and will be updated with any new information that is received. Update (08/24/18): Product was distributed to 4 distributors - 2 of these distributors distributed the 432 bottles (18 cases); see uploaded e-mails beginning with "8-22-18" and "8-24-18".
How to read the classification
FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.
Additional record details
Recall type: Voluntary: Firm initiated. Initial notification: Telephone.
What to do next
If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.
About this record
Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.
FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.