Recall record at a glance
| Official record | F-2848-2015 |
|---|---|
| Category | Food Recalls |
| Classification | Class III |
| FDA record status | Terminated |
| Recalling firm | Dr. Pepper Snapple Group Inc. |
| Report date | Jul 22, 2015 |
| Recall initiation date | Jun 10, 2015 |
| Quantity | 4,158 cs/24/20 oz bottles |
| Location | Plano, TX, United States |
Official product description
Diet Bubba Cola, 20 FL. OZ (1.25 PT) 591 mL INGREDIENTS: CARBONATED WATER, HIGH FRUCTOSE CORN SYRUP, CARAMEL COLOR, PHOSPHORIC ACID, NATURAL FLAVOR, CAFFEINE. DISTRIBUTED BY: SAVE-A-LOT FOOD STORES, LTD. EARTH CITY, MO 63045 0 51933 34484 6
Why the product was recalled
The firm was notified by one of it's retail stores that the ingredient statement does not declare citric acid, potassium benzoate, aspartame, and acesulfame potassium. The product contains the label for a regular drink instead of a diet drink.
Distribution information
Product was shipped to the following states: CA, CO, FL, GA, IL, IN, KY, LA, MD, MI, MO, NY, OH, TN, TX & WI.
How to read the classification
FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.
Additional record details
Recall type: Voluntary: Firm initiated. Initial notification: Letter.
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.