Recall record at a glance
| Official record | F-1287-2019 |
|---|---|
| Category | Food Recalls |
| Classification | Class III |
| FDA record status | Terminated |
| Recalling firm | Pepsico Inc. |
| Report date | Apr 24, 2019 |
| Recall initiation date | Apr 5, 2019 |
| Quantity | 9,214 cases |
| Location | Purchase, NY, United States |
Official product description
Diet Pepsi, Classic Diet Pepsi Taste; 12 fl. oz. cans; Sold in 6,12, 20, 24 and 36-packs 12-Pack UPC: 0 12000 17186 4: 20-Pack UPC: 0 12000 17184 0: 24-Pack Cube UPC: 0 12000 17185 7: 24-Pack Slab UPC: 0 12000 17178 9: 36-Pack UPC: 1 12000 17180 2
Why the product was recalled
The outer case indicates that the product contains Aspartame; however, the wrap on the individual cans state that the product is Aspartame free.
Distribution information
Southern CA. Distribution list is forthcoming.
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.