Recall record at a glance
| Official record | F-0578-2024 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | Vinyard Fruit & Vegetable Co., LLC |
| Report date | Dec 20, 2023 |
| Recall initiation date | Nov 10, 2023 |
| Quantity | 599 cases and 459 each |
| Location | Oklahoma City, OK, United States |
Official product description
Fruit Medley Cup 16/6 oz 3300-3 Cantaloupe Cube (2/5 lb) 3338-3 Fruit Mix Kit (4/5 lb) (Tray) 2963-3 3 Melon 16/6 oz cups 3330-3 Fruit Mix (2/5 lb) 3301-3 Cantaloupe Cube (5 lb) 3304-3 Cantaloupe Cubed 10/12 oz cups 0526-3 Melon Variety Pack 2964-3 3 Melon Medley 6 oz cups 2973-3 Fruit Medley 6 oz cups 2976-3 Cantaloupe Chunks 6 oz cups
Why the product was recalled
The affected product is being recalled from the marketplace due to possible Salmonella contamination.
Distribution information
Product was all distributed within the state of Oklahoma. Product was distributed to food services, distributions centers and to 7-11 convenience stores.
How to read the classification
FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.
Additional record details
Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.
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.