Recall record at a glance
| Official record | F-0772-2024 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | CF Dallas LLC |
| Report date | Jan 24, 2024 |
| Recall initiation date | Nov 20, 2023 |
| Quantity | 27,998 units |
| Location | Grand Prairie, TX, United States |
Official product description
Seasonal Blend 10oz, Seasonal Blend 16oz, Seasonal Blend 42oz , Melon Trio 16oz, Melon Mix 32oz, Fruit Blend 16oz, Fruit Bowl 40oz, Seasonal Fruit Tray 48oz, Fruit Mix 32oz, Cantaloupe Chunks 10oz, Cantaloupe Chunks 16oz, Fruit Medley 6oz- all packaged in clear plastic clamshells/ cups
Why the product was recalled
The select fresh-cut products were made from whole cantaloupe subject to a previously announced voluntary recall initiated by Sofia Produce, LLC dba Trufresh. The whole cantaloupe may have the potential to be contaminated with Salmonella.
Distribution information
Select retail stores in Indiana, Michigan, Ohio, Kentucky, North Carolina, Tennessee, Virginia, Illinois, Texas, and Louisiana
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.