Recall record at a glance
| Official record | F-0583-2024 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | Cut Fruit Express, Inc. |
| Report date | Dec 20, 2023 |
| Recall initiation date | Nov 24, 2023 |
| Quantity | 123 units |
| Location | Inver Grove Heights, MN, United States |
Official product description
Mixed Fruit Products that contain Cantaloupe, Honeydew, Pineapple, and Red Grapes Identified with the following Item ID and Description. 1. 11658 Fruit Mix, CHPG 5lb. (GR#11658) 2. 4703 Fruit Spear CHWP 15oz 3. 4768 Fruit Mix CHPG 6.5oz Lacer 4. 4774 Fruit Mix, CrGHP 6-6.5oz Lacer 5. 4852 Fruit Tray Round 2.5lb. 6. 9038716 Fruit Mix CrgHP 24-6oz Lacert 7. ET612 Fruit Mix CHPG 6/16 oz.
Why the product was recalled
Cantaloupe containing products may be contaminated with Salmonella.
Distribution information
IL, MN, & WI
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: E-Mail.
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.