Recall archive / FDA food enforcement
FreshPoint Bix Produce Company, Whole Cantaloupe, Item 03143. 1/3 CT. 3 melons per container. — FDA record F-0665-2024
Reported terminated
Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.
Source date Nov 17, 2023. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
What the record says
- Product
- FreshPoint Bix Produce Company, Whole Cantaloupe, Item 03143. 1/3 CT. 3 melons per container.
- Reason
- Potential Salmonella contamination.
- Classification
- Class I
- Recalling firm
- FreshPoint Bix Produce Company, LLC
- Quantity
- 186 packs
- Agency-reported status
- Terminated
- Source record identifier
- F-0665-2024
What the recall classes mean. Classification is an agency assessment, not individual medical advice.
Lot and product identifiers
| Label field | Details supplied by the agency |
|---|---|
| Lot, code or applicability | Lot number / Sales Order #: 05969898, 05969922, 05970496, 05970946, 05971028, 05971138, 05971525, 05971594, 05971721, 05971831, 05971950, 05971967, 05972082, 05972083, 05972121, 05972148, 05972324, 05972643, 05972986, 05972996, 05973042, 05973100, 05973147, 05973252, 05973373, 05973448, 05973449, 05973489, 05973539, 05973578, 05973591, 05973596, 05973630, 05973667, 05973685, 05973860, 05974017, 05974106, 05974133, 05974245, 05974253, 05974307, 05974325, 05974444, 05974496, 05974512, 05974525, 05974552, 05974602, 05974914, 05974937, 05974946, 05974984, 05977048, 05977062, 05977359, 05977394, 05977462, 05977558, 05977562, 05977597, 05977724, 05977745, 05977838, 05977859, 05978068, 05978074, 05978140, 05978205, 05978300, 05978388, 05978646, 05978674, 05978784, 05978805, 05978810, 05978820, 05978893, 05978903, 05978939, 05978981, 05979066, 05979117, 05979134, 05979328, 05979380, 05979464, 05979509, 05979667, 05980158, 05980284, 05980375, 05980606, 05980622, 05980722, 05980767, 05980824, 05981102, Lot number / Sales Order # from 11/28/2023 notification: 05964131, 05965851, 05966808, 05967056, 05967401, 05967678, 05967771, 05968514, 05968566, 05968633, 05968652, 05968692, 05968721, 05968729, 05968730, 05968816, 05968868, 05968909, 05968985, 05969032, 05969090, 05969187, 05969202, 05969232, 05969653, 05969727, 05969879, 05969998, 05970039, 05970168, 05970187, 05970243, 05970299, 05970343, 05970388, 05970395, 05970411, 05970543, 05970762, 05970889, 05970963, 05971095, 05971142, 05971160, 05971275, 05971301, 05971386, 05971643, 05971739, 05971812, 05971818, 05971897, 05971990, 05971998, 05972008, 05972126, 05972149, 05972261, 05972290, 05972497. |
Match all identifying details in the current notice. A brand name alone is not enough.
Distribution
IA, MN, ND, WI
States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.
Dates in the source
- Report date
- Dec 13, 2023
- Recall initiation date
- Nov 17, 2023
- Center classification date
- Jan 2, 2024
- Termination date
- Jan 15, 2025
FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.