Recall record at a glance
| Official record | F-0101-2021 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | Meijer Inc./Traffic Dept. |
| Report date | Nov 18, 2020 |
| Recall initiation date | Oct 5, 2020 |
| Quantity | 44428 units |
| Location | Grand Rapids, MI, United States |
Official product description
FRESH FROM MEIJER MIXED MELON SLICES, 24oz Clear plastic container, UPC 220220600075. FRESH FROM MEIJER MIXED MELON CHUNKS LARGE BOWL, 32oz Clear plastic container, UPC 219334109727. FRESH FROM MEIJER MIXED MELON CHUNKS SMALL BOWL, 16oz Clear plastic container, UPC 219337109724. FRESH FROM MEIJER GS MIXED MELON CUP 6 OZ, 6oz Clear plastic container, UPC 219718601397. FRESH FROM MEIJER MIXED MELON CUP, 6oz Clear plastic container, UPC 219844101174. FRESH FROM MEIJER GS MIXED MELON CUP 6 OZ, 6oz Clear plastic container, (GAS STATIONS), UPC 219718601397, PLU 9450.
Why the product was recalled
potential risk of Salmonella
Distribution information
Meijer stores in Michigan, Ohio, Indiana, Illinois, Kentucky and Wisconsin.
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.