Recall record at a glance
| Official record | F-0183-2022 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | POTANDON PRODUCE LLC |
| Report date | Nov 24, 2021 |
| Recall initiation date | Oct 25, 2021 |
| Quantity | Total 61,206 lbs or 359 cases (25/2 lb. pkg per case); 397 cases (16/3 lb. pkg per case); 484 cases (10/5 lb. pkg per case); |
| Location | Idaho Falls, ID, United States |
Official product description
Green Giant Fresh brand, Whole YELLOW Onions packaged in 2 lb. flexible mesh bags, UPC 60580600120-8. Green Giant Fresh brand, Whole YELLOW Onions packaged in 3 lb. flexible mesh bags, UPC 60580600123-9. Green Giant Fresh brand, Whole YELLOW Onions packaged in 5 lb. flexible mesh bags, UPC 60580600170-3.
Why the product was recalled
Salmonella Oranienburg. Products are supplied by Keeler Family Farm.
Distribution information
distributed in MN and ND.
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.