Recall record at a glance
| Official record | F-1025-2015 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | Kkot Saem Bean Sprouts |
| Report date | Feb 18, 2015 |
| Recall initiation date | Dec 19, 2014 |
| Quantity | 8851.5 lbs. |
| Location | Spanaway, WA, United States |
Official product description
Soybean Sprouts, net wt. 1.5 lbs., sold under brand Winter Blossom Bean Sprouts brand. Product is packaged in plastic bag, multi-colored with orange stripe on top, lower middle portion and at bottom. The orange & black English and Korea letters on white background on front of bag. the UPC is 0 94922 55330 0. Soybean Sprouts, net wt. 5 lbs., sold in clear bag with no label. There is no UPC for this product.
Why the product was recalled
Soybean Sprouts are recalled because it has the potential to be contaminated with Listeria monocytogenes.
Distribution information
Distributed in Oregon and Washington
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: Press Release.
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.