Recall record at a glance
| Official record | F-1812-2016 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | CRF Frozen Foods, LLC |
| Report date | Aug 3, 2016 |
| Recall initiation date | May 2, 2016 |
| Quantity | 401,928 lbs |
| Location | Pasco, WA, United States |
Official product description
Organic Chopped Kale, Brand Bybee Foods, Net Wt 56 oz, UPC 4635800054 Organic Chopped Kale, Brand Organic by Nature, Net Wt 40 lb, UPC R02208 Chopped Kale, Brand O Organic, Net Wt 10 oz, UPC 7989340282 Organic Chopped Kale, Brand Wild Oats, Net Wt 10 oz, UPC 4873700379 *******BULK containers***************** Organic Kale, Brand Pacific Foods, Net Wt. 40 lbs
Why the product was recalled
Chopped Kale are recalled because they have the potential to be contaminated with Listeria monocytogenes.
Distribution information
US nationwide and in Canada & Japan.
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.