Recall record at a glance
| Official record | F-1011-2018 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | Bob's Red Mill Natural Foods, Inc. |
| Report date | Apr 18, 2018 |
| Recall initiation date | Apr 6, 2018 |
| Quantity | 2099 cases |
| Location | Milwaukie, OR, United States |
Official product description
Amaranth Flour, Organic Whole Grain, Item Number: 6001C224, Net wt. 22 oz. UPC 0 39978 00911 1. The label is read in parts: "***Bob's Red Mill ***ORGANIC WHOLE GRAIN AMARANTH FLOUR STONE GROUND*** NET WT 22 OZ ***keeps best refrigerated or frozen***".
Why the product was recalled
Amaranth Flour is recalled due to potential for contamination with Salmonella.
Distribution information
Distributed in CA, FL, MI, ND, NH, NY, OH, OR, TX, and WA and in Mexico and United Arab Emirates.
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: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.
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.