Recall record at a glance
| Official record | F-1559-2022 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | Blue Diamond Growers |
| Report date | Aug 24, 2022 |
| Recall initiation date | Aug 5, 2022 |
| Quantity | 347,650 lbs |
| Location | Sacramento, CA, United States |
Official product description
Whole Brown Almonds (bulk)
Why the product was recalled
Firm's internal sampling identified a positive Salmonella result on Item 00113 that was on hand at the firm on 7/15/2022. Firm elected to hold all inventory between the sanitation break from 7/5/2022 - 7/18/2022. Some product from within that time frame was shipped to customers. Although none of the products on the recall list tested positive for Salmonella, out of an abundance of caution the firm elected to proceed with a recall on the shipped products.
Distribution information
U.S distribution to the following California, Colorado, and Illinois Foreign distribution to the following: Germany, Morocco, and Canada
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.