Whole Brown Almonds (Blue Diamond) – Salmonella Risk (2022)
Class I: A situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death
Class I recall indicates potential for serious health consequences.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Whole Brown Almonds (bulk)
Brand
Blue Diamond Growers
Lot Codes / Batch Numbers
Item - 14233, Batch 1000223917 of Lot 186224001, Item 14233 - Batch 1000223941 of Lot 187224001, Item 14203 - Batch 1000223938 of Lot 187224001, Item 14428 - Batch 1000223977 of Lot 188224001, Item 14427 - Batch 1000224058 of Lot 191224001, Item - 14237, Batch 1000224066 of Lot 191224001, Item- 14237, Batch 1000224071 of Lot 192224001, Item - 00100, Batch 1000224159 of Lot 193224001, Item - 00100, Batch 1000224193 of Lot 194224001, and Item - 14197, Batch 1000224233 of Lot 195224001
Products Sold
Item - 14233, Batch 1000223917 of Lot 186224001; Item 14233 - Batch 1000223941 of Lot 187224001; Item 14203 - Batch 1000223938 of Lot 187224001; Item 14428 - Batch 1000223977 of Lot 188224001; Item 14427 - Batch 1000224058 of Lot 191224001; Item - 14237, Batch 1000224066 of Lot 191224001; Item- 14237, Batch 1000224071 of Lot 192224001; Item - 00100, Batch 1000224159 of Lot 193224001; Item - 00100, Batch 1000224193 of Lot 194224001; and Item - 14197,Batch 1000224233 of Lot 195224001
Blue Diamond Growers is recalling Whole Brown Almonds (bulk) due to 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 in. This is a Class I recall, indicating a high risk of serious health consequences. Based on FDA enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
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.
Recommended Action
Per FDA guidance
Consumers should stop using the product and contact the recalling firm or return it to the place of purchase.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
CA, CO, IL
Page updated: Jan 6, 2026