Skip to main content

Blue Diamond Growers Recall: 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.

United States

TerminatedClass I

Company
Blue Diamond Growers
Product
Whole Brown Almonds (bulk)
Recall date
August 5, 2022
Terminated
October 17, 2022
Source
FDA

Reason for recall

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.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Whole Brown Almonds (bulk) Not published in this source record 347,650 lbs 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

Distribution

  • U.S distribution to the following California
  • Colorado
  • and Illinois Foreign distribution to the following: Germany
  • Morocco
  • and Canada

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-1559-2022
Event ID
90721
Status
Terminated
Classification
Class I
Company
Blue Diamond Growers
Product description
Whole Brown Almonds (bulk)
Quantity
347,650 lbs
Reason
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.
Recall initiation date
August 5, 2022
Report date
August 24, 2022
Classification date
Not published in this source record
Termination date
October 17, 2022
Distribution pattern
U.S distribution to the following California, Colorado, and Illinois Foreign distribution to the following: Germany, Morocco, and Canada
UPC, lot, and code information
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
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
E-Mail
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: Blue Diamond Growers

Other recalls from Blue Diamond Growers

FDA Recall United States Terminated Historical recordClass I

Blue Diamond Growers

Product
Blue Diamond Almonds Blanc DCD FN C (blanched diced fine);…
Published
June 28, 2017
Distribution
Multiple states

View recall →

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class I mean?

A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.