Check the Batch
Class IITerminated in FDA datasetRecall initiated Sep 3, 2016

Southern Grove Cashews with Sea Salt, a 10 ounce stand up pouch bag with a

Recalling firm: Kanan Enterprises, Inc.

Why it was recalled

This recall has been initiated due to the possible presence of peanuts.

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Dec 20, 2016.

Check your package

Compare the exact product and package details with the label you have.

ProductSouthern Grove Cashews with Sea Salt, a 10 ounce stand up pouch bag with a UPC 0 38445 12286 5 and the date codes of Best By May 24 2017 KN and August 05 2017 KN
Package size10 ounce
UPC038445122865

FDA code information

UPC 0 38445 12286 5 and the date codes of Best By May 24 2017 KN and August 05 2017 KN.

Match the product, package size, and code together. A missing match does not guarantee safety.

Full FDA record and distribution details

Original product description

Southern Grove Cashews with Sea Salt, a 10 ounce stand up pouch bag with a UPC 0 38445 12286 5 and the date codes of Best By May 24 2017 KN and August 05 2017 KN

Extracted codes and context

TypeCode / valueContext
UPC038445122865UPC 0 38445 12286 5 and the date codes of Best By May 24 2017 KN and August 05 2017 KN.
UPC038445122865Southern Grove Cashews with Sea Salt, a 10 ounce stand up pouch bag with a UPC 0 38445 12286 5 and the date codes of Best By May 24 2017 KN and August 05 2017 KN
best byMay 24 2017UPC 0 38445 12286 5 and the date codes of Best By May 24 2017 KN and August 05 2017 KN.
best byMay 24 2017nce stand up pouch bag with a UPC 0 38445 12286 5 and the date codes of Best By May 24 2017 KN and August 05 2017 KN

Original FDA recall reason

This recall has been initiated due to the possible presence of peanuts.

Recall details

Recall number
F-2330-2016
Event ID
75109
FDA status
Terminated
Initiated
Sep 3, 2016
Reported
Sep 28, 2016
Classified
Sep 16, 2016
Terminated
Dec 20, 2016
Quantity
485 cases (7760 individual bags)
Location
Solon, OH, United States
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

US nationwide. The product was distributed to the following states: OH, KS, MN.

FDA source record · F-2330-2016

Data updated September 16, 2026. View official FDA data ↗

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