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Lower risk Food recall · FDA · Published September 3, 2016

Southern Grove Cashews with Sea Salt Recall: Possible Peanuts in Product

Kanan Enterprises recalls Southern Grove Cashews with Sea Salt pouches due to possible peanut contamination. Affected items have specific UPC and date codes. Consumers should check their products and avoid if allergic.

🇺🇸 FDA recall #F-2330-2016FoodKanan Enterprises ›
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Recalling firmKanan Enterprises, Inc.31900 Solon Rd · Solon, OH 44139-3536
✎ GovInfoNow plain-language explainer

What happened, in plain English

Kanan Enterprises is recalling Southern Grove Cashews with Sea Salt pouches because they may contain peanuts. This poses a risk for people with peanut allergies. The recall includes specific UPC and date codes. Read more at govinfonow.com/recall/23270-southern-grove-cashews-with-sea-salt-recall-possible-peanuts-in.

Source Summary by GovInfoNow · govinfonow.com/recall/23270-southern-grove-cashews-with-sea-salt-recall-possible-peanuts-in · Updated October 9, 2026 · FDA enforcement record: FDA #F-2330-2016

Cite this page

“Southern Grove Cashews with Sea Salt Recall: Possible Peanuts in Product.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/23270-southern-grove-cashews-with-sea-salt-recall-possible-peanuts-in. Based on FDA recall #F-2330-2016 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-2330-2016%22&limit=1).

Why it’s dangerous

The product may contain peanuts, which can cause allergic reactions in sensitive individuals. This is a potential hazard for people with peanut allergies, but the recall does not indicate a risk of serious injury beyond allergic reactions.

Who’s affected

People with peanut allergies are at risk from this product. The recall affects consumers who purchased the specific Southern Grove Cashews with Sea Salt pouches with the listed UPC and date codes.

How to tell if you have this one

Check for the UPC 0 38445 12286 5 on the pouch. The date codes are Best By May 24, 2017 and August 05, 2017.

  • Brand
    Kanan Enterprises
  • Product
    Kanan Enterprises, Inc. recalls 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
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Look for the UPC 0 38445 12286 5 and date codes Best By May 24, 2017 and August 05, 2017 on the pouch.

Where it went and when

Where it was distributed

Distributed nationwide; the notice names 3 states.

Alaska: nationwideAKMaine: nationwideMEVermont: nationwideVTNew Hampshire: nationwideNHWashington: nationwideWAIdaho: nationwideIDMontana: nationwideMTNorth Dakota: nationwideNDMinnesota: named in the noticeMNIllinois: nationwideILWisconsin: nationwideWIMichigan: nationwideMINew York: nationwideNYRhode Island: nationwideRIMassachusetts: nationwideMAOregon: nationwideORNevada: nationwideNVWyoming: nationwideWYSouth Dakota: nationwideSDIowa: nationwideIAIndiana: nationwideINOhio: named in the noticeOHPennsylvania: nationwidePANew Jersey: nationwideNJConnecticut: nationwideCTCalifornia: nationwideCAUtah: nationwideUTColorado: nationwideCONebraska: nationwideNEMissouri: nationwideMOKentucky: nationwideKYWest Virginia: nationwideWVVirginia: nationwideVAMaryland: nationwideMDDelaware: nationwideDEArizona: nationwideAZNew Mexico: nationwideNMKansas: named in the noticeKSArkansas: nationwideARTennessee: nationwideTNNorth Carolina: nationwideNCSouth Carolina: nationwideSCDistrict of Columbia: nationwideDCOklahoma: nationwideOKLouisiana: nationwideLAMississippi: nationwideMSAlabama: nationwideALGeorgia: nationwideGAHawaii: nationwideHITexas: nationwideTXFlorida: nationwideFL

FDA distribution: “US nationwide. The product was distributed to the following states: OH, KS, MN.” States read from FDA’s own wording; “not listed” means the notice does not name it.

Named in the notice: Kansas, Minnesota, Ohio.

Recall timeline

FDA terminated this recall 4 months after the firm started it.

1. Firm started the recall: Sep 3, 201612. FDA classified it Class II: Sep 16, 201623. Published in FDA’s Enforcement Report: Sep 28, 201634. FDA terminated the recall: Dec 20, 201642016
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #F-2330-2016 (September 3, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-2330-2016 to see it in context.
  • Plain-language summary written by qwen3:4b on October 9, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA