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Lower risk Food recall · FDA · Published June 2, 2017

Star Snacks Cashew Halves Recall: Glass Fragments Found in Product

Star Snacks recalls 8oz cashew halves with sea salt due to glass fragments found in some products. Consumers should check UPC code 041498179366 and discard if affected.

🇺🇸 FDA recall #F-2390-2017FoodStar Snacks ›
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Recalling firmStar Snacks Co., Llc.105 Harbor Dr · Jersey City, NJ 07305-4505
✎ GovInfoNow plain-language explainer

What happened, in plain English

Star Snacks is recalling 8-ounce cashew halves with sea salt because glass fragments were found in some products. This could cause injury if the glass cuts the mouth or throat during eating. Read more at govinfonow.com/recall/21144-star-snacks-cashew-halves-recall-glass-fragments-found-in-product.

Source Summary by GovInfoNow · govinfonow.com/recall/21144-star-snacks-cashew-halves-recall-glass-fragments-found-in-product · Updated October 8, 2026 · FDA enforcement record: FDA #F-2390-2017

Cite this page

“Star Snacks Cashew Halves Recall: Glass Fragments Found in Product.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/21144-star-snacks-cashew-halves-recall-glass-fragments-found-in-product. Based on FDA recall #F-2390-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-2390-2017%22&limit=1).

Why it’s dangerous

Glass fragments can cause cuts or lacerations in the mouth or throat if the product is eaten. The glass came from unknown sources and was likely present in the raw materials before packaging.

Who’s affected

Anyone who bought Star Snacks Southern Grove Cashew Halves & Pieces with Sea Salt, 8.0 oz. (227 grams) with UPC 041498179366 before November 27, 2018. Children and people with sensitive mouths are at slightly higher risk.

How to tell if you have this one

Check for the UPC code 041498179366 on the product label. The product was sold with a best by date of November 27, 2018 (27B7 936 3).

  • Brand
    Star Snacks
  • Product
    Southern Grove Cashew Halves & Pieces with Sea Salt, Net Weight 8.0 oz. (227 grams)
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Label

    Look for the UPC code 041498179366 on the package.

  2. Discard if Affected

    If you have the product with the UPC code 041498179366, discard it immediately to avoid injury.

Where it went and when

Where it was distributed

Distributed in Michigan.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: not listedWIMichigan: yesMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: not listedTXFlorida: not listedFL

FDA distribution: “ALDI Distribution Centers. 3/6/2017 Hinckly OH 3/6/2017 Hanes City FL 3/8/2017 Frederick MD 3/8/2017 OFallon MO 3/28/2017 OFallon MO 3/28/2017 Frederick MD 4/3/2017 Hinckly OH 4/3/2017 Salisbury NC 4/3/2017 Batavia IL 4/6/2017 Frederick…” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Michigan.

Recall timeline

FDA terminated this recall 8 months after the firm started it.

1. Firm started the recall: Jun 2, 201712. FDA classified it Class II: Jun 22, 201723. Published in FDA’s Enforcement Report: Jun 28, 201734. FDA terminated the recall: Feb 1, 2018420172018
  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.

✎ GovInfoNow

Questions people ask

Is there a fix for this issue?

No fix is available; the product must be discarded if it has the recalled UPC code.

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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-2390-2017 (June 2, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-2390-2017 to see it in context.
  • Plain-language summary written by qwen3:4b on October 8, 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