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Stop using now Food recall · FDA · Published June 20, 2016

Al Rasheed Sardines Recalled for Botulism Risk

Greenland Trading Corp recalls Al Rasheed Sardines (Item #4017) due to potential C. botulinum contamination. Check your pantry.

🇺🇸 FDA recall #F-1924-2016FoodAl Rasheed ›
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Recalling firmGreenland Trading Corp238 Pennsylvania Ave · Paterson, NJ 07503-2121
✎ GovInfoNow plain-language explainer

What happened, in plain English

Greenland Trading Corporation is recalling Al Rasheed Sardines, specifically Item #4017, because of a potential risk of Clostridium botulinum contamination. This Class I recall affects 106 cases, with each case containing 24 packages. The products were distributed in California, Florida, Massachusetts, New Jersey, New York, Pennsylvania, and Tennessee. Read more at govinfonow.com/recall/23938-al-rasheed-sardines-recalled-for-botulism-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/23938-al-rasheed-sardines-recalled-for-botulism-risk · Updated October 9, 2026 · FDA enforcement record: FDA #F-1924-2016

Cite this page

“Al Rasheed Sardines Recalled for Botulism Risk.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/23938-al-rasheed-sardines-recalled-for-botulism-risk. Based on FDA recall #F-1924-2016 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1924-2016%22&limit=1).

Why it’s dangerous

The product may be contaminated with Clostridium botulinum, a bacterium that produces a toxin causing botulism. This toxin attacks the body's nerves and can lead to severe neurological symptoms and potentially fatal respiratory failure.

Who’s affected

Consumers who purchased Al Rasheed Sardines Item #4017 in the affected states are at risk. Botulism is a serious illness that can cause paralysis and death if untreated.

How to tell if you have this one

Look for Al Rasheed Sardines, Item #4017. The record notes that the label was not available during NYSDAM sampling in March 2017. Check if you purchased these items in CA, FL, MA, NJ, NY, PA, or TN.

  • Brand
    Al Rasheed
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Stop consuming immediately

    Do not eat the product due to the risk of botulism contamination.

  2. Discard or return product

    The record does not specify a remedy, so you should dispose of the item or contact the retailer for guidance.

Where it went and when

Where it was distributed

Distributed in 7 states.

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: not listedMINew York: yesNYRhode Island: not listedRIMassachusetts: yesMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: yesPANew Jersey: yesNJConnecticut: not listedCTCalifornia: yesCAUtah: 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: yesTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: not listedTXFlorida: yesFL

FDA distribution: “CA, FL, MA, NJ, NY, PA and TN” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: California, Florida, Massachusetts, New Jersey, New York, Pennsylvania, Tennessee.

Recall timeline

FDA terminated this recall 3 months after the firm started it.

1. Firm started the recall: Jun 20, 201612. FDA classified it Class I: Aug 15, 201623. Published in FDA’s Enforcement Report: Aug 24, 201634. FDA terminated the recall: Sep 21, 201642016
  1. Firm started the recall
  2. FDA classified it Class I
  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-1924-2016 (June 20, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1924-2016 to see it in context.
  • Plain-language summary written by qwen3.6:35b-a3b 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