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Stop using now Food recall · FDA · Published February 25, 2017

Fuji Food Recalls Hawaiian Delight Due to Listeria Risk

Fuji Food Products recalls 4.5lb Hawaiian Delight due to potential Listeria monocytogenes contamination. Check your fridge for the specific sell-by date.

🇺🇸 FDA recall #F-1778-2017FoodFuji Food Products ›
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Contact the company

Recalling firmFuji Food Products, Inc.14420 Bloomfield Ave · Santa Fe Springs, CA 90670-5410
✎ GovInfoNow plain-language explainer

What happened, in plain English

Fuji Food Products, Inc. is recalling its 4.5-pound package of Hawaiian Delight because it may be contaminated with Listeria monocytogenes. This is a Class I recall, which indicates a serious health risk or death could result from eating the product. The affected items were sold in California. Read more at govinfonow.com/recall/22165-fuji-food-recalls-hawaiian-delight-due-to-listeria-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/22165-fuji-food-recalls-hawaiian-delight-due-to-listeria-risk · Updated October 11, 2026 · FDA enforcement record: FDA #F-1778-2017

Cite this page

“Fuji Food Recalls Hawaiian Delight Due to Listeria Risk.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/22165-fuji-food-recalls-hawaiian-delight-due-to-listeria-risk. Based on FDA recall #F-1778-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1778-2017%22&limit=1).

Why it’s dangerous

Listeria monocytogenes is a bacterium that can cause serious infections, particularly dangerous for pregnant women, older adults, and people with weakened immune systems. Ingesting contaminated food can lead to severe illness or death.

Who’s affected

Consumers in California who purchased the 4.5-pound packages of Hawaiian Delight with the specific sell-by date and UPC listed in the record.

How to tell if you have this one

Look for Hawaiian Delight packages with a net weight of 4.5lb. Check the Sell By Date of 04/11/17 and the UPC code 6360340004. The product was distributed in California.

  • Brand
    Fuji Food Products
  • Product
    Hawaiian Delight, Net Wt. 4.5lb
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Stop consuming the product

    Do not eat the Hawaiian Delight if you have it at home due to the Listeria risk.

  2. Discard or return the item

    The record does not specify a specific remedy like a refund or replacement, so consumers should dispose of the product safely.

Where it went and when

Where it was distributed

Distributed in California.

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: 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: 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: 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: “US: CA” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: California.

Recall timeline

FDA terminated this recall 31 days after the firm started it.

1. Firm started the recall: Feb 25, 201712. FDA classified it Class I: Mar 28, 201723. FDA terminated the recall: Mar 28, 201734. Published in FDA’s Enforcement Report: Apr 5, 201742017
  1. Firm started the recall
  2. FDA classified it Class I
  3. FDA terminated the recall
  4. Published in FDA’s Enforcement Report

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-1778-2017 (February 25, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1778-2017 to see it in context.
  • Plain-language summary written by qwen3.6:35b-a3b on October 11, 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