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Stop using now Food recall · FDA · Published January 12, 2018

Gobugi Dried Anchovies Risk Botulism Contamination - Recall

Gobugi Holdings recalls dried anchovies (S, M, L) due to potential Clostridium botulinum contamination. Products sold in 1.5kg cardboard boxes without brand names. Consumers should check UPCs and contact the company for details.

🇺🇸 FDA recall #F-0828-2018FoodGobugi Holdings ›
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Contact the company

Recalling firmGobugi Holdings Inc4520 Sw 110th Ave · Beaverton, OR 97005-3011
✎ GovInfoNow plain-language explainer

What happened, in plain English

Gobugi Holdings is recalling dried anchovies in small, medium, and large sizes sold in 1.5kg cardboard boxes without brand names. The product may be contaminated with Clostridium botulinum, a bacterium that can cause botulism, a serious foodborne illness. Read more at govinfonow.com/recall/19806-gobugi-dried-anchovies-risk-botulism-contamination-recall.

Source Summary by GovInfoNow · govinfonow.com/recall/19806-gobugi-dried-anchovies-risk-botulism-contamination-recall · Updated October 7, 2026 · FDA enforcement record: FDA #F-0828-2018

Cite this page

“Gobugi Dried Anchovies Risk Botulism Contamination - Recall.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/19806-gobugi-dried-anchovies-risk-botulism-contamination-recall. Based on FDA recall #F-0828-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0828-2018%22&limit=1).

Why it’s dangerous

Dried anchovies may contain Clostridium botulinum, a bacterium that produces a toxin causing botulism. This illness can lead to muscle weakness, paralysis, and even death if not treated promptly. The product's packaging does not include a brand name, making it difficult to identify.

Who’s affected

Anyone who purchased dried anchovies from Gobugi Holdings in the U.S. or Canada. People with compromised immune systems are at higher risk for botulism.

How to tell if you have this one

Check for products labeled with UPC 4 98900 00146 1 (small), 4 98900 00149 2 (medium), or 4 98900 00148 5 (large). Products sold in 1.5kg cardboard boxes without brand names.

  • Brand
    Gobugi Holdings
  • Product
    Dried Anchovy, size (S), (M), (L), packaged in 1.5 kg. cardboard box without brand name. The cardboard box states
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Stop Using Now

    Immediately discard any recalled dried anchovies to avoid potential botulism poisoning.

Where it went and when

Where it was distributed

Distributed in California and Oregon.

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: yesORNevada: 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: “Distributed in California and Oregon” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: California, Oregon.

Recall timeline

FDA terminated this recall 6 months after the firm started it.

1. Firm started the recall: Jan 12, 201812. FDA classified it Class II: Feb 21, 201823. Published in FDA’s Enforcement Report: Feb 28, 201834. FDA terminated the recall: Jul 27, 201842018
  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-0828-2018 (January 12, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0828-2018 to see it in context.
  • Plain-language summary written by qwen3:4b on October 7, 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