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Stop using now Food recall · FDA · Published June 4, 2018

Pacific Brand Charcoal Grilled Eel Recall: Mebendazole Found

Supreme Foods recalls Pacific Brand Charcoal Grilled Eel due to Mebendazole contamination. Check lot codes and expiry dates for affected products.

🇺🇸 FDA recall #F-1596-2018FoodPacific ›
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Recalling firmSupreme Foods3219 Durfee Ave · El Monte, CA 91732-3217
✎ GovInfoNow plain-language explainer

What happened, in plain English

Supreme Foods is recalling Pacific Brand Charcoal Grilled Eel because FDA inspections found the drug Mebendazole in two imported shipments that should have been held. The product was distributed in California, New Jersey, Texas, and Washington. The recall covers specific lots with expiry dates in October and December 2019. Read more at govinfonow.com/recall/19069-pacific-brand-charcoal-grilled-eel-recall-mebendazole-found.

Source Summary by GovInfoNow · govinfonow.com/recall/19069-pacific-brand-charcoal-grilled-eel-recall-mebendazole-found · Updated October 11, 2026 · FDA enforcement record: FDA #F-1596-2018

Cite this page

“Pacific Brand Charcoal Grilled Eel Recall: Mebendazole Found.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/19069-pacific-brand-charcoal-grilled-eel-recall-mebendazole-found. Based on FDA recall #F-1596-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1596-2018%22&limit=1).

Why it’s dangerous

The hazard is the presence of Mebendazole amine, a drug that should not be in this food product. The FDA found this substance in shipments that were supposed to be held back from distribution due to import alerts.

Who’s affected

Consumers who purchased Pacific Brand Charcoal Grilled Eel from stores in California, New Jersey, Texas, or Washington are affected. Individuals who have the specific lot codes listed below are at risk of ingesting a prohibited substance.

How to tell if you have this one

Check your package for the UPC 692156201099 and look for one of two lot codes: EXP20191022 (Expiry Date: Oct 22 2019) or EXP20191214 (Expiry Date: Dec 12 2019). The product is labeled as 'Premium Quality Unagi Kabayaki'.

  • Brand
    Pacific
  • Product
    Pacific Brand Charcoal Grilled Eel. Premium Quality Unagi Kabayaki UPC: 692156201099
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check your product

    Verify if your Pacific Brand Charcoal Grilled Eel matches the UPC and lot codes listed in the recall.

  2. Stop consuming the product

    Do not eat the recalled eel if it matches the identified lots due to potential drug contamination.

Where it went and when

Where it was distributed

Distributed in 4 states.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: yesWAIdaho: 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: 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: not listedTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: yesTXFlorida: not listedFL

FDA distribution: “CA, NJ, TX, WA” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: California, New Jersey, Texas, Washington.

Recall timeline

FDA terminated this recall 12 months after the firm started it.

1. Firm started the recall: Jun 4, 201812. FDA classified it Class III: Jun 27, 201823. Published in FDA’s Enforcement Report: Jul 4, 201834. FDA terminated the recall: Jun 18, 2019420182019
  1. Firm started the recall
  2. FDA classified it Class III
  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-1596-2018 (June 4, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1596-2018 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