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Stop using now Food recall · FDA · Published October 11, 2019

Trade Winds Yellowfin Tuna Recall: High Histamine Risk

Relish Foods recalls Trade Winds Premium Grade Yellowfin Tuna Ground due to elevated histamine levels. Check your freezer for affected lots immediately.

🇺🇸 FDA recall #F-0138-2020FoodTrade Winds ›
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Recalling firmRelish Foods, Inc. dba Gourmet Fusion Foods, Inc.5840 Uplander Way Ste 201 · Culver City, CA 90230-6637
✎ GovInfoNow plain-language explainer

What happened, in plain English

Relish Foods, Inc. is recalling Trade Winds Premium Grade Yellowfin (Ahi) Tuna Ground because it tested positive for high histamine levels at 140 ppm. This product was distributed in the U.S., specifically to New York. Consumers should check their freezers for this specific item. Read more at govinfonow.com/recall/16513-trade-winds-yellowfin-tuna-recall-high-histamine-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/16513-trade-winds-yellowfin-tuna-recall-high-histamine-risk · Updated October 11, 2026 · FDA enforcement record: FDA #F-0138-2020

Cite this page

“Trade Winds Yellowfin Tuna Recall: High Histamine Risk.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/16513-trade-winds-yellowfin-tuna-recall-high-histamine-risk. Based on FDA recall #F-0138-2020 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0138-2020%22&limit=1).

Why it’s dangerous

The product contains histamine levels at 140 ppm, which can cause scombroid poisoning or other adverse health reactions when consumed. High histamine in fish indicates spoilage or improper temperature control during processing or storage.

Who’s affected

Consumers in New York who purchased frozen tuna from retailers distributing Relish Foods products are likely affected. Individuals who consume seafood may be at risk of histamine-related illness if the product is eaten.

How to tell if you have this one

Look for Trade Winds Premium Grade Yellowfin (Ahi) Tuna Ground, kept frozen, with a net weight of 10 LBS. (4.54 KG). Check the label for LOT # 19109 and a Best By date of 04/19/2021. The packaging states 'Product of Vietnam' and 'Specifically Packed For: Relish Foods, Inc.'

  • Brand
    Trade Winds
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Stop consuming the product

    Do not eat the recalled tuna due to the risk of high histamine levels.

  2. Discard or return the item

    The recall record does not specify a remedy, so please contact the manufacturer or retailer for instructions on disposal or refund.

Where it went and when

Where it was distributed

Distributed in New York.

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: 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: “U.S. distribution to NY. No foreign distribution.” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: New York.

Recall timeline

FDA terminated this recall 4 months after the firm started it.

1. Firm started the recall: Oct 11, 201912. FDA classified it Class II: Nov 8, 201923. Published in FDA’s Enforcement Report: Nov 20, 201934. FDA terminated the recall: Feb 21, 2020420192020
  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

Where was this product sold?

The product was distributed in the U.S. to New York, with no foreign distribution.

How much of this product was recalled?

Approximately 600 cases, totaling 6000 lbs. of product were recalled.

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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-0138-2020 (October 11, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0138-2020 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