CLASS II Food recall · Reported 20 Nov 2019 · FDA Enforcement Report

Trade Winds Premium Grade Yellowfin (Ahi) Tuna Ground Keep Frozen recalled

Relish Foods is recalling Trade Winds Premium Grade Yellowfin (Ahi) Tuna Ground Keep Frozen, distributed in New York. The recall was initiated on 11 Oct 2019 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLOT # 19109 Best By 04/19/2021
Quantity recalled600 cases - 6000 lbs.

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-0138-2020
FDA event ID
84048
Recalling firm
Relish Foods, Culver City, CA
Classification
Class II
Status
Terminated
Recall initiated
11 Oct 2019
FDA classified
8 Nov 2019
Reported
20 Nov 2019
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Other Reasons
Product category
Sauces & Condiments

Timeline

11 Oct 2019Recall initiated by company
8 Nov 2019Classified by FDA+28 days
20 Nov 2019Published in enforcement report+12 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Positive for histamine level at 140 ppm.

Product as listed by the FDA

Trade Winds Premium Grade Yellowfin (Ahi) Tuna Ground Keep Frozen Net Weight 10 LBS. (4.54 KG) Product of Vietnam Specifically Packed For: Relish Foods, Inc. 5840 Uplander Way #201 Culver City, CA 90230

Where it was distributed

U.S. distribution to NY. No foreign distribution.

New York

Questions about this recall

Why was it recalled?

Positive for histamine level at 140 ppm.

Which lots are affected?

LOT # 19109 Best By 04/19/2021

Where was it sold?

U.S. distribution to NY. No foreign distribution.

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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