CLASS II Food recall · Reported 24 Sep 2014 · FDA Enforcement Report

JSF Ground Tuna - IQF - Origin: Indonesia -, frozen recalled

Japanese Specialty Food Distributors is recalling JSF Ground Tuna - IQF - Origin: Indonesia -, frozen, distributed in Connecticut, Georgia, New Jersey, New York, Texas. The recall was initiated on 21 Jul 2014 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesAll lots
Quantity recalled961 cases

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-2443-2014
FDA event ID
68861
Recalling firm
Japanese Specialty Food Distributors, Brookfield, CT
Classification
Class II
Status
Terminated
Recall initiated
21 Jul 2014
FDA classified
16 Sep 2014
Reported
24 Sep 2014
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Other Reasons
Product category
Tuna

Timeline

21 Jul 2014Recall initiated by company
16 Sep 2014Classified by FDA+57 days
24 Sep 2014Published in enforcement report+8 days

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

Reason for recall

Product associated with scombroid illness.

Product as listed by the FDA

JSF Ground Tuna - IQF - Origin: Indonesia - 2/11LB, frozen

Where it was distributed

Product was distributed directly to CT, NY, NJ, TX, and GA

ConnecticutGeorgiaNew JerseyNew YorkTexas

Questions about this recall

Why was it recalled?

Product associated with scombroid illness.

Which lots are affected?

All lots

Where was it sold?

Product was distributed directly to CT, NY, NJ, TX, and GA

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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