CLASS II Food recall · Reported 26 Dec 2012 · FDA Enforcement Report

Frozen Tuna Loins 3/5 recalled by Unified Seafood Company

Unified Seafood is recalling Frozen Tuna Loins 3/5, distributed nationwide in the US. The recall was initiated on 23 Oct 2012 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot and (Code): 93514 (436-9) 93453 (431-4) 93431 (426-8)
Quantity recalled1,333 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-0826-2013
FDA event ID
63786
Recalling firm
Unified Seafood, Los Angeles, CA
Classification
Class II
Status
Terminated
Recall initiated
23 Oct 2012
FDA classified
14 Dec 2012
Reported
26 Dec 2012
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Other Reasons
Product category
Tuna

Timeline

23 Oct 2012Recall initiated by company
14 Dec 2012Classified by FDA+52 days
26 Dec 2012Published 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

Unified Seafood Co is recalling Frozen Yellowfin Tuna Loin 3/5 due to possible contamination with Scombroid Toxin.

Product as listed by the FDA

Frozen Tuna Loins 3/5, 30lbs., UPC 8 29838 82310 7.

Where it was distributed

nationwide in the US: CA and WA and to Canada.

Nationwide CaliforniaWashington

Questions about this recall

Why was it recalled?

Unified Seafood Co is recalling Frozen Yellowfin Tuna Loin 3/5 due to possible contamination with Scombroid Toxin.

Which lots are affected?

Lot and (Code): 93514 (436-9) 93453 (431-4) 93431 (426-8)

Where was it sold?

nationwide in the US: CA and WA and to Canada.

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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