CLASS I Food recall · Reported 26 Jul 2017 · FDA Enforcement Report

Pacific Wave Frozen Tuna Loins recalled by Unified Seafood Company

Unified Seafood is recalling Pacific Wave Frozen Tuna Loins, distributed in California, Hawaii. The recall was initiated on 16 Jun 2017 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLot: 701 Series/ Code: C1921-C2212
Quantity recalled250 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-2579-2017
FDA event ID
77572
Recalling firm
Unified Seafood, Los Angeles, CA
Classification
Class I
Status
Terminated
Recall initiated
16 Jun 2017
FDA classified
14 Jul 2017
Reported
26 Jul 2017
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Hepatitis A
Product category
Tuna

Timeline

16 Jun 2017Recall initiated by company
14 Jul 2017Classified by FDA+28 days
26 Jul 2017Published 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

Direct customer tested tuna loins and had a positive result for Hepatitis A.

Product as listed by the FDA

Pacific Wave Frozen Tuna Loins; 30# case. Imported by Unified Seafood Co., Inc. www.unifiedseafood.com

Where it was distributed

One location each in CA and HI; one location in MX

CaliforniaHawaii

Questions about this recall

Why was it recalled?

Direct customer tested tuna loins and had a positive result for Hepatitis A.

Which lots are affected?

Lot: 701 Series/ Code: C1921-C2212

Where was it sold?

One location each in CA and HI; one location in MX

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 I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

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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