CLASS I Food recall · Reported 13 Nov 2019 · FDA Enforcement Report

Teriyaki Grilled Calamari, (Grilled Squid recalled

Azuma Foods International Inc USA is recalling Teriyaki Grilled Calamari, (Grilled Squid with Teriyaki Sauce) Product # 51100, distributed in Hawaii. The recall was initiated on 23 Oct 2019 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLot 0033797
Quantity recalled96 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-0167-2020
FDA event ID
84145
Recalling firm
Azuma Foods International Inc USA, Hayward, CA
Classification
Class I
Status
Terminated
Recall initiated
23 Oct 2019
FDA classified
21 Nov 2019
Reported
13 Nov 2019
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Listeria
Product category
Sauces & Condiments

Timeline

23 Oct 2019Recall initiated by company
13 Nov 2019Published in enforcement report+21 days
21 Nov 2019Classified by FDA+8 days

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

Reason for recall

Direct Account randomly tested two products with presumptive positive results for Listeria monocytogenes.

Listeria monocytogenes can grow at refrigerator temperatures. Infection is most dangerous for pregnant women, newborns, older adults and people with weakened immune systems. Symptoms can appear up to 70 days after eating contaminated food.

Product as listed by the FDA

Teriyaki Grilled Calamari, (Grilled Squid with Teriyaki Sauce) Product # 51100; not for retail 10pkg/2.2 lbs. (1kg)/case Distributed by: Azuma Foods International, Inc., USA, Hayward, CA 94545 Product of Thailand

Where it was distributed

HI only

Hawaii

Questions about this recall

Why was it recalled?

Direct Account randomly tested two products with presumptive positive results for Listeria monocytogenes.

Which lots are affected?

Lot 0033797

Where was it sold?

HI only

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.

Other products in this recall event

3 other products · FDA event 84145

More recalls from Azuma Foods International Inc USA

All 5

Other Sauces & Condiments recalls

All 928