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Lower risk Food recall · FDA · Published October 23, 2019

Azuma Foods recalls Teriyaki Grilled Calam: Listeria risk in imported squid product

Azuma Foods recalls 10-pkg teriyaki grilled squid product due to Listeria monocytogenes detected in samples. Consumers should avoid eating this item to prevent potential foodborne illness.

🇺🇸 FDA recall #F-0167-2020FoodAzuma Foods ›
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Recalling firmAzuma Foods International Inc USA20201 Mack St · Hayward, CA 94545-1224
✎ GovInfoNow plain-language explainer

Azuma Foods is recalling teriyaki grilled squid products because lab tests found Listeria monocytogenes, a bacteria that can cause serious food poisoning. This recall affects products sold in the U.S. from Thailand. Read more at govinfonow.com/recall/16485-azuma-foods-recalls-teriyaki-grilled-calam-listeria-risk-in-imported.

Source Summary by GovInfoNow · govinfonow.com/recall/16485-azuma-foods-recalls-teriyaki-grilled-calam-listeria-risk-in-imported · Updated October 5, 2026 · FDA enforcement record: FDA #F-0167-2020

Cite this page

“Azuma Foods recalls Teriyaki Grilled Calam: Listeria risk in imported squid product.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/16485-azuma-foods-recalls-teriyaki-grilled-calam-listeria-risk-in-imported. Based on FDA recall #F-0167-2020 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0167-2020%22&limit=1).

The FDA announced on Oct. 23, 2019, that Azuma Foods International Inc USA voluntarily recalled Teriyaki Grilled Calamari due to potential Listeria monocytogenes contamination. The product was distributed only in Hawaii.

How to tell if you have it

  • Brand: Azuma Foods
  • Product: Teriyaki Grilled Calamari, (Grilled Squid with Teriyaki Sauce)
  • Product #: 51100
  • Lot: 0033797
  • Size: 10pkg/2.2 lbs. (1kg)/case
  • Distribution: HI only

The hazard

The FDA stated that direct account testing yielded presumptive positive results for Listeria monocytogenes in two randomly tested products. The recall is classified as Class I.

Context

GovInfoNow's records show Azuma Foods International Inc USA has 2 other recalls on record since Dec. 4, 2015. Other recent recalls of similar products include IQ Produce Enoki Mushrooms Recall: Listeria Contamination Risk (May 14, 2026), HEMU Enoki Mushrooms Recall: Listeria Contamination Risk (April 2, 2026), and HH Fresh Enoki Mushrooms Recall: Listeria Contamination Risk (May 11, 2026).

How to tell if you have this one

Check for the product code 51100 on the package. The item was distributed by Azuma Foods International, Inc. in the U.S. and made in Thailand with lot number 0033797.

  • Brand
    Azuma Foods
  • Category
    Food
FDA recall event · 4 products

All 4 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Classification
    Class I
  • Status
    Terminated
  • Distribution
    HI only
Recall numberProduct, codes & lotsQuantity
F-0166-2020Frozen Ika Popo (Sugata Yaki); Product # 51106 16 pkg/0.46 lbs (210g)/case; Lot 00337978 cases
F-0167-2020Teriyaki 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; Lot 003379796 cases
F-0168-2020Salmon Misozuke; Seasoned Atlantic Salmon Product # 51104; Not For retail 10 pkg/5 pc(2.75 lbs./1.25 kg)/case Distributed by: Azuma Foods International, Inc., U.S.A. Hayward, CA 64545 Product of Thailand; Lot 003379738 cases
F-0169-2020Frozen Saba Misozuke; (seasoned Mackerel) Product # 51108, Not for Retail 12 pkg/5pc(1.76lbs./800g)/ case Distributed by: Azuma Foods International, Inc., U.S.A. Hayward, CA Product of Thailand; Lot 00337978 cases
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Look for product code 51100 on the package to confirm if it's recalled.

Where it went and when

Where it was distributed

Distributed in Hawaii.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: not listedWIMichigan: not listedMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: yesHITexas: not listedTXFlorida: not listedFL

FDA distribution: “HI only” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Hawaii.

Recall timeline

FDA terminated this recall 2 months after the firm started it.

1. Firm started the recall: Oct 23, 201912. Published in FDA’s Enforcement Report: Nov 13, 201923. FDA classified it Class I: Nov 21, 201934. FDA terminated the recall: Dec 27, 201942019
  1. Firm started the recall
  2. Published in FDA’s Enforcement Report
  3. FDA classified it Class I
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #F-0167-2020 (October 23, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0167-2020 to see it in context.
  • Plain-language summary written by qwen3:4b on October 5, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA