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Stop using now Food recall · FDA · Published June 14, 2017

Pacific Wave Yellow Fin Tuna Recall: Hepatitis A Risk

P & E Foods recalls Pacific Wave Yellow Fin Tuna loins due to potential Hepatitis A contamination. Check lot codes C1921-C2212.

🇺🇸 FDA recall #F-2398-2017FoodPacific Wave ›
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Recalling firmP & E Foods Inc3077 Koapaka St Ste 202 · Honolulu, HI 96819-5105
✎ GovInfoNow plain-language explainer

What happened, in plain English

P & E Foods Inc is recalling Pacific Wave Yellow Fin Tuna loins because laboratory testing confirmed a positive result for Hepatitis A. The affected product consists of 30 lb. cases imported from Indonesia by Unified Seafood Co., Inc. This recall involves only two cases distributed to one customer in Hawaii for overseas distribution. Read more at govinfonow.com/recall/20798-pacific-wave-yellow-fin-tuna-recall-hepatitis-a-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/20798-pacific-wave-yellow-fin-tuna-recall-hepatitis-a-risk · Updated October 11, 2026 · FDA enforcement record: FDA #F-2398-2017

Cite this page

“Pacific Wave Yellow Fin Tuna Recall: Hepatitis A Risk.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/20798-pacific-wave-yellow-fin-tuna-recall-hepatitis-a-risk. Based on FDA recall #F-2398-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-2398-2017%22&limit=1).

Why it’s dangerous

Hepatitis A is a viral infection that affects the liver and can cause serious illness. The presence of the virus in the tuna loins poses a direct health risk if the product is consumed without proper cooking or handling precautions, although the record does not specify further details on transmission.

Who’s affected

The recall is limited to a single customer in Hawaii who received the product for overseas distribution. Consumers are unlikely to have this specific item, but anyone with these tuna loins should treat them as unsafe.

How to tell if you have this one

Look for Pacific Wave Yellow Fin Tuna loins in 30 lb. cases. The product is from Indonesia and imported by Unified Seafood Co., Inc. You must check the lot code; the recalled items have Lot 701 Series with codes ranging from C1921 to C2212.

  • Brand
    Pacific Wave
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Stop using the product

    Do not consume or distribute the recalled Pacific Wave Yellow Fin Tuna loins due to Hepatitis A contamination.

  2. Check lot codes

    Verify if your product has Lot 701 Series with codes C1921 through C2212.

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: “One customer in HI for overseas distribution.” 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: Jun 14, 201712. FDA classified it Class I: Jul 13, 201723. Published in FDA’s Enforcement Report: Jul 19, 201734. FDA terminated the recall: Aug 22, 201742017
  1. Firm started the recall
  2. FDA classified it Class I
  3. Published in FDA’s Enforcement Report
  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-2398-2017 (June 14, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-2398-2017 to see it in context.
  • Plain-language summary written by qwen3.6:35b-a3b on October 11, 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