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Lower risk Food recall · FDA · Published December 22, 2017

AJC International recalls Early Dawn Whole Tilapia with sulfadiazine antibiotic

AJC International recalls Early Dawn Whole Tilapia IQF, Gutted & Scaled, Farm Raised, 40 lbs. (Size 550-750g or 750g+) due to sulfadiazine antibiotic contamination. Consumers should check lot numbers and contact the company for details.

🇺🇸 FDA recall #F-0563-2018FoodAJC International ›
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Recalling firmAJC International, Inc.1000 Abernathy Rd Ste 600 · Atlanta, GA 30328-5647
✎ GovInfoNow plain-language explainer

What happened, in plain English

AJC International has recalled Early Dawn Whole Tilapia IQF, Gutted & Scaled, Farm Raised, 40 lbs. (Size 550-750g or 750g+) because samples tested positive for the antibiotic sulfadiazine. This poses a health risk as sulfadiazine can cause adverse effects when consumed. Read more at govinfonow.com/recall/19890-ajc-international-recalls-early-dawn-whole-tilapia-with-sulfadiazine-antibiotic.

Source Summary by GovInfoNow · govinfonow.com/recall/19890-ajc-international-recalls-early-dawn-whole-tilapia-with-sulfadiazine-antibiotic · Updated October 7, 2026 · FDA enforcement record: FDA #F-0563-2018

Cite this page

“AJC International recalls Early Dawn Whole Tilapia with sulfadiazine antibiotic.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/19890-ajc-international-recalls-early-dawn-whole-tilapia-with-sulfadiazine-antibiotic. Based on FDA recall #F-0563-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0563-2018%22&limit=1).

Why it’s dangerous

Sulfadiazine is an antibiotic that can be harmful when consumed in contaminated food. The presence of this antibiotic in tilapia indicates potential contamination during production or handling, which may lead to adverse health effects.

Who’s affected

Consumers who purchased Early Dawn Whole Tilapia IQF, Gutted & Scaled, Farm Raised, 40 lbs. (Size 550-750g or 750g+) with lot number 1985507 from China. People who eat the product may be at risk of adverse effects from sulfadiazine.

How to tell if you have this one

Check for the product name 'Early Dawn Whole Tilapia IQF, Gutted & Scaled, Farm Raised, 40 lbs.' with size 550-750g or 750g+. Look for lot number 1985507 produced on 08/12/2017 with a best used by date of 02/12/2019.

  • Brand
    AJC International
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Identify the product name, size, and lot number to confirm if it matches the recalled items.

Where it went and when

Where it was distributed

Distributed in Pennsylvania.

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: yesPANew 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: not listedHITexas: not listedTXFlorida: not listedFL

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

States: Pennsylvania.

Recall timeline

FDA terminated this recall 2.3 years after the firm started it.

1. Firm started the recall: Dec 22, 201712. FDA classified it Class II: Jan 10, 201823. Published in FDA’s Enforcement Report: Jan 10, 201834. FDA terminated the recall: Apr 27, 2020420172020
  1. Firm started the recall
  2. FDA classified it Class II
  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-0563-2018 (December 22, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0563-2018 to see it in context.
  • Plain-language summary written by qwen3:4b on October 7, 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