Reel Fresh Yellowfin Tuna Cubes Recall: Hepatitis A Risk from Indonesia
Reel Fresh Yellowfin Tuna Hilo Cubes (15 lb. cases) from Indonesia tested positive for hepatitis A. Consumers should stop using these products due to food safety risk.
Stop using this now
Frozen raw tuna cubes from Indonesia tested positive for hepatitis A.
Contact the company
What happened, in plain English
Tropic Fish Hawaii, LLC recalled Reel Fresh Yellowfin Tuna Hilo Cubes from Indonesia after testing found hepatitis A. This poses a food safety risk as hepatitis A can cause serious illness. Read more at govinfonow.com/recall/21804-reel-fresh-yellowfin-tuna-cubes-recall-hepatitis-a-risk-from.
Source Summary by GovInfoNow · govinfonow.com/recall/21804-reel-fresh-yellowfin-tuna-cubes-recall-hepatitis-a-risk-from · Updated October 8, 2026 · FDA enforcement record: FDA #F-2268-2017
Cite this page
“Reel Fresh Yellowfin Tuna Cubes Recall: Hepatitis A Risk from Indonesia.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/21804-reel-fresh-yellowfin-tuna-cubes-recall-hepatitis-a-risk-from. Based on FDA recall #F-2268-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-2268-2017%22&limit=1).
Why it’s dangerous
Frozen raw tuna cubes from Indonesia tested positive for hepatitis A virus. Hepatitis A is a contagious liver infection that can cause severe illness, especially in unvaccinated people.
Who’s affected
Anyone who purchased Reel Fresh Yellowfin Tuna Hilo Cubes (15 lb. cases) from Indonesia. People with close contact with infected individuals are at higher risk.
How to tell if you have this one
Look for Reel Fresh Yellowfin Tuna Hilo Cubes in 15 lb. cases with UPC 664183001454. Products were manufactured in Indonesia and have lot codes 633671 or 5005125.
- Brand
Reel Fresh- Product
Yellowfin Tuna Hilo Cubes, Random cut. 15 lb. cases. (1 x 15 lb. bags per case) Brand name: Reel Fresh UPC- Category
Food
What to do — step by step
Stop Using Now
Immediately discard any Reel Fresh Yellowfin Tuna Hilo Cubes (15 lb. cases) with UPC 664183001454.
How this recall unfolded
Recall timeline
FDA terminated this recall 4 months after the firm started it.
- Firm started the recall
- FDA classified it Class I
- Published in FDA’s Enforcement Report
- 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-2268-2017 (May 1, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-2268-2017 to see it in context.
- Plain-language summary written by qwen3:4b on October 8, 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.