Hong Chang Hanryosued Anchovy Dashi: Un-eviscerated Fish Recall
Hong Chang Corporation recalls Hanryosued (F. Dashi Anchovy) 1.5kg packs due to un-eviscerated or partially eviscerated fish. Consumers should check UPCs 826546102745 and 826546102378.
Lower-risk recall
Un-eviscerated and/or partially eviscerated dried fish.
Contact the company
What happened, in plain English
Hong Chang Corporation is recalling Hanryosued (F. Dashi Anchovy) 1.5kg packs because they may contain un-eviscerated or partially eviscerated fish. This poses a risk of injury from sharp fish bones. Read more at govinfonow.com/recall/19857-hong-chang-hanryosued-anchovy-dashi-un-eviscerated-fish-recall.
Source Summary by GovInfoNow · govinfonow.com/recall/19857-hong-chang-hanryosued-anchovy-dashi-un-eviscerated-fish-recall · Updated October 7, 2026 · FDA enforcement record: FDA #F-0696-2018
Cite this page
“Hong Chang Hanryosued Anchovy Dashi: Un-eviscerated Fish Recall.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/19857-hong-chang-hanryosued-anchovy-dashi-un-eviscerated-fish-recall. Based on FDA recall #F-0696-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0696-2018%22&limit=1).
Why it’s dangerous
The product may contain fish that are not fully processed, meaning bones could be sharp and cause injury if eaten. This is a food safety issue related to improper evisceration during production.
Who’s affected
Anyone who purchased Hanryosued (F. Dashi Anchovy) 1.5kg packs with UPCs 826546102745 or 826546102378. People who eat the product may face injury from sharp fish bones.
How to tell if you have this one
Check for Hanryosued (F. Dashi Anchovy) 1.5kg packs with UPC codes 826546102745 or 826546102378. The product was sold in the U.S. and is a dried fish product.
- Brand
Hong Chang Corporation- Product
Hanryosued (F. Dashi Anchovy) 1.5kg x pack/carton UPC 826546102745, 826546102378- Category
Food
What to do — step by step
Check Product UPC
Look for UPC codes 826546102745 or 826546102378 on the package.
Where it went and when
Where it was distributed
Distributed in 6 states.
FDA distribution: “U.S. distribution to the following: CA., WA, TX, CO, HI, IL. No foreign distribution.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: California, Colorado, Hawaii, Illinois, Texas, Washington.
Recall timeline
FDA terminated this recall 41 days after the firm started it.
- Firm started the recall
- Published in FDA’s Enforcement Report
- FDA classified it Class I
- 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-0696-2018 (December 29, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0696-2018 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.