Sura Tanmen Hot and Sour Flavor Premium Japanese Noodles recall
Recalled by H & U Inc. dba Sun Noodle
The product, as the FDA describes it: Sura Tanmen Hot and Sour Flavor Premium Japanese Noodles & Soup Base. Retail package net wt. 15.4oz. Product is ramen noodle kit which contains noodles and Soba soup packet. Item #05410 retail package, UPC 085315054108 Item #05410.1 cardboard box (12 packages per case), UPC 085315054105 Product is Perishable Frozen or Refrigerated and made by Sun Noodle Hawaii 1933 Colburn Street, Honolulu, HI
Why it was recalled
Soba sauce packet, which contains bonito, sardine, and mackerel (fish), was packed into Sura Tanmen Hot and Sour Flavor ramen noodle package kit, but fish species are not declared on finished product label.
The FDA has since closed this recall out, which means the company finished removing the product from sale. It is kept here because a closed recall still matters to anyone holding a package bought before it ended.
What to do if you have it
This is a labelling failure rather than spoiled food, so it matters entirely to whoever eats it. If nobody in your household reacts to what went undeclared here, the product is not dangerous to you, though you can still return it. If somebody does, treat every package from the affected run as unsafe no matter how much has already been eaten without incident.
How to tell whether your package is one of them
A recall covers particular production runs, not everything the company makes, so the codes decide it. These are the ones the FDA published. Match them against what is printed on your package, usually near the best-before date.
Production Lot: 1226183 Products will be dated for expiration according to their date of defrost by retailer or distributor in the following format: MM/DD
The details on record
| Recalling company | H & U Inc. dba Sun Noodle |
|---|---|
| Company location | Honolulu, HI |
| Where it was distributed | Distribute in HI. |
| How much was recalled | 140 packages |
| Recall started | August 4, 2026 |
| Published by the FDA | September 2, 2026 |
| Recall type | Voluntary: Firm initiated |
| How the company announced it | Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit |
| FDA recall number | H-1258-2026 |
Everything above comes from the FDA enforcement report for this recall. Read the official notice for the company's own wording, contact numbers, and any photographs of the packaging.
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