Class ITerminatedVoluntary: Firm initiated
H & U Inc. dba Sun Noodle: food recall H-1258-2026
H & U Inc. dba Sun Noodle of Honolulu, HI recalled Sura Tanmen Hot and Sour Flavor Premium Japanese Noodles & Soup Base. Retail package net wt. 15.4oz. Product is ramen… Reason: 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 listed it as Class I in its Enforcement Report dated Sep 2, 2026; distribution: Hawaii.
Record status as published: Terminated (terminated Aug 27, 2026). openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- Product
- 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
- Product quantity
- 140 packages
- Reason for recall
- 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.
- Codes, lots and dates on the package
- 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
- Distribution pattern
- Distribute in HI.
- Recalling firm
- H & U Inc. dba Sun Noodle, Honolulu, HI
- Classification
- Class I — the FDA uses this class for a situation in which there is a reasonable probability that using or being exposed to the product will cause serious adverse health consequences or death.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Aug 4, 2026 |
| Classified by the FDA | Aug 21, 2026 |
| Published in the Enforcement Report | Sep 2, 2026 |
| Terminated | Aug 27, 2026 |
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-1258-2026 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
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