FDA recall, , High risk
Sura Tanmen Hot and Sour Flavor Premium Japanese Noodles & Soup Base
Sura Tanmen Hot and Sour Flavor ramen noodle kit may contain undeclared fish allergen, posing a risk of serious allergic reaction.
Recall ended Aug 27, 2026. Still check yours.
Summary by Recall Canary from the FDA notice
What happened
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.
What to do
If a code on your package is listed below:
- Consumers who have purchased Sura Tanmen with lot code 1226183 are urged not to consume the product and to return it to the original place of purchase for a full refund.
- Consumers with questions may contact Sun Noodle at (808) 841-5808, Monday – Saturdays from 8:00am HST – 3:30pm HST, or snohanacare@
sunnoodle.com. - Consumers with concerns about an allergic reaction should contact their healthcare provider.
Is yours affected?
Match the lot code and UPC listed under your product.
A UPC is the number printed under a barcode.
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
- 085315054105
- Lot code
- 1226183
- Recall number
- H-1258-2026
- Sura tanmen
- Item Number
- Unit
- 05410
- Case
- 05410.1
- Sura tanmen
- UPC
- Unit
- 085315054108
- Case
- 085315054105
- Sura tanmen
- Affected Lot Code
- Unit
- 1226183
- Case
- 1226183
- Sura tanmen
- Net Wt.
- Unit
- 15.4oz per package
- Case
- 12 packages per case. 11.75 lbs. per case
- Sura tanmen
- Type of Container
- Unit
- Individual Plastic Package
- Case
- Cardboard Box of 12 Packages
Label photos, 2
Recall details
- Company began the recall
- Sold in
Distribute in Hawaii.
- Company
- H & U Inc. dba Sun NoodleHonolulu, Hawaii
- Hazard
- Undeclared fish
- Risk
High risk
There is a reasonable chance that eating it could cause serious health problems or death.
FDA Class I recall · How risk is rated
- Event ID
- 99571
- Recall number
- H-1258-2026
- Quantity recalled
- 140 packages
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Announced by the company
Listed on Recall Canary
Added to FDA's Enforcement Report · Classified by FDA
Recall ended
In FDA's weekly enforcement report
Summary updated
