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Sura Tanmen Hot and Sour Flavor Premium Japanese Noodles & Soup Base. Retail package net… Recalled: Soba sauce packet, which contains bonito, sardine, and mackerel (fish), was packed into S…

Sura Tanmen Hot and Sour Flavor Premium Japanese Noodles &… was recalled on August 4, 2026 in cooperation with the U.S. Food and Drug Administration because soba sauce packet, which contains bonito, sardine, and mackerel (fish), was packed into Sura Tanmen Hot and Sour Flavor ramen noodle…

Is my unit affected?

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

Model, lot & date codes to check

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

Units affected: 140 packages

Where it was sold: Distribute in HI.

Compare the codes above against the label on your product — usually on the bottom, the back panel, or the packaging. If your unit isn't listed, it is not part of this recall.

What's the hazard?

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.

Class I is the most serious FDA recall level: using or being exposed to the product could cause serious health problems or death.

Your remedy & how to claim it

Stop using the product. Return it to the place of purchase for a refund, or dispose of it. Contact the recalling firm with questions.

Contact: Recalling firm: H & U Inc. dba Sun Noodle

Not sure what you're entitled to? Read our guide: what to do if your product is recalled.

Official recall notice

Always confirm details on the official notice from the U.S. Food and Drug Administration before acting.

View official notice →

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