Sura Tanmen Hot and Sour Flavor Premium Japanese Noodles & Soup Base. Retail package net wt. 15.4oz. Product is ramen no
Summary
The FDA issued a Class I for Sura Tanmen Hot and Sour Flavor Premium Japanese Noodles & Soup Base. Retail pac by H & U Inc. dba Sun Noodle. 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 .
Details
Source
Food Recall
External ID
H-1258-2026
Action Date
2026-09-02
Status
Terminated
Category
food
Product Description
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
Lot/Code Info: 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
Quantity Affected: 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.
Distribution
Distribute in HI.
Type: Voluntary: Firm initiated
Recall Initiated: 2026-08-04
Company
Honolulu, HI
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 47 food recalls issued in the same week, part of 82 food-related FDA actions this month.
H & U Inc. dba Sun Noodle has 2 FDA actions in our database, including 2 recalls.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (H & U Inc. dba Sun Noodle) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does H & U Inc. dba Sun Noodle have FDA actions?
H & U Inc. dba Sun Noodle has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-1258-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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