Shirakiku Buckwheat Noodles Yamaimo Soba With Concentration Soup Base, 435G SK, UPC…
Wismettac Asian Foods, INC recalled this product and the FDA reported the enforcement action on 30 October 2019 as Class II. The recall was initiated by the firm. Product label identifies bonito, but product dipping sauce actually contains skipjack tuna, yellowfin tuna, and bluefin tuna as well as does not state the general allergen name of fish.

The record
Every field below is published by the FDA in the openFDA food enforcement database. Check the FDA notice before acting on any recall: this page is a reading of the public record, not a substitute for it.
- Product
- Shirakiku Buckwheat Noodles Yamaimo Soba With Concentration Soup Base, 435G SK, UPC 074410455200 Distributed by Wismettac Asian Foods, Inc. Santa Fe Springs, CA 90670
- UPC
- 074410455200
- Reason for recall
- Product label identifies bonito, but product dipping sauce actually contains skipjack tuna, yellowfin tuna, and bluefin tuna as well as does not state the general allergen name of fish.
- Recalling firm
- Wismettac Asian Foods, INC
- Firm location
- Santa Fe Springs, California, United States
- Classification
- Class II
- Status
- Terminated
- Recall number
- F-0059-2020
- Quantity
- 7,789 packs
- Distribution
- U.S. distribution to the following: AK, AZ, CA, CO, IL, KS, MA, MI, MN, MO, NJ, NV, NY, OH, OR, PA, WA No foreign distribution.
- Initiated
- 18 September 2019
- Reported by FDA
- 30 October 2019
- Terminated
- 20 December 2019
- Firm notified by
- Letter
- Product codes
- All Codes
Reading this record
Five things about this record are not in the record itself, and each one changes how it should be read.
- Class II means the FDA judged a remote probability of serious harm, or a probability of temporary or medically reversible harm. The class is assigned by an agency health hazard evaluation under 21 CFR 7.41, not by the firm.
- The firm started this recall itself. Most FDA food recalls are voluntary, and a recall is a food safety plan working rather than failing. The circumstances in which the agency asks for one instead are set out in 21 CFR 7.45.
- This record is the only one the FDA opened for its recall event, so it covers a single product code.
- The recall ran for 3 months, from 18 September 2019 to termination on 20 December 2019. Termination means the agency judged that all reasonable effort had been made, under 21 CFR 7.55, and it says nothing about whether product remained in circulation.
- The distribution pattern names 15 states, and the FDA published the enforcement report 6 weeks after the firm began the recall.
- Recalls of a grain, flour or pasta product run a median of 6 months, so this one was shorter than usual for its category. Flour is a raw agricultural product that consumers treat as though it were cooked, which is the whole reason raw flour recalls exist: nothing in milling is a kill step, and the hazard only appears when somebody eats the dough.
Named in the distribution pattern: Arizona, California, Colorado, Illinois, Kansas, Massachusetts, Michigan, Minnesota, Missouri, New Jersey, Nevada, New York, Ohio, Oregon, Pennsylvania. Those pages count recalls by where the RECALLING FIRM sits, which is a different question from where this product went.
Filed under grains, flour and pasta and prepared meals and sandwiches. A product can sit in more than one.
Other grains, flour and pasta recalls
These are the closest records in the corpus: the same kind of food. Unlike the firm’s own records below, they come from different companies, which is what makes them a pattern rather than a history.
Other records from Wismettac Asian Foods, INC
The FDA opens one enforcement record per product code, so several of these are frequently one recall event. 30 other records name this firm.
All 31 records for Wismettac Asian Foods, INC
All 2019 recalls · All FDA food recall data
Behind every recall is a clause somebody has to produce evidence for at their next audit. Krolda maps supplier documents to the clause they satisfy in FSSC 22000, IFS Food and 21 CFR 117, and routes the corrective action when the evidence is missing.
Early accessRecall records come from the openFDA food enforcement API, published by the U.S. Food and Drug Administration in the public domain. Krolda adds the hazard classification and the clause mapping; neither is an FDA determination. Always check the FDA notice before acting on a recall.