Food, drugs, devices › Wismettac Asian Foods, Inc.
Food recall: Marutomo Dashi Soup Base, Item # #37402 Ingredients: Dried Shaved Skipjack Tuna, Fish Extract (Dried Skipjack Tuna, Salt
Wismettac Asian Foods, Inc. (Santa Fe Springs, CA) initiated this food recall on 22 Jul 2022; FDA lists 1 product record under event 90666, classified Class I.
FDA defines Class I as a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death. 38% of the 452 food enforcement events initiated in 2022 carry the same class.
Status: Terminated, terminated 15 Aug 2023. Initiation: voluntary: firm initiated. Wismettac Asian Foods, Inc. has 13 enforcement events on this register, with a median of 1 product record per event.
Recall classification reflects the relative degree of health hazard. Text in quotation marks is FDA's. openFDA export dated 28 Sep 2026.
Recalling firm
Wismettac Asian Foods, Inc., Santa Fe Springs, CA.
Reason for recall
"Undeclared allergens; wheat and soy."
Distribution
"U.S. distribution to the following: CA and NV. No foreign distribution."
Product records
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| F-1555-2022 | Marutomo Dashi Soup Base, Item # #37402 Ingredients: Dried Shaved Skipjack Tuna, Fish Extract (Dried Skipjack Tuna, Salt, Sea Bream Bone, Yeast Extract), Kelp Extract (Kelp Extract, Sorbitol, Maltitol, Hydrogenated Starch Hydrolysate (Cassava), Salt, Ethyl Alcohol, Kelp Product of Japan Distributed by Wismettac Asian… | 1,025 units | Class I | Terminated | 24 Aug 2022 |
Context
Other enforcement events for Wismettac Asian Foods, Inc.
All 13 events for Wismettac Asian Foods, Inc.
Questions and answers
Why was this food recalled?
FDA's record gives the reason for recall as: "Undeclared allergens; wheat and soy."
What does Class I mean?
FDA classifies recalls by relative degree of health hazard. Class I is a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death.
Where was the product distributed?
FDA's distribution pattern field reads: "U.S. distribution to the following: CA and NV. No foreign distribution."
Is the recall still ongoing?
FDA lists the status as Terminated; the termination date is 15 Aug 2023. "Terminated" means FDA has determined that all reasonable efforts to remove or correct the product have been made.
Where does this data come from?
openFDA enforcement reports (food, drug and device), CC0, export dated 28 Sep 2026. Text in quotation marks is FDA's. The FDA enforcement report linked above is authoritative.
Provenance
Source: openFDA food enforcement reports (CC0), export dated 28 Sep 2026; records grouped by FDA event number. The class shown for the event is the most severe class among its records. Errors in processing are corrected at the next build; see corrections.