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FDA source record Class I Terminated

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 Extr...

Recall Date: 2022-07-22 Recalling Firm: Wismettac Asian Foods, Inc. Record Ref: F-1555-2022

FINDARECALL QUICK READ

What this record tells you

This FDA record concerns 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 Extr... and names Wismettac Asian Foods, Inc. as the recalling firm. Use the source fields below to narrow the match, then verify the exact item and current remedy on the issuing-agency page.

  • Firm: Wismettac Asian Foods, Inc.
  • Classification: Class I
  • Status: Terminated
  • Recall date: 2022-07-22
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Product Description & Identification

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 Foods, Inc. Santa Fe Springs, CA 90670 UPC 0 74410 37402 0 NET WT. 17.63 OZ (1.1 LB) 500g

Reason for Recall / Hazard Identified

Undeclared allergens; wheat and soy.

How to Check Whether Your Product Matches

A matching product name or photograph is not enough by itself. Compare every identifier available on your item or packaging with the official notice.

  1. Confirm the full product and brand or recalling-firm name.
  2. Compare package size, color, flavor, model, style, or configuration when listed.
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  4. Review the recall date and distribution information without assuming every seller is listed.
  5. Open the official FDA source below and follow its current instructions.

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Consumer Action Recorded in the Source

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Distribution & Affected States

U.S. distribution to the following: CA and NV. No foreign distribution.

Verify With the Issuing Agency

This record was last updated in our index on 2026-08-09 21:59:13 UTC. Because recall enforcement statuses and instructions evolve, always verify details directly with the issuing government agency.

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Record Transparency

Issuing agency
FDA
Source ID
F-1555-2022
Indexed update
2026-08-09 21:59:13 UTC
Official source
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