Class ITerminated in FDA datasetRecall initiated Jul 22, 2022

Marutomo Dashi Soup Base, Item # #37402

Recalling firm: Wismettac Asian Foods, Inc.

Why it was recalled

Undeclared allergens; wheat and soy.

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Aug 15, 2023.

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ProductMarutomo 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
Package size17.63 OZ
UPC074410374020

FDA code information

All Best Before dates distributed between July 1, 2021 through July 22, 2022.

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Full FDA record and distribution details

Original product description

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

Extracted codes and context

TypeCode / valueContext
UPC074410374020Japan 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

Original FDA recall reason

Undeclared allergens; wheat and soy.

Recall details

Recall number
F-1555-2022
Event ID
90666
FDA status
Terminated
Initiated
Jul 22, 2022
Reported
Aug 24, 2022
Classified
Aug 18, 2022
Terminated
Aug 15, 2023
Quantity
1,025 units
Location
Santa Fe Springs, CA, United States
Initiation type
Voluntary: Firm initiated
Notification
Letter

Where it was distributed

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

FDA source record · F-1555-2022

Data updated September 16, 2026. View official FDA data ↗

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