Lower riskFood recall · FDA · Published July 22, 2022
Wismettac Marutomo Dashi Soup Base Recall: Undeclared Wheat and Soy Allergens
Wismettac Asian Foods recalls Marutomo Dashi Soup Base (Item #37402) due to undeclared wheat and soy allergens. This product was distributed from July 1, 2021 to July 22, 2022. Consumers should check labels and contact the company for details.
“Wismettac Marutomo Dashi Soup Base Recall: Undeclared Wheat and Soy Allergens.” GovInfoNow, updated August 6, 2026. https://govinfonow.com/recall/12556-wismettac-marutomo-dashi-soup-base-recall-undeclared-wheat-and-soy. Based on FDA recall #F-1555-2022 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1555-2022%22&limit=1).
The FDA announced on July 22, 2022, that Wismettac Asian Foods, Inc. voluntarily recalled Marutomo Dashi Soup Base due to undeclared wheat and soy allergens. Consumers should check their products for the specified UPC and best-before dates.
How to tell if you have it
Brand: Wismettac
Product: Marutomo Dashi Soup Base
Item #: #37402
UPC: 0 74410 37402 0
Best Before dates: July 1, 2021 through July 22, 2022
Distribution: California and Nevada
The hazard
The product contains undeclared allergens: wheat and soy. The FDA classified this as a Class I recall.
Context
GovInfoNow's records show Wismettac Asian Foods, Inc. has had 12 other recalls on record since May 16, 2019. Recent similar recalls include the Wismettac Curvee Puffs Corn Puff Snack recall on January 16, 2025, and the Wismettac Korean Seaweed Recall on October 9, 2024. Other recent recalls of similar products include the Sliced Korean Halibut with Soy Sauce recall (July 1, 2026), the Good & Gather Sesame Teriyaki Chicken Recall (April 24, 2026), and the Kettle Cuisine Minestrone Soup Recall (May 19, 2026).
How to tell if you have this one
Check for the product name 'Marutomo Dashi Soup Base' and item number #37402. The product was distributed between July 1, 2021 and July 22, 2022 with a net weight of 17.63 ounces.
Look for the item number #37402 and the distribution dates between July 1, 2021 and July 22, 2022.
Where it went and when
Where it was distributed
Distributed in California and Nevada.
Listed by the agency
Not listed
FDA distribution: “U.S. distribution to the following: CA and NV. No foreign distribution.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: California, Nevada.
Recall timeline
FDA terminated this recall 13 months after the firm started it.
1Firm started the recall
2FDA classified it Class I
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #F-1555-2022 (July 22, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1555-2022 to see it in context.
Plain-language summary written by qwen3:4b on August 6, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.