Marutomo Dashi Soup Base, Item # #37402 Ingredients: Dried Shaved Skipjack Tuna, Fish Extract (Dried Skipjack Tuna, Salt
Summary
The FDA issued a Class I for Marutomo Dashi Soup Base, Item # #37402 Ingredients: Dried Shaved Skipjack Tuna, by Wismettac Asian Foods, Inc.. Reason: Undeclared allergens; wheat and soy..
Details
Source
Food Recall
External ID
F-1555-2022
Action Date
2022-08-24
Status
Terminated
Category
food
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
Lot/Code Info: All Best Before dates distributed between July 1, 2021 through July 22, 2022.
Quantity Affected: 1,025 units
Reason for Recall
Undeclared allergens; wheat and soy.
Distribution
U.S. distribution to the following: CA and NV. No foreign distribution.
Type: Voluntary: Firm initiated
Recall Initiated: 2022-07-22
Company
Santa Fe Springs, CA
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 38 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Wismettac Asian Foods, Inc. has 12 FDA actions in our database, including 12 recalls.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Wismettac Asian Foods, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Wismettac Asian Foods, Inc. have FDA actions?
Wismettac Asian Foods, Inc. has 12 FDA actions in our database, including 12 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1555-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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