Kagome Take Out Tonkatsu Sauce STOCK: #24274 40 packets (8g) in a plastic bag. 15 bags in a box
Summary
The FDA issued a Class I for Kagome Take Out Tonkatsu Sauce STOCK: #24274 40 packets (8g) in a plastic bag. 1 by Mutual Trading Company Inc.. Reason: Undeclared allergen; soy..
Details
Source
Food Recall
External ID
F-0744-2023
Action Date
2023-04-19
Status
Terminated
Category
food
Product Description
Kagome Take Out Tonkatsu Sauce STOCK: #24274 40 packets (8g) in a plastic bag. 15 bags in a box
Lot/Code Info: Lot: 2020.7.29 or before this date
Quantity Affected: 393 cases
Reason for Recall
Undeclared allergen; soy.
Distribution
U.S. distribution to the following: CA, AZ, NZ, TX, NM, OK, HI No foreign distribution.
Type: Voluntary: Firm initiated
Recall Initiated: 2023-03-17
Company
El Monte, 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 45 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Mutual Trading Company Inc. has 4 FDA actions in our database, including 4 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 (Mutual Trading Company Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Mutual Trading Company Inc. have FDA actions?
Mutual Trading Company Inc. has 4 FDA actions in our database, including 4 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0744-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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