Choshiya branded "SOFT TSUBOZUKE PREPARED MIX VEGETABLES" UPC# JANCODE 4582207535159
Summary
The FDA issued a Class I for Choshiya branded "SOFT TSUBOZUKE PREPARED MIX VEGETABLES" UPC# JANCODE 458220753 by AKT Trading Inc.. Reason: Various non-shelf stable packaged vegetables missing "Keep Refrigerated" statement on label..
Details
Source
Food Recall
External ID
F-0678-2025
Action Date
2025-04-09
Status
Terminated
Category
food
Product Description
Choshiya branded "SOFT TSUBOZUKE PREPARED MIX VEGETABLES" UPC# JANCODE 4582207535159
Lot/Code Info: Expiration: 07/29/2025
Quantity Affected: 800 cases (20 units per case)
Reason for Recall
Various non-shelf stable packaged vegetables missing "Keep Refrigerated" statement on label.
Distribution
Distribution for all products is limited to one direct account consignee (Tokyo Central)
Type: Voluntary: Firm initiated
Recall Initiated: 2025-02-18
Company
Torrance, 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 32 food recalls issued in the same week, part of 204 food-related FDA actions this month.
AKT Trading Inc. has 7 FDA actions in our database, including 7 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 (AKT Trading Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does AKT Trading Inc. have FDA actions?
AKT Trading Inc. has 7 FDA actions in our database, including 7 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0678-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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