Fish Ball, Frozen, 4 pieces per pack, 5lbs Wt. UPC# 810093891320
Summary
The FDA issued a Class I for Fish Ball, Frozen, 4 pieces per pack, 5lbs Wt. UPC# 810093891320 by MIN JIANG FOOD STORE INC DBA KOI KOI TRADING. Reason: Undeclared allergen ingredient (Wheat and Sesame).
Details
Source
Food Recall
External ID
H-0532-2026
Action Date
2026-03-04
Status
Terminated
Category
food
Product Description
Fish Ball, Frozen, 4 pieces per pack, 5lbs Wt. UPC# 810093891320
Lot/Code Info: Item# 27530 Expiration: 11/11/2027
Quantity Affected: 8,232 case
Reason for Recall
Undeclared allergen ingredient (Wheat and Sesame)
Distribution
Product was distributed to 50 consignees across the following states; CA, HI, TX, CO, GA, OR, NJ, WA. Product was primarily distributed to restaurants and retail grocery stores.
Type: Voluntary: Firm initiated
Recall Initiated: 2026-01-28
Company
Commerce, 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 27 food recalls issued in the same week, part of 204 food-related FDA actions this month.
MIN JIANG FOOD STORE INC DBA KOI KOI TRADING has 3 FDA actions in our database, including 3 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 (MIN JIANG FOOD STORE INC DBA KOI KOI TRADING) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does MIN JIANG FOOD STORE INC DBA KOI KOI TRADING have FDA actions?
MIN JIANG FOOD STORE INC DBA KOI KOI TRADING has 3 FDA actions in our database, including 3 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0532-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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