Stir-Fried Kimchi distributed in un-labeled plastic containers 12oz. Containers were then labeled at H-mart, G-mart, or
Summary
The FDA issued a Class II for Stir-Fried Kimchi distributed in un-labeled plastic containers 12oz. Containers by Lemonland Food Corp. Reason: Stir-Fried Kimchi was recalled due to undeclared Fish (Anchovy), Shrimp, Wheat, and Sesame Oil..
Details
Source
Food Recall
External ID
F-0665-2023
Action Date
2023-04-05
Status
Terminated
Category
food
Product Description
Stir-Fried Kimchi distributed in un-labeled plastic containers 12oz. Containers were then labeled at H-mart, G-mart, or M2M retail store.
Lot/Code Info: Feb. 16, 2023 to Feb. 23, 2023.
Quantity Affected: 12oz. containers = 39.17 lb.
Reason for Recall
Stir-Fried Kimchi was recalled due to undeclared Fish (Anchovy), Shrimp, Wheat, and Sesame Oil.
Distribution
Distributed in Washington
Type: Voluntary: Firm initiated
Recall Initiated: 2023-02-23
Company
Kent, WA
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 66 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Lemonland Food Corp has 44 FDA actions in our database, including 44 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
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 (Lemonland Food Corp) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Lemonland Food Corp have FDA actions?
Lemonland Food Corp has 44 FDA actions in our database, including 44 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0665-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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