Item FLD1080A, Seasoned Radish, distributed in plastic clamshell containers, net wt. 0.365lb. The H-Mart label declares
Summary
The FDA issued a Class I for Item FLD1080A, Seasoned Radish, distributed in plastic clamshell containers, net by Lemonland Food Corp. Reason: Undeclared Crustacean (shrimp)..
Details
Source
Food Recall
External ID
F-0043-2025
Action Date
2024-10-23
Status
Terminated
Category
food
Product Description
Item FLD1080A, Seasoned Radish, distributed in plastic clamshell containers, net wt. 0.365lb. The H-Mart label declares: Radish, Red Pepper Powder, Malt Syrup, Salt, Anchovy, Sugar, Garlic, Ginger, Sesame.
Lot/Code Info: Expire date 9/21/2024
Quantity Affected: 30 packages
Reason for Recall
Undeclared Crustacean (shrimp).
Distribution
Distributed in WA
Type: Voluntary: Firm initiated
Recall Initiated: 2024-09-11
Company
Kent, WA
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 33 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 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 (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-0043-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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