Rakkyo (scallions) distributed in un-labeled plastic containers 8oz and/or 12oz. Containers were then labeled at H-mart
Summary
The FDA issued a Class III for Rakkyo (scallions) distributed in un-labeled plastic containers 8oz and/or 12oz. by Lemonland Food Corp. Reason: Rakkyo was removed because the firm provided the updated ingredients statement to consignees. Product does not contain any allergens..
Details
Source
Food Recall
External ID
F-0671-2023
Action Date
2023-04-05
Status
Terminated
Category
food
Product Description
Rakkyo (scallions) distributed in un-labeled plastic containers 8oz and/or 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 = 28.12 lb; 8oz containers = Firm did not report quantity.
Reason for Recall
Rakkyo was removed because the firm provided the updated ingredients statement to consignees. Product does not contain any allergens.
Distribution
Distributed in Washington
Type: Voluntary: Firm initiated
Recall Initiated: 2023-02-23
Company
Kent, WA
Context & Analysis
This is a Class III recall. Class III recalls involve products unlikely to cause adverse health consequences, but that violate FDA regulations.
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 III recall?
A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.
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-0671-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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