RecallHawk
Class III Recall

Item FLD1971, Stir Fried Dried Shrimp, distributed in plastic clamshell containers. Net wt. 0.165lb. The H-Mart label d

Lemonland Food Corp

Summary

The FDA issued a Class III for Item FLD1971, Stir Fried Dried Shrimp, distributed in plastic clamshell containe by Lemonland Food Corp. Reason: Soy Sauce is declared but Wheat is not declared..

Details

Source

Food Recall

External ID

F-0050-2025

Action Date

2024-10-23

Status

Terminated

Category

food

Product Description

Item FLD1971, Stir Fried Dried Shrimp, distributed in plastic clamshell containers. Net wt. 0.165lb. The H-Mart label declares: Shrimp, Sesame Oil, Soy Sauce, Corn Syrup, Salt

Lot/Code Info: Exp date 9/21/24

Quantity Affected: 10 packages

Reason for Recall

Soy Sauce is declared but Wheat is not declared.

Distribution

Distributed in WA

Type: Voluntary: Firm initiated

Recall Initiated: 2024-09-11

Company

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 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 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-0050-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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