RecallHawk
Class II Recall

Item FLD1015A, Stewed Lotus Root, distributed in plastic clamshell containers, net wt. 0.315lb. The H-Mart label declar

Lemonland Food Corp

Summary

The FDA issued a Class II for Item FLD1015A, Stewed Lotus Root, distributed in plastic clamshell containers, n by Lemonland Food Corp. Reason: Soybean Sauce is declared but Wheat and Fish (Anchovy) are not declared..

Details

Source

Food Recall

External ID

F-0045-2025

Action Date

2024-10-23

Status

Terminated

Category

food

Product Description

Item FLD1015A, Stewed Lotus Root, distributed in plastic clamshell containers, net wt. 0.315lb. The H-Mart label declares: Lotus Root, Salt, Soy Sauce, Corn Syrup

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

Quantity Affected: 25 packages

Reason for Recall

Soybean Sauce is declared but Wheat and Fish (Anchovy) are not declared.

Distribution

Distributed in WA

Type: Voluntary: Firm initiated

Recall Initiated: 2024-09-11

Company

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 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 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-0045-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

Want to know the moment something like this happens?

Get alerts for food

Related Actions