RecallHawk
Class II Recall

LuLu Chinese Express, Sweet and Sour Shrimp w/ Fried Rice, Net Wt. 16 oz (1 lb), UPC 2393329006, packaged in plastic con

JX Restaurants, Inc.

Summary

The FDA issued a Class II for LuLu Chinese Express, Sweet and Sour Shrimp w/ Fried Rice, Net Wt. 16 oz (1 lb), by JX Restaurants, Inc.. Reason: Soy is missing from the "Contains" statement..

Details

Source

Food Recall

External ID

F-0433-2025

Action Date

2025-02-05

Status

Terminated

Category

food

Product Description

LuLu Chinese Express, Sweet and Sour Shrimp w/ Fried Rice, Net Wt. 16 oz (1 lb), UPC 2393329006, packaged in plastic container.

Lot/Code Info: Sell by 12/25/2023

Quantity Affected: 28, 16 oz containers

Reason for Recall

Soy is missing from the "Contains" statement.

Distribution

Distributed to one retail location in MO.

Type: Voluntary: Firm initiated

Recall Initiated: 2023-12-20

Company

JX Restaurants, Inc.

Maryland Heights, MO

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 47 food recalls issued in the same week, part of 204 food-related FDA actions this month.

JX Restaurants, Inc. has 2 FDA actions in our database, including 2 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 (JX Restaurants, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does JX Restaurants, Inc. have FDA actions?

JX Restaurants, Inc. has 2 FDA actions in our database, including 2 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0433-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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