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