CLASS II Food recall · Reported 5 Feb 2025 · FDA Enforcement Report

LuLu Chinese Express, Sweet and Sour Shrimp w/ Fried Rice recalled

JX Restaurants is recalling LuLu Chinese Express, Sweet and Sour Shrimp w/ Fried Rice, distributed in Missouri. The recall was initiated on 20 Dec 2023 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesSell by 12/25/2023
Quantity recalled28, 16 oz containers

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-0433-2025
FDA event ID
95445
Recalling firm
JX Restaurants, Maryland Heights, MO
Brand
LuLu
Classification
Class II
Status
Terminated
Recall initiated
20 Dec 2023
FDA classified
29 Jan 2025
Reported
5 Feb 2025
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Foreign Material
Product category
Shrimp

Timeline

20 Dec 2023Recall initiated by company
29 Jan 2025Classified by FDA+406 days
5 Feb 2025Published in enforcement report+7 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Soy is missing from the "Contains" statement.

Foreign material recalls cover pieces of metal, plastic, glass, wood or other objects that got into the product during processing and could cause injury if eaten.

Product as listed by the FDA

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

Where it was distributed

Distributed to one retail location in MO.

Missouri

Questions about this recall

Why was it recalled?

Soy is missing from the "Contains" statement.

Which lots are affected?

Sell by 12/25/2023

Where was it sold?

Distributed to one retail location in MO.

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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