FDA Recall United States Terminated Historical recordClass I
JX Restaurants, Inc.
- Product
- LuLu Chinese Express Korean Noodles (Japchae) w/ Vegetables.…
- Published
- October 18, 2023
- Distribution
- MO
JX Restaurants, Inc. Recall: Soy is missing from the "Contains" statement.
United States
TerminatedClass II
- Company
- JX Restaurants, Inc.
- Product
- LuLu Chinese Express, Sweet and Sour Shrimp w/ Fried Rice, N…
- Recall date
- December 20, 2023
- Terminated
- March 21, 2025
- Source
- FDA
Reason for recall
Soy is missing from the "Contains" statement.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| LuLu Chinese Express, Sweet and Sour Shrimp w/ Fried Rice, Net Wt. 16 oz (1 lb), UPC 2393329006, packaged in plastic container. | 2393329006 | 28, 16 oz containers | Sell by 12/25/2023 |
Distribution
- Distributed to one retail location in MO.
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0433-2025
- Event ID
- 95445
- Status
- Terminated
- Classification
- Class II
- Company
- JX Restaurants, Inc.
- Product description
- LuLu Chinese Express, Sweet and Sour Shrimp w/ Fried Rice, Net Wt. 16 oz (1 lb), UPC 2393329006, packaged in plastic container.
- Quantity
- 28, 16 oz containers
- Reason
- Soy is missing from the "Contains" statement.
- Recall initiation date
- December 20, 2023
- Report date
- February 5, 2025
- Classification date
- Not published in this source record
- Termination date
- March 21, 2025
- Distribution pattern
- Distributed to one retail location in MO.
- UPC, lot, and code information
- UPC 2393329006; Sell by 12/25/2023
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: JX Restaurants, Inc.
Other recalls from JX Restaurants, Inc.
A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| State | Distributed |
|---|---|
| Missouri | 1 |
States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class II mean?
A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.
Is this recall still active?
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
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