FDA Recall United States Terminated 2026 recordClass I
White Castle System
- Product
- White Castle Original Sliders, Net Wt. 6.35 oz. (180g), pack…
- Published
- January 28, 2026
- Distribution
- Multiple states
White Castle System Recall: Product packaged in incorrect labeling resulting in undeclared soy lecithin allergen
United States
TerminatedClass II
- Company
- White Castle System
- Product
- White Castle Chicken Slider Individual sandwiches packaged a…
- Recall date
- April 4, 2023
- Terminated
- May 18, 2023
- Source
- FDA
Reason for recall
Product packaged in incorrect labeling resulting in undeclared soy lecithin allergen
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| White Castle Chicken Slider Individual sandwiches packaged as two sandwiches - 16 packages per case Unit Size 5.68oz/161g | Not published in this source record | 785 cases | Batch No - CK278172K, CK278182K, CK278192K, CK278202K, CK278212K Lot No - WO0208102S10 Product No - 8298803826 Best By - 07/02/23 |
Distribution
- Florida
- Georgia
- Illinois
- Kentucky
- South Carolina
- Tennessee *Product is sent to vending customers. Product is only sold in vending machines and not at retail locations.
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0714-2023
- Event ID
- 92057
- Status
- Terminated
- Classification
- Class II
- Company
- White Castle System
- Product description
- White Castle Chicken Slider Individual sandwiches packaged as two sandwiches - 16 packages per case Unit Size 5.68oz/161g
- Quantity
- 785 cases
- Reason
- Product packaged in incorrect labeling resulting in undeclared soy lecithin allergen
- Recall initiation date
- April 4, 2023
- Report date
- April 19, 2023
- Classification date
- Not published in this source record
- Termination date
- May 18, 2023
- Distribution pattern
- Florida, Georgia, Illinois, Kentucky, South Carolina, Tennessee *Product is sent to vending customers. Product is only sold in vending machines and not at retail locations.
- UPC, lot, and code information
- Batch No - CK278172K, CK278182K, CK278192K, CK278202K, CK278212K Lot No - WO0208102S10 Product No - 8298803826 Best By - 07/02/23
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: White Castle System
Other recalls from White Castle System
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?
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