CLASS II Food recall · Reported 19 Apr 2023 · FDA Enforcement Report
White Castle Chicken Slider Individual sandwiches packaged recalled
White Castle System is recalling White Castle Chicken Slider Individual sandwiches packaged as two sandwiches - 16, distributed in Florida, Georgia, Illinois, Kentucky, South Carolina, Tennessee. The recall was initiated on 4 Apr 2023 and the FDA has classified it as Class II.
Check your package
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-0714-2023
- FDA event ID
- 92057
- Recalling firm
- White Castle System, Columbus, OH
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 4 Apr 2023
- FDA classified
- 11 Apr 2023
- Reported
- 19 Apr 2023
- Type
- Voluntary: Firm initiated
- Customers notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Reason category
- Undeclared Soy
- Product category
- Ready Meals
Timeline
| 4 Apr 2023 | Recall initiated by company | |
| 11 Apr 2023 | Classified by FDA | +7 days |
| 19 Apr 2023 | Published in enforcement report | +8 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Product packaged in incorrect labeling resulting in undeclared soy lecithin allergen
Product as listed by the FDA
White Castle Chicken Slider Individual sandwiches packaged as two sandwiches - 16 packages per case Unit Size 5.68oz/161g
Where it was distributed
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.
Questions about this recall
Is White Castle Chicken Slider Individual sandwiches packaged as two sandwiches - 16 recalled?
Yes. White Castle System recalled White Castle Chicken Slider Individual sandwiches packaged as two sandwiches - 16 on 4 Apr 2023. The recall is Class II and its status is Terminated. Recall number F-0714-2023.
Why was it recalled?
Product packaged in incorrect labeling resulting in undeclared soy lecithin allergen
Which lots are affected?
Batch No - CK278172K, CK278182K, CK278192K, CK278202K, CK278212K Lot No - WO0208102S10 Product No - 8298803826 Best By - 07/02/23
Where was it sold?
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.
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 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
More recalls from White Castle System
All 2| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Food | CLASS I | White Castle Original Sliders recalled | White Castle System | Undeclared Allergens | IL, OH, TX |
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