Recall Radar

White Castle System recalls White Castle Chicken Slider Individual sandwiches packaged as two…: allergen risk

April 19, 2023 · White Castle System Class II

Class IIFDA’s middle class: use of the product may cause temporary or medically reversible adverse health consequences, or the chance of serious harm is remote.
Reason for the recallProduct packaged in incorrect labeling resulting in undeclared soy lecithin allergen

Find the official FDA enforcement report

Recall at a glance

Recalling company
White Castle System
Location
Columbus, OH
Reported by FDA
April 19, 2023
Recall started
April 4, 2023
Risk class
Class II
Status (latest data we have)
Terminated
Type
Voluntary: Firm initiated
Category
Meat and poultry
Reason type
Undeclared allergensLabeling and quality

Is my product affected?

Compare your product’s name, size and lot or date codes with the list below. A recall usually covers only specific codes.

  • White Castle Chicken Slider Individual sandwiches packaged as two sandwiches - 16 packages per case Unit Size 5.68oz/161g
    Quantity: 785 cases
    Codes: Batch No - CK278172K, CK278182K, CK278192K, CK278202K, CK278212K Lot No - WO0208102S10 Product No - 8298803826 Best By - 07/02/23

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.

What to do

If you have this product, check the codes above. FDA recall notices often tell consumers to stop eating the product and to return it or throw it away. Follow the company’s instructions and the official FDA information, and if you are unsure, do not eat it. If someone becomes ill after eating a recalled food, contact a healthcare professional. See FDA’s recalls and safety alerts for company announcements.

Frequently asked questions

What was recalled?

White Castle System recalled 1 product, including White Castle Chicken Slider Individual sandwiches packaged as two sandwiches - 16 packages per case Unit Size 5.68oz/161g.

Why was it recalled?

Product packaged in incorrect labeling resulting in undeclared soy lecithin allergen

What does Class II mean?

FDA’s middle class: use of the product may cause temporary or medically reversible adverse health consequences, or the chance of serious harm is remote.

Where was it sold or shipped?

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 this product?

Compare the product name, size and lot or date codes with the details on this page. FDA recall notices often tell you to stop eating the product and to return it or throw it away. Follow the company’s instructions and the official FDA information. If you are unsure, do not eat it.

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Sources

Data provided by the U.S. Food and Drug Administration (FDA) through openFDA, shown as published and not validated by this site. This site is independent and is not affiliated with or endorsed by FDA. It covers FDA-regulated foods; meat, poultry and egg products are regulated by USDA. Do not rely on this site for medical decisions: for health concerns contact a healthcare professional, and always follow the official notice and the company’s instructions. Terms and disclaimer.