White Castle Chicken Slider Individual sandwiches packaged as two sandwiches - 16 packages per case Unit Size 5.68oz/161
Summary
The FDA issued a Class II for White Castle Chicken Slider Individual sandwiches packaged as two sandwiches - 1 by White Castle System. Reason: Product packaged in incorrect labeling resulting in undeclared soy lecithin allergen.
Details
Source
Food Recall
External ID
F-0714-2023
Action Date
2023-04-19
Status
Terminated
Category
food
Product Description
White Castle Chicken Slider Individual sandwiches packaged as two sandwiches - 16 packages per case Unit Size 5.68oz/161g
Lot/Code Info: Batch No - CK278172K, CK278182K, CK278192K, CK278202K, CK278212K Lot No - WO0208102S10 Product No - 8298803826 Best By - 07/02/23
Quantity Affected: 785 cases
Reason for Recall
Product packaged in incorrect labeling resulting in undeclared soy lecithin allergen
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.
Type: Voluntary: Firm initiated
Recall Initiated: 2023-04-04
Company
Columbus, OH
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 45 food recalls issued in the same week, part of 204 food-related FDA actions this month.
White Castle System has 2 FDA actions in our database, including 2 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (White Castle System) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does White Castle System have FDA actions?
White Castle System has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0714-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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