RecallHawk
Class II Recall

White Castle Chicken Slider Individual sandwiches packaged as two sandwiches - 16 packages per case Unit Size 5.68oz/161

White Castle System

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

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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