CK Egg Salad Sandwich, net wt. 6.7oz. Product is closed-face sandwich and ready to eat product. UPC 983644000097.
Summary
The FDA issued a Class II for CK Egg Salad Sandwich, net wt. 6.7oz. Product is closed-face sandwich and ready by Capitol Commissary LLC. Reason: Potential cross contact with sesame..
Details
Source
Food Recall
External ID
F-1057-2024
Action Date
2024-03-20
Status
Terminated
Category
food
Product Description
CK Egg Salad Sandwich, net wt. 6.7oz. Product is closed-face sandwich and ready to eat product. UPC 983644000097.
Lot/Code Info: Lot Codes: 24039, 24040, 24043, 24044. Best By Dates: Feb. 15, 2024; Feb. 16, 2024; Feb. 17, 2024; Feb.19, 2024; Feb. 20, 2024; and Feb. 21, 2024.
Quantity Affected: 52 units total
Reason for Recall
Potential cross contact with sesame.
Distribution
Distributed in Arizona, California, Idaho, Nevada, Oregon, Utah, and Washington.
Type: Voluntary: Firm initiated
Recall Initiated: 2024-02-14
Company
Caldwell, ID
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 52 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Capitol Commissary LLC has 6 FDA actions in our database, including 6 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 (Capitol Commissary LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Capitol Commissary LLC have FDA actions?
Capitol Commissary LLC has 6 FDA actions in our database, including 6 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1057-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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