RecallHawk
Class I Recall

Jacksons Turkey and Cheese Sandwich, net wt. 6.7oz. Product is closed-face sandwich and ready to eat product. UPC 98364

Capitol Commissary LLC

Summary

The FDA issued a Class I for Jacksons Turkey and Cheese Sandwich, net wt. 6.7oz. Product is closed-face sand by Capitol Commissary LLC. Reason: Undeclared sesame..

Details

Source

Food Recall

External ID

F-1056-2024

Action Date

2024-03-20

Status

Terminated

Category

food

Product Description

Jacksons Turkey and Cheese Sandwich, net wt. 6.7oz. Product is closed-face sandwich and ready to eat product. UPC 983642601562. The sandwich label declares "Ingredients: Multigrain Bread ***Contains: Wheat, Milk, Soy."

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: 1382 units

Reason for Recall

Undeclared sesame.

Distribution

Distributed in Arizona, California, Idaho, Nevada, Oregon, Utah, and Washington.

Type: Voluntary: Firm initiated

Recall Initiated: 2024-02-14

Company

Context & Analysis

This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

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 I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

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-1056-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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