RecallHawk
Class II Recall

Izzio Everything Roll packaged in 12oz plastic bag, 6 rolls per bag - 16 bags per case.

Izzio Artisan Bakery, LLC

Summary

The FDA issued a Class II for Izzio Everything Roll packaged in 12oz plastic bag, 6 rolls per bag - 16 bags pe by Izzio Artisan Bakery, LLC. Reason: Potential foreign material - plastic.

Details

Source

Food Recall

External ID

F-1643-2024

Action Date

2024-08-14

Status

Ongoing

Category

food

Product Description

Izzio Everything Roll packaged in 12oz plastic bag, 6 rolls per bag - 16 bags per case.

Lot/Code Info: Lot numbers are 24183C and 24183A UPC: 65708202951 3

Quantity Affected: 450 cases

Reason for Recall

Potential foreign material - plastic

Distribution

Recalled product was shipped to 7 retail stores and 3 distribution centers in the following states. IL, MI, TX,OH,NJ,FL, and AZ.

Type: Voluntary: Firm initiated

Recall Initiated: 2024-07-20

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 200 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Izzio Artisan Bakery, LLC has 3 FDA actions in our database, including 3 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 (Izzio Artisan Bakery, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Izzio Artisan Bakery, LLC have FDA actions?

Izzio Artisan Bakery, LLC has 3 FDA actions in our database, including 3 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1643-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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