Izzio Artisan Bakery, LLC Recall: Potential foreign material - plastic - F-1643-2024

🇺🇸 United States

1. July 20, 2024 - Recall initiated
2. August 14, 2024 - Reported by source

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-1643-2024

Event ID

95029

Status

Ongoing

Classification

Class II

Company

Izzio Artisan Bakery, LLC

Product description

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

Quantity

450 cases

Reason

Potential foreign material - plastic

Recall initiation date

July 20, 2024

Report date

August 14, 2024

Classification date

Not published in this source record

Termination date

Not terminated as of this source record

Distribution pattern

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

UPC, lot, and code information

Lot numbers are 24183C and 24183A UPC: 65708202951 3

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

E-Mail

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Other products recalled under this same event

This recall shares FDA event ID 95029 with 2 other product entries in Public Health Trace.

Responsible company: Izzio Artisan Bakery, LLC

Other recalls from Izzio Artisan Bakery, LLC

A map highlighting the states named in the source's distribution description.

Distributed No data published

Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.

Distribution map

State	Distributed
Illinois	1
Michigan	1
Texas	1
Ohio	1
New Jersey	1
Florida	1
Arizona	1

States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information. See FDA Enforcement Reports versus recall announcements for how that database differs from a press-release-style announcement.

New to reading a recall record? See how to read an FDA recall record and what recall statuses mean.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace: July 18, 2026 ET

Frequently asked questions

What does a Class II mean?

FDA classifies this recall as Class II. See how to read an FDA recall record (linked above) for what each classification level means.

Is this recall still active?

According to FDA, this recall's status is "Ongoing." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the responsible agency's published instructions, linked below -- recall guidance is set by that agency, not by Public Health Trace.

Official guidance and record verification

Public Health Trace does not provide medical advice -- review the linked official source below for current, authoritative information.

Compare the product name, brand, package size, UPC, lot code, and date information on your product with the official record to see whether it matches.

This is FDA's general Enforcement Report entry for this product -- Public Health Trace has not linked a separate FDA consumer announcement to this record.

Public Health Trace last retrieved this record on July 18, 2026.

Public Health Trace republishes FDA's recall record and does not provide disposal, return, cleaning, or other recall-action instructions -- review the official record and FDA's general recall guidance (linked below) for what to do.

View the official FDA record · General recall guidance from FDA

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.

• Email
• X / Twitter
• Facebook