Aldi Mixed Sourdough loaf. A single 24oz loaf packaged into plastic bag, 12 loaves per case.
Summary
The FDA issued a Class II for Aldi Mixed Sourdough loaf. A single 24oz loaf packaged into plastic bag, 12 loav by Izzio Artisan Bakery, LLC. Reason: Potential foreign material - plastic.
Details
Source
Food Recall
External ID
F-1644-2024
Action Date
2024-08-14
Status
Ongoing
Category
food
Product Description
Aldi Mixed Sourdough loaf. A single 24oz loaf packaged into plastic bag, 12 loaves per case.
Lot/Code Info: Lot numbers 24184B, 24183B, 24184C, 24183C, 24184A UPC: EVSD 4099100291254
Quantity Affected: 9500 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
Louisville, CO
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-1644-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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