20 oz Garlic and 24 oz Garlic frozen pizza dough manufactured by It'll Be Pizza
Summary
The FDA issued a Class II for 20 oz Garlic and 24 oz Garlic frozen pizza dough manufactured by It'll Be Pizza by It'll Be Pizza, LLC.. Reason: Product may be contaminated with foreign object (debris from packaging)..
Details
Source
Food Recall
External ID
F-0201-2023
Action Date
2022-12-28
Status
Terminated
Category
food
Product Description
20 oz Garlic and 24 oz Garlic frozen pizza dough manufactured by It'll Be Pizza
Lot/Code Info: " 20 oz Garlic: 233944 " 24 oz Garlic: 233945; 233946
Quantity Affected: 1678 cases (total)
Reason for Recall
Product may be contaminated with foreign object (debris from packaging).
Distribution
ME, VT, MA, PA, NH
Type: Voluntary: Firm initiated
Recall Initiated: 2022-12-06
Company
Sanford, ME
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 13 food recalls issued in the same week, part of 204 food-related FDA actions this month.
It'll Be Pizza, LLC. has 7 FDA actions in our database, including 7 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 (It'll Be Pizza, LLC.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does It'll Be Pizza, LLC. have FDA actions?
It'll Be Pizza, LLC. has 7 FDA actions in our database, including 7 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0201-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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