Italiamo brand Melanzane alla Parmigiana pregratinate (Eggplant Parmesan) 450g UPC: 20456436. Frozen product. Packaged i
Summary
The FDA issued a Class II for Italiamo brand Melanzane alla Parmigiana pregratinate (Eggplant Parmesan) 450g U by Lidl US TRADING. Reason: Undeclared wheat and milk (foreign language labeling).
Details
Source
Food Recall
External ID
F-1457-2024
Action Date
2024-07-10
Status
Terminated
Category
food
Product Description
Italiamo brand Melanzane alla Parmigiana pregratinate (Eggplant Parmesan) 450g UPC: 20456436. Frozen product. Packaged in plastic tray with paper sleeve, 12 units in every case.
Lot/Code Info: Lot/batch #:23318 Best By Date: 05/2025
Quantity Affected: approximately 2,880 units
Reason for Recall
Undeclared wheat and milk (foreign language labeling)
Distribution
Distributed to distribution centers and stores in VA, MD, NC, GA, SC, PA, NJ, DE, NY, and Washington D.C.
Type: Voluntary: Firm initiated
Recall Initiated: 2024-06-11
Company
Arlington, VA
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 51 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Lidl US TRADING has 15 FDA actions in our database, including 15 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 (Lidl US TRADING) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Lidl US TRADING have FDA actions?
Lidl US TRADING has 15 FDA actions in our database, including 15 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1457-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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