Food Recall Check
Class II · Moderate risk Terminated Initiated Jun 11, 2024 (2 years ago)

Italiamo brand Melanzane alla Parmigiana pregratinate recall

Recalled by Lidl US TRADING · Arlington, VA, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Undeclared wheat and milk (foreign language labeling)

Undeclared allergens: Milk Wheat

For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.

What was recalled

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.

Quantity: approximately 2,880 units

Food: Cheese

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

Lot/batch #:23318 Best By Date: 05/2025

Where it was sold

Delaware Georgia Maryland North Carolina New Jersey New York Pennsylvania South Carolina Virginia Washington

FDA's distribution note: Distributed to distribution centers and stores in VA, MD, NC, GA, SC, PA, NJ, DE, NY, and Washington D.C.

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. The risk from an undeclared allergen is to people allergic to milk, wheat; for anyone else the product is generally not a safety concern. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Lidl US TRADING
Initiated by
Voluntary: Firm initiated
Recall initiated
Jun 11, 2024
In FDA report of
Jul 10, 2024
Terminated
Sep 26, 2024
FDA recall number
F-1457-2024 · event 94822
Official record
FDA enforcement report search

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