Wegmans ITALIAN CLASSICS Organic BLUSH SAUCE
Reason Incorrect rear panel label was applied to jars of cream sauce which declared milk allergen
Wegmans Italian Classics Diavolo Pasta Sauce recall
Recalled by LiDestri Foods, Inc. · Fairport, NY, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Product may contain undeclared fish.
Undeclared allergen: Fish
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
Wegmans Italian Classics Diavolo Pasta Sauce 24 OZ
Quantity: 623 cases
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.
UPC: 077890222409 Lot Code #F0589 Best By 3/31/25
Where it was sold
District of Columbia Delaware Massachusetts Maryland North Carolina New Jersey New York Pennsylvania Virginia
FDA's distribution note: Delaware, District of Columbia, Maryland, Massachusetts, New Jersey, New York, North Carolina, Pennsylvania, and Virginia
Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. The risk from an undeclared allergen is to people allergic to fish; 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
- LiDestri Foods, Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- May 16, 2023
- In FDA report of
- Jun 28, 2023
- Terminated
- Aug 4, 2023
- FDA recall number
- F-0993-2023 · event 92354
- Official record
- FDA enforcement report search
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