Food Recall Check
Class I · High risk Terminated Initiated Oct 4, 2012 (14 years ago)

BUITONI brand Spinach & Portobello Mushroom All Natural Ravioli recall

Recalled by Nestle Prepared Foods Company · Haverhill, MA, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

BUITONI Spinach & Portobello Mushroom All Natural Ravioli may instead contain BUITONI Ravioli Shrimp and Lobster (undeclared allergens -shrimp and lobster)

Undeclared allergen: Shellfish

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

BUITONI brand Spinach & Portobello Mushroom All Natural Ravioli, packaged in an 18 oz. bag, frozen UPC code 24842-99186

Quantity: 323 cases/4 case (1292 bags)

Food: Leafy greens & salads

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.

Bag marked with a production code of 225451757 "best before" date of OCT 2013

Where it was sold

Nationwide.

FDA's distribution note: Nationwide

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 shellfish; 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
Nestle Prepared Foods Company
Initiated by
Voluntary: Firm initiated
Recall initiated
Oct 4, 2012
In FDA report of
Oct 31, 2012
Terminated
Apr 10, 2013
FDA recall number
F-0319-2013 · event 63370
Official record
FDA enforcement report search

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