CLASS I Food recall · Reported 31 Oct 2012 · FDA Enforcement Report

Buitoni Spinach & Portobello Mushroom All Natural Ravioli recalled

Nestle Prepared Foods is recalling Buitoni Spinach & Portobello Mushroom All Natural Ravioli, distributed nationwide in the US. The recall was initiated on 4 Oct 2012 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesBag marked with a production code of 225451757 "best before" date of OCT 2013

Quantity recalled323 cases/4 case (1292 bags)

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number: F-0319-2013
FDA event ID: 63370
Recalling firm: Nestle Prepared Foods, Haverhill, MA
Brand: Buitoni
Classification: Class I
Status: Terminated
Recall initiated: 4 Oct 2012
FDA classified: 19 Oct 2012
Reported: 31 Oct 2012
Type: Voluntary: Firm initiated
Customers notified by: Letter
Reason category: Undeclared Fish & Shellfish
Product category: Fish

Timeline

4 Oct 2012	Recall initiated by company
19 Oct 2012	Classified by FDA	+15 days
31 Oct 2012	Published in enforcement report	+12 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

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

Product as listed by the FDA

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

Where it was distributed

Nationwide

Questions about this recall

Why was it recalled?

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

Which lots are affected?

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

Where was it sold?

Nationwide

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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