CLASS II Food recall · Reported 31 Jan 2024 · FDA Enforcement Report

Cafe Pizza Dough Sheet recalled by DeIorio Foods

DeIorio Foods is recalling Cafe Pizza Dough Sheet, distributed in California, North Carolina, Pennsylvania. The recall was initiated on 5 Jan 2024 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesBest if used by date: 02/16/2024, batches L1 B051 through L1 B074
Quantity recalled510 cases. Each case contains 21, 24 oz, 14 inch diameter frozen flat pizza dough.

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-0795-2024
FDA event ID
93811
Recalling firm
DeIorio Foods, Utica, NY
Brand
Inc
Classification
Class II
Status
Terminated
Recall initiated
5 Jan 2024
FDA classified
25 Jan 2024
Reported
31 Jan 2024
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Other Reasons
Product category
Frozen Pizza

Timeline

5 Jan 2024Recall initiated by company
25 Jan 2024Classified by FDA+20 days
31 Jan 2024Published in enforcement report+6 days

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

Reason for recall

Product contains conveyor belt pieces.

Product as listed by the FDA

DeIorio Foods, Inc. brand Cafe Pizza Dough Sheet; Keep Frozen

Where it was distributed

CA, NC, PA

CaliforniaNorth CarolinaPennsylvania

Questions about this recall

Why was it recalled?

Product contains conveyor belt pieces.

Which lots are affected?

Best if used by date: 02/16/2024, batches L1 B051 through L1 B074

Where was it sold?

CA, NC, PA

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 II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

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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