RecallHawk
Class II Recall

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

DeIorio Foods, Inc.

Summary

The FDA issued a Class II for DeIorio Foods, Inc. brand Cafe Pizza Dough Sheet; Keep Frozen by DeIorio Foods, Inc.. Reason: Product contains conveyor belt pieces..

Details

Source

Food Recall

External ID

F-0795-2024

Action Date

2024-01-31

Status

Terminated

Category

food

Product Description

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

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

Quantity Affected: 510 cases. Each case contains 21, 24 oz, 14 inch diameter frozen flat pizza dough.

Reason for Recall

Product contains conveyor belt pieces.

Distribution

CA, NC, PA

Type: Voluntary: Firm initiated

Recall Initiated: 2024-01-05

Company

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

This was one of 85 food recalls issued in the same week, part of 204 food-related FDA actions this month.

DeIorio Foods, Inc. has 2 FDA actions in our database, including 2 recalls.

Frequently Asked Questions

What is a Class II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (DeIorio Foods, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does DeIorio Foods, Inc. have FDA actions?

DeIorio Foods, Inc. has 2 FDA actions in our database, including 2 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0795-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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