RecallHawk
Class II Recall

5912MOD-CAU 11" Gluten Free Friendly Cauliflower Shell; Bulk packaged in a blue poly bag, within a corrugated box. 20 un

Deiorio Foods Inc

Summary

The FDA issued a Class II for 5912MOD-CAU 11" Gluten Free Friendly Cauliflower Shell; Bulk packaged in a blue by Deiorio Foods Inc. Reason: Product may be contaminated with foreign objects (white fragments of plastic, varying in length and width)..

Details

Source

Food Recall

External ID

F-0576-2025

Action Date

2025-03-05

Status

Terminated

Category

food

Product Description

5912MOD-CAU 11" Gluten Free Friendly Cauliflower Shell; Bulk packaged in a blue poly bag, within a corrugated box. 20 units per case; Product UPC: 074542659125; Master Case GTIN: 00074542659125

Lot/Code Info: Production Date: 27-DEC-24 Production Date: 07-JAN-25 Production Date: 08-JAN-25

Quantity Affected: 1701 cases

Reason for Recall

Product may be contaminated with foreign objects (white fragments of plastic, varying in length and width).

Distribution

TX, MD, WI, CA, CO, NC, AZ, ID, OR, OH, UT

Type: Voluntary: Firm initiated

Recall Initiated: 2025-01-24

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 20 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-0576-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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