RecallHawk
Class II Recall

Connie's Classic Thin Crust Cheese Pizza, Chicago's Finest. Net Wt 20.36 oz. (1lb 4.36 oz) 577g. UPC 0 75706-19104 8.

Palermo Villa, Inc

Summary

The FDA issued a Class II for Connie's Classic Thin Crust Cheese Pizza, Chicago's Finest. Net Wt 20.36 oz. ( by Palermo Villa, Inc. Reason: Foreign material (plastic).

Details

Source

Food Recall

External ID

F-0382-2025

Action Date

2025-01-15

Status

Terminated

Category

food

Product Description

Connie's Classic Thin Crust Cheese Pizza, Chicago's Finest. Net Wt 20.36 oz. (1lb 4.36 oz) 577g. UPC 0 75706-19104 8. Keep Refrigerated. Distributed by: Palermo Villa, nc. Milwaukee, WI 53208.

Lot/Code Info: Lot Number: MR199856

Quantity Affected: 1,728 pizzas

Reason for Recall

Foreign material (plastic)

Distribution

IL, MN, WI

Type: Voluntary: Firm initiated

Recall Initiated: 2024-12-11

Company

Palermo Villa, Inc

Milwaukee, WI

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 69 food recalls issued in the same week, part of 204 food-related FDA actions this month.

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 (Palermo Villa, Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Palermo Villa, Inc have FDA actions?

This is the only FDA action we have on record for Palermo Villa, Inc in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0382-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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