RecallHawk
Class III Recall

Renata Plant-Based Suprema Pizza, frozen & vacuum packaged in plastic bags. Net wt: 420 gr (14.8 oz); UPC: 6 53467 38864

Mi Piace LLC

Summary

The FDA issued a Class III for Renata Plant-Based Suprema Pizza, frozen & vacuum packaged in plastic bags. Net by Mi Piace LLC. Reason: Undeclared soy allergen in frozen pizza.

Details

Source

Food Recall

External ID

F-0279-2022

Action Date

2021-12-15

Status

Ongoing

Category

food

Product Description

Renata Plant-Based Suprema Pizza, frozen & vacuum packaged in plastic bags. Net wt: 420 gr (14.8 oz); UPC: 6 53467 38864 0; Manufactured by Renata Restaurant, 626 SE Main St, Portland, OR 97214; Product label, "Contains Wheat, Milk, Nuts, Coconut"

Lot/Code Info: Lot Code 0113021

Quantity Affected: 804

Reason for Recall

Undeclared soy allergen in frozen pizza

Distribution

Product was distributed to a distributor in OR who further distributed to 13 New Seasons Market locations in OR and WA.

Type: Voluntary: Firm initiated

Recall Initiated: 2021-10-29

Company

Mi Piace LLC

Portland, OR

Context & Analysis

This is a Class III recall. Class III recalls involve products unlikely to cause adverse health consequences, but that violate FDA regulations.

This was one of 60 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Frequently Asked Questions

What is a Class III recall?

A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.

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 (Mi Piace LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Mi Piace LLC have FDA actions?

This is the only FDA action we have on record for Mi Piace LLC in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0279-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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