RecallHawk
Class III Recall

IO Inspired Organics brand Organic Raw Walnut Halves & Pieces; 7oz plastic tubs; 9 packages per wholesale case; retail U

Lipari Foods Operating Company, LLC.

Summary

The FDA issued a Class III for IO Inspired Organics brand Organic Raw Walnut Halves & Pieces; 7oz plastic tubs; by Lipari Foods Operating Company, LLC.. Reason: undeclared walnuts in ingredient and contains statement.

Details

Source

Food Recall

External ID

F-1459-2023

Action Date

2023-08-23

Status

Terminated

Category

food

Product Description

IO Inspired Organics brand Organic Raw Walnut Halves & Pieces; 7oz plastic tubs; 9 packages per wholesale case; retail UPC 863669740065, Lipari #943469

Lot/Code Info: batch number 21202306A; expiration 6/21/2024

Quantity Affected: 855 units

Reason for Recall

undeclared walnuts in ingredient and contains statement

Distribution

AL, FL, IL, IN, KY, MI, NY, OH, PA, WI, and WY

Type: Voluntary: Firm initiated

Recall Initiated: 2023-08-01

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

Lipari Foods Operating Company, LLC. has 9 FDA actions in our database, including 9 recalls.

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

How often does Lipari Foods Operating Company, LLC. have FDA actions?

Lipari Foods Operating Company, LLC. has 9 FDA actions in our database, including 9 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1459-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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