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