RecallHawk
Class III Recall

Sunflower Lecithin Powder Packaged in 44 lb. (20 kg.) boxes

Navada Imports

Summary

The FDA issued a Class III for Sunflower Lecithin Powder Packaged in 44 lb. (20 kg.) boxes by Navada Imports. Reason: Undeclared peanut allergen.

Details

Source

Food Recall

External ID

F-0607-2023

Action Date

2023-03-22

Status

Terminated

Category

food

Product Description

Sunflower Lecithin Powder Packaged in 44 lb. (20 kg.) boxes

Lot/Code Info: Navada Imports lot number: NI-SUNLECP-0522 Amitex Agro lot number: AAPPL/DOL/SUN/0305-22 Manufacture Date May 03, 2022 Expiration Date: May 02, 2024

Quantity Affected: 221 cases

Reason for Recall

Undeclared peanut allergen

Distribution

Distributed to a distributor in MO and then further distributed nationwide to manufacturers.

Type: Voluntary: Firm initiated

Recall Initiated: 2023-02-02

Company

Navada Imports

Tinton Falls, NJ

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

Navada Imports has 4 FDA actions in our database, including 4 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 (Navada Imports) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Navada Imports have FDA actions?

Navada Imports has 4 FDA actions in our database, including 4 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0607-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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