Summary
The FDA issued a Class III for Soybean Lecithin Powder Packaged in 44 lb. (20 kg.) boxes by Navada Imports. Reason: Undeclared peanut allergen.
Details
Source
Food Recall
External ID
F-0610-2023
Action Date
2023-03-22
Status
Terminated
Category
food
Product Description
Soybean Lecithin Powder Packaged in 44 lb. (20 kg.) boxes
Lot/Code Info: Navada Imports lot number: NI-SOYLECP-0222 Amitex Agro lot number: AAPPL/DOL/SOY/0802-22 Manufacture Date: February 08, 2022 Expiration Date: February 07, 2024 Navada Imports lot number: NI-SOYLECP-0422 Amitex Agro lot number: AAPPL/DOL/SOY/2504-22 Manufacture Date: April 25, 2022 Expiration Date: April 24, 2024
Quantity Affected: 575 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
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-0610-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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