Go Backs
HomeCategoriesStatesCheck Your Home
Go Backs

Track product recalls and safety alerts from CPSC, FDA, NHTSA, and USDA. Stay informed and keep your family safe.

Browse

  • Categories
  • States
  • Check Your Home
  • Risk Levels

Agencies

  • CPSC
  • FDA Food
  • FDA Drug
  • FDA Device
  • FDA Veterinary
  • NHTSA
  • USDA

Company

  • About
  • FAQ
  • Contact
  • Terms of Service
  • Privacy Policy
Buy Me a Coffee

Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

ยฉ 2026 Go Backs. All rights reserved.

Low RiskFDA Food
Food & Beverages/Packaged & Processed

Navada Imports Lecithin Products Recalled for Undeclared Peanut Allergen

Agency Publication Date: March 14, 2023
Share:
Sign in to monitor this recall

Summary

Navada Imports is recalling approximately 834 units of Sunflower and Soybean Lecithin products because they contain an undeclared peanut allergen. The recall includes 44-pound boxes of lecithin powder and 2,200-pound totes of liquid lecithin. These products were distributed to a distributor in Missouri and then sent to manufacturers nationwide. To date, no incidents or injuries related to this recall have been reported.

Risk

People who have an allergy or severe sensitivity to peanuts run the risk of a serious or life-threatening allergic reaction if they consume these products. Because peanuts are not listed on the label, consumers may be unaware of the danger.

What You Should Do

  1. This recall affects Sunflower Lecithin Powder, Sunflower Lecithin Liquid, Organic Sunflower Lecithin Powder, and Soybean Lecithin Powder sold in 44 lb. (20 kg.) boxes or 2,200 lb. (1,000 kg.) totes under the Navada Imports brand.
  2. Check your product packaging for Navada Imports lot numbers such as NI-SUNLECP-0522, NI-SUNLECL-0822, or NI-SOYLECP-0222 with expiration dates between February and August 2024. See the Affected Products section below for the full list of affected codes.
  3. Return the product to the place of purchase for a full refund, throw it away, or contact the manufacturer for further instructions.
  4. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) for additional questions regarding this recall.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Return the product to the place of purchase for a full refund, or contact the manufacturer or supplier for further instructions
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Throw the product away.

Affected Products

Product: Sunflower Lecithin Powder (44 lb. box)
Variants: Powder
Lot Numbers:
NI-SUNLECP-0522 (Exp May 02, 2024)

Amitex Agro lot number: AAPPL/DOL/SUN/0305-22; Manufactured May 03, 2022

Product: Sunflower Lecithin Liquid (2,200 lb. tote)
Variants: Liquid
Lot Numbers:
NI-SUNLECL-0822 (Exp August 01, 2024)
NI-SUNLECL-0622 (Exp June 11, 2024)

Associated Amitex Agro lot numbers: NI-SUNLECL-0822 and AAPPL/SFL/SUN/1206-22

Product: Organic Sunflower Lecithin Powder (44 lb. box)
Variants: Organic, Powder
Lot Numbers:
NI-OSUNLP-0522 (Exp May 02, 2024)

Amitex Agro lot number: AAPPL/ORG/SUNP/0305-22; Manufactured May 03, 2022

Product: Soybean Lecithin Powder (44 lb. box)
Variants: Soy, Powder
Lot Numbers:
NI-SOYLECP-0222 (Exp February 07, 2024)
NI-SOYLECP-0422 (Exp April 24, 2024)

Associated Amitex Agro lot numbers: AAPPL/DOL/SOY/0802-22 and AAPPL/DOL/SOY/2504-22

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 91660
Status: Resolved
Manufacturer: Navada Imports
Sold By: manufacturers
Manufactured In: United States
Units Affected: 4 products (221 cases; 20 totes and 96 oz. sample; 18 lb sample; 575 cases)
Distributed To: Nationwide

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.