Food Recall Check
Class III · Low risk Terminated Initiated Feb 2, 2023 (4 years ago)

Soybean Lecithin Powder Packaged in recall

Recalled by Navada Imports · Tinton Falls, NJ, United States

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

Undeclared peanut allergen

Undeclared allergen: Peanut

For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.

What was recalled

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

Quantity: 575 cases

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

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

Where it was sold

Nationwide.

Missouri

FDA's distribution note: Distributed to a distributor in MO and then further distributed nationwide to manufacturers.

Low risk, but check. Class III means the product is unlikely to make anyone ill but breaks an FDA rule, often a labeling one. If your package matches, the store will normally refund it. The risk from an undeclared allergen is to people allergic to peanut; for anyone else the product is generally not a safety concern. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Navada Imports
Initiated by
Voluntary: Firm initiated
Recall initiated
Feb 2, 2023
In FDA report of
Mar 22, 2023
Terminated
Sep 12, 2024
FDA recall number
F-0610-2023 · event 91660
Official record
FDA enforcement report search

Also recalled with it (3 more products)

FDA files each product of one recall action separately; these share the same FDA event.