Recall Register

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

Class III FDA enforcement event 91660. Recall start date: . Status in the FDA record: Terminated. Termination date: .

Reason for recall, in the words of FDA

Undeclared peanut allergen

Class III, in the words of FDA

a situation in which use of or exposure to a violative product is not likely to cause adverse health consequences

Navada Imports started this food recall on 2 Feb 2023. The firm address in the FDA record is in Tinton Falls, NJ. FDA put the recall in Class III. FDA event 91660 has 4 product records. The first FDA enforcement report date is 22 Mar 2023. The record gives the status Terminated, with the termination date 12 Sep 2024.

It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.

FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on . openFDA export of .

Distribution

In the words of FDA.

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

Recalling firm

Navada Imports, Tinton Falls, NJ.

Recalling firm: The firm that the FDA record names for a recall.

FDA records how the recall started: Voluntary: Firm initiated.

Products

4 product records in the event.

FDA event 91660: product records
Recall numberProductQuantityClassStatusReport date
F-0607-2023Sunflower Lecithin Powder Packaged in 44 lb. (20 kg.) boxes221 casesClass IIITerminated22 Mar 2023
F-0608-2023Sunflower Lecithin Liquid Packaged in 2,200 lb. (1,000 kg.) totes20 totes and 96 oz. sampleClass IIITerminated22 Mar 2023
F-0609-2023Organic Sunflower Lecithin Powder Packaged in 44 lb. (20 kg.) boxes18 lb sampleClass IIITerminated22 Mar 2023
F-0610-2023Soybean Lecithin Powder Packaged in 44 lb. (20 kg.) boxes575 casesClass IIITerminated22 Mar 2023

openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports. Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.

Enforcement report: The FDA publication that lists recalls. It has one record for each product of a recall.

Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.

Class III: The lowest of the three FDA recall classes.

The event in context

Food events that started in 2023
478
Share of these events in Class III
13%
Product records in this event
4
Events of the firm on the register
1

Official channels

Cite this page

Recall Register. FDA enforcement event 91660. https://recallregister.com/fda/iii/91660/. Source: openFDA enforcement reports. Data through .

Sources

Source
openFDA food enforcement reports
Licence
CC0 1.0
Export date
28 Sep 2026
Newest FDA report date on the register
23 Sep 2026

FDA has one record for each product. This site puts the records with the same event number on one page. The class of the event is the highest class of its records. How the register is made. Report an error.

Questions

Where was the product distributed?
The FDA record gives this distribution: Distributed to a distributor in MO and then further distributed nationwide to manufacturers.
What quantity of product is in FDA event 91660?
The event has 4 product records. The first record gives this quantity: 221 cases
How did the recall start?
The FDA record says: Voluntary: Firm initiated
How many food recalls of 2023 have the same class?
13% of the 478 food events that started in 2023 are in Class III.