FDA recall record
Sunflower Lecithin Powder Packaged in 44 lb. (20 kg.) boxes
FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.
FDA listed a termination date of September 12, 2024. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
Sunflower Lecithin Powder Packaged in 44 lb. (20 kg.) boxes
Reason
Undeclared peanut allergen
Products involved
Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.
Sunflower Lecithin Powder Packaged in 44 lb. (20 kg.) boxes
Code information listed by FDA
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
Distribution and firm information
Recalling firm listed by FDA: Navada Imports
Firm location listed by FDA: Tinton Falls, NJ, United States
Distribution reported by FDA: Distributed to a distributor in MO and then further distributed nationwide to manufacturers.
Product quantity listed by FDA: 221 cases
Source
Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.
Official FDA openFDA food enforcement record
Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.