FDA recall record
Vitanut Pro IC, 50 g
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, 2013. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
Vitanut Pro IC, 50 g
Reason
The product has the potential to be contaminated with Salmonella. The product was manufactured using peanut paste supplied by Sunland, Inc.
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.
Vitanut Pro IC, 50 g
Code information listed by FDA
Lot Code 2236
Distribution and firm information
Recalling firm listed by FDA: Breedlove Foods, Inc.
Firm location listed by FDA: Lubbock, TX, United States
Distribution reported by FDA: Product was exported to Columbia.
Product quantity listed by FDA: 1,469 cases (240 sachets/case)
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.