FDA recall record
Nopalina Flax Seed Fiber Capsules, 120 count bottle, UPC 8 90523 00086 7
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 November 3, 2020. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
Nopalina Flax Seed Fiber Capsules, 120 count bottle, UPC 8 90523 00086 7
Reason
FDA sampling of senna leaves powder, an ingredient used to manufacture the Nopalina Flax Seed Fiber (powder) and Nopalina Flax Seed Fiber (capsules), tested positive for three types of Salmonella including Salmonella Gaminara, Salmonella Kentucky, and Salmonella Oranienburg.
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.
Nopalina Flax Seed Fiber Capsules, 120 count bottle, UPC 8 90523 00086 7
Code information listed by FDA
Nopalina Flax Seed Fiber (capsules, 120 count) " Lot # 23.19 1C120#02 Best if used by 10/7/21 " Lot # 23.19.2C120#02 Best if used by 10/7/21 " Lot # 23.19.3C120#02 Best if used by 10/7/21
Distribution and firm information
Recalling firm listed by FDA: Salud Natural Entrepreneur, Inc.
Firm location listed by FDA: Waukegan, IL, United States
Distribution reported by FDA: Nopalina Flax Seed products are distributed throughout the United States and Puerto Rico via retail stores and the companys web site https://www.nopalinaonline.com/
Product quantity listed by FDA: 7111 bottles
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.