Nopalina Flax Seed Fiber Capsules — Class I food recall F-0756-2020
Terminated recall by Salud Natural Entrepreneur, Inc., reported 2020-03-04, distributed nationwide. FDA sampling of senna leaves powder, an ingredient used to manufacture the Nopalina Flax Seed Fiber (powder) a
| Recall number | F-0756-2020 |
|---|---|
| Product type | Food |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Salud Natural Entrepreneur, Inc., Waukegan, IL, United States |
| Recall initiated | 2020-01-29 |
| Classified | 2020-02-26 |
| Reported by FDA | 2020-03-04 |
| Terminated | 2020-11-03 |
| Distributed | Nationwide (US) |
| Quantity | 7,111 bottles |
| Reason classes | microbial contamination |
| Pathogens | salmonella |
| UPC / GTIN / UDI-DI | 00890523000867 |
| Lot numbers | 23.19 |
| Expiration dates | 2021-10-07 |
Product
Nopalina Flax Seed Fiber Capsules, 120 count bottle, UPC 8 90523 00086 7
Reason for recall
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/F-0756-2020. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.