Nopalina Flax Seed Fiber (Salud Natural) – Contamination Risk (2020)
Class I: A situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death
Class I recall indicates potential for serious health consequences.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Nopalina Flax Seed Fiber in 1 and 2 lb bags, UPC 8 90523 00072 0 and 8 90523 00084 3
Brand
Salud Natural Entrepreneur, Inc.
Lot Codes / Batch Numbers
Nopalina Flax Seed Fiber (powder, 2 lb. bags) " Lot # 64.19/2*2Lb#52.1 Best if used by 10/21/21
Products Sold
Nopalina Flax Seed Fiber (powder, 1 lb. bags) " Lot # 62.19/1#52.1 Best if used by 10/7/21 " Lot # 62.19/2#52.1 Best if used by 10/7/21 " Lot # 64.19/2#52.1 Best if used by 10/21/21 " Lot # 64.19/3#52.1 Best if used by 10/21/21 " Lot # 65.19/1#52.1 Best if used by 10/24/21 " Lot # 65.19/2#52.1 Best if used by 10/24/21 Nopalina Flax Seed Fiber (powder, 2 lb. bags) " Lot # 64.19/2*2Lb#52.1 Best if used by 10/21/21
Salud Natural Entrepreneur, Inc. is recalling Nopalina Flax Seed Fiber in 1 and 2 lb bags, UPC 8 90523 00072 0 and 8 90523 00084 3 due to FDA sampling of senna leaves powder, an ingredient used to manufacture the Nopalina Flax Seed Fiber (powder) and Nopalina Flax Seed Fiber (capsules), . This is a Class I recall, indicating a high risk of serious health consequences. Based on FDA enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
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.
Recommended Action
Per FDA guidance
Consumers should stop using the product and contact the recalling firm or return it to the place of purchase.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 6, 2026