HIGH RISK Terminated F-0756-2020

Nopalina Flax Seed Fiber Capsules, 120 count bottle, UPC 8 90523 00086 7

Recalled by Salud Natural Entrepreneur, Inc.

Classification

Class I — Dangerous or defective products that predictably could cause serious health problems or death.

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.

Product Details

Product Quantity

7111 bottles

Product Type

Food

Code Info

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

Voluntary/Mandated

Voluntary: Firm initiated

Distribution & Geography

Distribution Pattern

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/

Company Location

Waukegan, IL, 60085-5458

Timeline

Report Date

03/04/2020

Recall Initiated

01/29/2020

Classification Date

02/26/2020

Termination Date

11/03/2020

Source: U.S. Food & Drug Administration (FDA) — FDA Recalls

Last updated: July 13, 2026

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