Recall · openFDA Food Enforcement

Nopalina Flax Seed Fiber Capsules, 120 count bottle, UPC 8…: FDA Recall F-0756-2020

Agency action: Jan 29, 2020Record ID: F-0756-2020
View official source ↗

What happened

Original notice title

Nopalina Flax Seed Fiber Capsules, 120 count bottle, UPC 8 90523 00086 7, recall F-0756-2020

From the archived source record

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.

What the official notice says to do

Check the original notice for the instructions that apply to the named product, company, and affected lots.

Read the official notice →

Status and source details

Status recorded in the archive
Terminated
FDA recall classification
Class I
Recall initiated by
Voluntary: Firm initiated
Report date
Mar 4, 2020
Termination date in the archive
Nov 3, 2020
Source checked
Jul 16, 2026
Record revision
c56f74a4e21b

This is a dated record. Its current status may have changed since the source was captured. A record applies to its stated scope; it is not a safety rating for every product from a company.

Sources, dates, and coverage →

What is affected

Product
Nopalina Flax Seed Fiber Capsules, 120 count bottle, UPC 8 90523 00086 7
Company
Salud Natural Entrepreneur, Inc.
Lot / identifier
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
Market / distribution
Nopalina Flax Seed products are distributed throughout the United States and Puerto Rico via retail stores and the company s web site https://www.nopalinaonline.com/