Class ITerminated in FDA datasetRecall initiated Jan 29, 2020

Nopalina Flax Seed Fiber Capsules

Recalling firm: Salud Natural Entrepreneur, Inc.

Why it was recalled

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…

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Nov 3, 2020.

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ProductNopalina Flax Seed Fiber Capsules, 120 count bottle, UPC 8 90523 00086 7
UPC890523000867

FDA code information

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

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Full FDA record and distribution details

Original product description

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

Extracted codes and context

TypeCode / valueContext
UPC890523000867Nopalina Flax Seed Fiber Capsules, 120 count bottle, UPC 8 90523 00086 7
best by10/7/21a 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
best by10/7/21 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
best by10/7/21 23.19.2C120#02 Best if used by 10/7/21 " Lot # 23.19.3C120#02 Best if used by 10/7/21
lot23.19.2C120 (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
lot23.19.3C120est 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

Original FDA recall 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.

Recall details

Recall number
F-0756-2020
Event ID
84812
FDA status
Terminated
Initiated
Jan 29, 2020
Reported
Mar 4, 2020
Classified
Feb 26, 2020
Terminated
Nov 3, 2020
Quantity
7111 bottles
Location
Waukegan, IL, United States
Initiation type
Voluntary: Firm initiated
Notification
Press Release

Where it was distributed

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/

FDA source record · F-0756-2020

Data updated September 16, 2026. View official FDA data ↗

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