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Salud Natural Entrepreneur, Inc. 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.

United States

TerminatedClass I

Company
Salud Natural Entrepreneur, Inc.
Product
Nopalina Flax Seed Fiber in 1 and 2 lb bags, UPC 8 90523 000…
Recall date
January 29, 2020
Terminated
November 3, 2020
Source
FDA

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.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Nopalina Flax Seed Fiber in 1 and 2 lb bags, UPC 8 90523 00072 0 and 8 90523 00084 3 Not published in this source record 20511 bags 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

Distribution

  • 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/

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0755-2020
Event ID
84812
Status
Terminated
Classification
Class I
Company
Salud Natural Entrepreneur, Inc.
Product description
Nopalina Flax Seed Fiber in 1 and 2 lb bags, UPC 8 90523 00072 0 and 8 90523 00084 3
Quantity
20511 bags
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 initiation date
January 29, 2020
Report date
March 4, 2020
Classification date
Not published in this source record
Termination date
November 3, 2020
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/
UPC, lot, and code information
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
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Press Release
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Other products recalled under this same event

This recall shares FDA event ID 84812 with 1 other product entry in Public Health Trace.

FDA Recall United States Terminated Historical recordClass I

Salud Natural Entrepreneur, Inc.

Product
Nopalina Flax Seed Fiber Capsules, 120 count bottle, UPC 8 9…
Published
March 4, 2020
Distribution
Nopalina Flax Seed products are distribu…

View recall →

Responsible company: Salud Natural Entrepreneur, Inc.

Other recalls from Salud Natural Entrepreneur, Inc.

FDA Recall United States Terminated Historical recordClass I

Salud Natural Entrepreneur, Inc.

Product
Nopalina Flax Seed Fiber Capsules, 120 count bottle, UPC 8 9…
Published
March 4, 2020
Distribution
Nopalina Flax Seed products are distribu…

View recall →

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class I mean?

A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.